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@@ -0,0 +1,68034 @@
+
+
+
+
+ 01:02:2022 11:15
+ MOP is the molecular process ontology. It contains the molecular processes that underlie the name reaction ontology RXNO, for example cyclization, methylation and demethylation.
+ MOP
+
+ 1.2
+
+
+
+
+
+
+
+
+
+
+
+
+ definition
+
+
+
+
+
+
+
+
+
+
+
+
+
+ imported from
+
+
+
+
+
+
+
+
+
+
+
+
+
+ FORMULA
+
+
+
+
+
+
+
+
+ IUPAC NAME
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ synonym_type_property
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ has_alternative_id
+
+
+
+
+
+
+
+ database_cross_reference
+
+
+
+
+
+
+
+ has_exact_synonym
+
+
+
+
+
+
+
+ has_narrow_synonym
+
+
+
+
+
+
+
+ has_obo_format_version
+
+
+
+
+
+
+
+ has_obo_namespace
+
+
+
+
+
+
+
+ has_related_synonym
+
+
+
+
+
+
+
+ has_synonym_type
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ BFO:0000055
+ realizes
+
+
+
+
+
+
+
+ BFO:0000057
+ has_participant
+
+
+
+
+
+
+
+
+ BFO:0000077
+ has participant beginning to exist
+
+
+
+
+
+
+
+
+ BFO:0000078
+ has participant ceasing to exist
+
+
+
+
+
+
+
+ BFO:0000117
+ has occurrent part
+
+
+
+
+
+
+
+ BFO:0000119
+ has profile
+
+
+
+
+
+
+
+ BFO:0000132
+ part of occurrent
+
+
+
+
+
+
+
+ BFO:0000133
+ process profile of
+
+
+
+
+
+
+
+ BFO:0000162
+ has disposition at all times
+
+
+
+
+
+
+
+
+ x is_catalysis_of y if and only if x positively_regulates y and the positive regulation works by providing a more kinetically-favourable route across the energy landscape from the reactants of y to the products of y.
+ MOP:0000769
+ is_catalysis_of
+
+
+
+
+ x is_catalysis_of y if and only if x positively_regulates y and the positive regulation works by providing a more kinetically-favourable route across the energy landscape from the reactants of y to the products of y.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+ x positively regulates y if and only if the progression of x increases the frequency, rate or extent of y
+ RO:0002213
+ positively_regulates
+
+
+
+
+
+
+
+
+
+
+
+
+ BFO:0000015
+ process
+
+
+
+
+
+
+
+ BFO:0000016
+ disposition
+
+
+
+
+
+
+
+
+ BFO:0000144
+ process profile
+
+
+
+
+
+
+
+
+ CHEBI:15378
+ hydron
+
+
+
+
+
+
+
+
+ CHEBI:18379
+ nitrile
+
+
+
+
+
+
+
+
+ CHEBI:22221
+ acyl group
+
+
+
+
+
+
+
+
+ CHEBI:23367
+ molecular entity
+
+
+
+
+
+
+
+ CHEBI:24431
+ chemical entity
+
+
+
+
+
+
+
+
+ A defined linked collection of atoms or a single atom within a molecular entity.
+ group
+ Gruppe
+ Rest
+ groupe
+ grupo
+ grupos
+ CHEBI:24433
+ group
+
+
+
+
+ group
+ IUPAC:
+
+
+
+
+
+ Gruppe
+ ChEBI:
+
+
+
+
+ Rest
+ ChEBI:
+
+
+
+
+ groupe
+ IUPAC:
+
+
+
+
+ grupo
+ IUPAC:
+
+
+
+
+ grupos
+ IUPAC:
+
+
+
+
+
+
+
+
+ CHEBI:24636
+ proton
+
+
+
+
+
+
+
+
+ CHEBI:26519
+ radical
+
+
+
+
+
+
+
+
+ CHEBI:29233
+ deuteron
+
+
+
+
+
+
+
+
+ isothiocyanatido
+ isothiocyanato
+ -NCS
+ CNS
+ SCN-
+ CHEBI:29441
+ isothiocyanato group
+
+
+
+
+ -NCS
+ IUPAC:
+
+
+
+
+ CNS
+ ChEBI:
+
+
+
+
+
+ SCN-
+ IUPAC:
+
+
+
+
+ isothiocyanatido
+ IUPAC:
+
+
+
+
+
+ isothiocyanato
+ IUPAC:
+
+
+
+
+
+
+
+
+
+ isoselenocyanatido
+ isoselenocyanato
+ -NCSe
+ CNSe
+ SeCN-
+ CHEBI:29444
+ isoselenocyanato group
+
+
+
+
+ isoselenocyanatido
+ IUPAC:
+
+
+
+
+
+ isoselenocyanato
+ IUPAC:
+
+
+
+
+
+ -NCSe
+ IUPAC:
+
+
+
+
+ CNSe
+ ChEBI:
+
+
+
+
+
+ SeCN-
+ IUPAC:
+
+
+
+
+
+
+
+
+ isocyanatido
+ isocyanato
+ -NCO
+ CNO
+ OCN-
+ CHEBI:29810
+ isocyanato group
+
+
+
+
+ isocyanatido
+ IUPAC:
+
+
+
+
+
+ isocyanato
+ IUPAC:
+
+
+
+
+
+ -NCO
+ IUPAC:
+
+
+
+
+ CNO
+ ChEBI:
+
+
+
+
+
+ OCN-
+ IUPAC:
+
+
+
+
+
+
+
+
+ CHEBI:32877
+ primary amine
+
+
+
+
+
+
+
+
+ CHEBI:32955
+ epoxide
+
+
+
+
+
+
+
+
+ CHEBI:33246
+ inorganic group
+
+
+
+
+
+
+
+
+ CHEBI:33247
+ organic group
+
+
+
+
+
+
+
+
+ CHEBI:33595
+ cyclic compound
+
+
+
+
+
+
+
+
+ CHEBI:33641
+ olefin
+
+
+
+
+
+
+
+
+ CHEBI:33823
+ enol
+
+
+
+
+
+
+
+
+ A macromolecule is a molecule of high relative molecular mass, the structure of which essentially comprises the multiple repetition of units derived, actually or conceptually, from molecules of low relative molecular mass.
+ CHEBI:33839
+ macromolecule
+
+
+
+
+
+
+
+
+ CHEBI:36342
+ subatomic particle
+
+
+
+
+
+
+
+
+ Any molecular entity consisting of more than one atom.
+ CHEBI:36357
+ polyatomic entity
+
+
+
+
+
+
+
+
+ CHEBI:36586
+ carbonyl compound
+
+
+
+
+
+
+
+
+ pseudohalide group
+ halogenoid group
+ pseudohalido group
+ pseudohalogen group
+ CHEBI:36823
+ pseudohalo groups
+
+
+
+
+ pseudohalide group
+ IUPAC:
+
+
+
+
+
+ halogenoid group
+ ChEBI:
+
+
+
+
+ pseudohalido group
+ ChEBI:
+
+
+
+
+ pseudohalogen group
+ IUPAC:
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ azido
+ -N3
+ N3
+ N3-
+ CHEBI:36825
+ azido group
+
+
+
+
+ azido
+ IUPAC:
+
+
+
+
+
+ -N3
+ IUPAC:
+
+
+
+
+ N3
+ ChEBI:
+
+
+
+
+
+ N3-
+ IUPAC:
+
+
+
+
+
+
+
+
+ isocyanido
+ isocyano
+ -NC
+ CN
+ CN-
+ CHEBI:36826
+ isocyano group
+
+
+
+
+ isocyanido
+ IUPAC:
+
+
+
+
+
+ isocyano
+ IUPAC:
+
+
+
+
+
+ -NC
+ IUPAC:
+
+
+
+
+ CN
+ ChEBI:
+
+
+
+
+
+ CN-
+ IUPAC:
+
+
+
+
+
+
+
+
+ isotellurocyanatido
+ isotellurocyanato
+ -NCTe
+ CNTe
+ TeCN-
+ CHEBI:36827
+ isotellurocyanato group
+
+
+
+
+ isotellurocyanatido
+ IUPAC:
+
+
+
+
+
+ isotellurocyanato
+ IUPAC:
+
+
+
+
+
+ -NCTe
+ IUPAC:
+
+
+
+
+ CNTe
+ ChEBI:
+
+
+
+
+
+ TeCN-
+ IUPAC:
+
+
+
+
+
+
+
+
+ CHEBI:37838
+ carboacyl group
+
+
+
+
+
+
+
+
+ A macromolecule derived from one species of (real, implicit or hypothetical) monomer.
+ CHEBI:37997
+ homopolymer
+
+
+
+
+
+
+
+
+ CHEBI:39141
+ Brønsted acid
+
+
+
+
+
+
+
+
+ CHEBI:39142
+ Brønsted base
+
+
+
+
+
+
+
+
+ CHEBI:39143
+ Lewis acid
+
+
+
+
+
+
+
+
+ CHEBI:39144
+ Lewis base
+
+
+
+
+
+
+
+
+ CHEBI:40574
+ acetyl group
+
+
+
+
+
+
+
+
+ formyl group
+
+
+
+
+
+
+
+
+ CHEBI:43176
+ hydroxy group
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ CHEBI:36824
+ CHEBI:48818
+ MSDchem:CN
+ cyanido
+ cyano
+ -C#N
+ -CN
+ CN
+ CYANIDE GROUP
+ NC-
+ carbonitrile group
+ CHEBI:48819
+ cyano group
+
+
+
+
+ MSDchem:CN
+ MSDchem
+
+
+
+
+ cyanido
+ IUPAC:
+
+
+
+
+
+ cyano
+ IUPAC:
+
+
+
+
+
+ -C#N
+ IUPAC:
+
+
+
+
+ -CN
+ IUPAC:
+
+
+
+
+ CN
+ ChEBI:
+
+
+
+
+
+ CYANIDE GROUP
+ MSDchem:
+
+
+
+
+ NC-
+ IUPAC:
+
+
+
+
+ carbonitrile group
+ ChEBI:
+
+
+
+
+
+
+
+
+ CHEBI:51100
+ sulfonyl groups
+
+
+
+
+
+
+
+
+ CHEBI:51142
+ amino groups
+
+
+
+
+
+
+
+
+ CHEBI:51144
+ nitrogen group
+
+
+
+
+
+
+
+
+
+ CHEBI:51870
+ boryl group
+
+
+
+
+
+
+
+
+ Any molecule or ion capable of binding to a central metal atom to form coordination complexes.
+ Wikipedia:Ligand
+ chebi_ontology
+ ligands
+ CHEBI:52214
+
+ ligand
+
+
+
+
+ ligands
+ ChEBI
+
+
+
+
+
+
+
+
+ CHEBI:52845
+ cyclic organic group
+
+
+
+
+
+
+
+
+ CHEBI:53310
+ co-polymer
+
+
+
+
+
+
+
+
+ CHEBI:53511
+ block copolymer
+
+
+
+
+
+
+
+
+ CHEBI:53512
+ diblock copolymer
+
+
+
+
+
+
+
+
+ CHEBI:53513
+ triblock copolymer
+
+
+
+
+
+
+
+
+ CHEBI:53516
+ statistical copolymer
+
+
+
+
+
+
+
+
+ CHEBI:53517
+ alternating copolymer
+
+
+
+
+
+
+
+
+ CHEBI:53518
+ graft polymer
+
+
+
+
+
+
+
+
+ CHEBI:53519
+ graft copolymer
+
+
+
+
+
+
+
+
+ CHEBI:53520
+ periodic copolymer
+
+
+
+
+
+
+
+
+ CHEBI:53521
+ random copolymer
+
+
+
+
+
+
+
+
+ CHEBI:53522
+ tactic polymer
+
+
+
+
+
+
+
+
+ CHEBI:73474
+ acetylenic compound
+
+
+
+
+
+
+
+
+ The formation of a protein trimer, a macromolecular structure consisting of three noncovalently associated identical or nonidentical subunits.
+ http://purl.obolibrary.org/obo/go/releases/2022-01-13/go.owl
+ GOC:hjd
+ protein trimer assembly
+ protein trimer biosynthesis
+ protein trimer biosynthetic process
+ protein trimer formation
+ biological_process
+ GO:0070206
+ protein trimerization
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a boryl group (-BR'R').
+ MOP:0000000
+ borylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a boryl group (-BR'R').
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a methanidyl group.
+ methanidylation
+ MOP:0000001
+ has_participant: CHEBI:29361
+ methanidylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a methanidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an azaniumyl group.
+ azaniumylation
+ MOP:0000002
+ has_participant: CHEBI:48284
+ azaniumylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an azaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a formyl group.
+ formylation
+ MOP:0000003
+ has_participant: CHEBI:42485
+ formylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a formyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an acetonyl group.
+ acetonylation
+ MOP:0000004
+ has_participant: CHEBI:48056
+ acetonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an acetonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-cystyl group.
+ L-cystylation
+ MOP:0000005
+ has_participant: CHEBI:50057
+ L-cystylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-cystinyl group.
+ L-cystinylation
+ MOP:0000006
+ has_participant: CHEBI:50066
+ L-cystinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-cystinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-cystyl group.
+ D-cystylation
+ MOP:0000007
+ has_participant: CHEBI:50049
+ D-cystylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cystinyl group.
+ cystinylation
+ MOP:0000008
+ has_participant: CHEBI:50050
+ cystinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cystinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cystyl group.
+ cystylation
+ MOP:0000009
+ has_participant: CHEBI:23514
+ cystylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cysteinyl group.
+ cysteinylation
+ MOP:0000010
+ has_participant: CHEBI:23511
+ cysteinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-cysteinyl group.
+ L-cysteinylation
+ MOP:0000011
+ has_participant: CHEBI:32447
+ L-cysteinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-cysteinyl group.
+ D-cysteinylation
+ MOP:0000012
+ has_participant: CHEBI:32452
+ D-cysteinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cystein-S-yl group.
+ cystein-S-ylation
+ MOP:0000013
+ has_participant: CHEBI:32795
+ cystein-S-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-cystein-S-yl group.
+ D-cystein-S-ylation
+ MOP:0000014
+ has_participant: CHEBI:32794
+ D-cystein-S-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-cystein-S-yl group.
+ L-cystein-S-ylation
+ MOP:0000015
+ has_participant: CHEBI:32793
+ L-cystein-S-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a methionyl group.
+ methionylation
+ MOP:0000016
+ has_participant: CHEBI:37902
+ methionylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-methionyl group.
+ L-methionylation
+ MOP:0000017
+ has_participant: CHEBI:49038
+ L-methionylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-formyl-L-methionyl group.
+ N-formyl-L-methionylation
+ MOP:0000018
+ has_participant: CHEBI:49298
+ N-formyl-L-methionylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-formyl-L-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-methionyl group.
+ D-methionylation
+ MOP:0000019
+ has_participant: CHEBI:32640
+ D-methionylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an (R)-lipoyl group.
+ (R)-lipoylation
+ MOP:0000020
+ has_participant: CHEBI:38232
+ (R)-lipoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an (R)-lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an (S)-lipoyl group.
+ (S)-lipoylation
+ MOP:0000021
+ has_participant: CHEBI:38233
+ (S)-lipoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an (S)-lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a lipoyl group.
+ lipoylation
+ MOP:0000022
+ has_participant: CHEBI:25064
+ lipoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an (R)-dihydrolipoyl group.
+ (R)-dihydrolipoylation
+ MOP:0000023
+ has_participant: CHEBI:30319
+ (R)-dihydrolipoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an (R)-dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an (S)-dihydrolipoyl group.
+ (S)-dihydrolipoylation
+ MOP:0000024
+ has_participant: CHEBI:50489
+ (S)-dihydrolipoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an (S)-dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-sialoyl group.
+ alpha-sialoylation
+ MOP:0000025
+ has_participant: CHEBI:32960
+ alpha-sialoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-sialoyl group.
+ beta-sialoylation
+ MOP:0000026
+ has_participant: CHEBI:32961
+ beta-sialoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a glyceroyl group.
+ glyceroylation
+ MOP:0000027
+ has_participant: CHEBI:30750
+ glyceroylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a glyceroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a carboacyl group.
+ carboacylation
+ MOP:0000028
+ carboacylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an univalent carboacyl group.
+ univalent carboacylation
+ MOP:0000029
+ has_participant: CHEBI:27207
+ univalent carboacylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an univalent carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an acetyl group.
+ acetylation
+ MOP:0000030
+ has_participant: CHEBI:40574
+ acetylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an acetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-aminoacyl group.
+ alpha-aminoacylation
+ MOP:0000031
+ has_participant: CHEBI:22487
+ alpha-aminoacylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-aminoacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alanyl group.
+ alanylation
+ MOP:0000032
+ has_participant: CHEBI:22280
+ alanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-alanyl group.
+ L-alanylation
+ MOP:0000033
+ has_participant: CHEBI:32433
+ L-alanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-alanyl group.
+ D-alanylation
+ MOP:0000034
+ has_participant: CHEBI:32437
+ D-alanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-aspartyl group.
+ alpha-aspartylation
+ MOP:0000035
+ has_participant: CHEBI:22445
+ alpha-aspartylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-alpha-aspartyl group.
+ L-alpha-aspartylation
+ MOP:0000036
+ has_participant: CHEBI:32462
+ L-alpha-aspartylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-alpha-aspartyl group.
+ D-alpha-aspartylation
+ MOP:0000037
+ has_participant: CHEBI:32466
+ D-alpha-aspartylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-glutamyl group.
+ alpha-glutamylation
+ MOP:0000038
+ has_participant: CHEBI:22453
+ alpha-glutamylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-alpha-glutamyl group.
+ L-alpha-glutamylation
+ MOP:0000039
+ has_participant: CHEBI:46855
+ L-alpha-glutamylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-alpha-glutamyl group.
+ D-alpha-glutamylation
+ MOP:0000040
+ has_participant: CHEBI:32479
+ D-alpha-glutamylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a pteroylglutamyl group.
+ pteroylglutamylation
+ MOP:0000041
+ has_participant: CHEBI:26380
+ pteroylglutamylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a pteroylglutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a phenylalanyl group.
+ phenylalanylation
+ MOP:0000042
+ has_participant: CHEBI:25987
+ phenylalanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-phenylalanyl group.
+ L-phenylalanylation
+ MOP:0000043
+ has_participant: CHEBI:32496
+ L-phenylalanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-phenylalanyl group.
+ D-phenylalanylation
+ MOP:0000044
+ has_participant: CHEBI:32500
+ D-phenylalanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a glycyl group.
+ glycylation
+ MOP:0000045
+ has_participant: CHEBI:46740
+ glycylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a glycyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a histidyl group.
+ histidylation
+ MOP:0000046
+ has_participant: CHEBI:37906
+ histidylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-histidyl group.
+ L-histidylation
+ MOP:0000047
+ has_participant: CHEBI:32514
+ L-histidylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-histidyl group.
+ D-histidylation
+ MOP:0000048
+ has_participant: CHEBI:32522
+ D-histidylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an isoleucyl group.
+ isoleucylation
+ MOP:0000049
+ has_participant: CHEBI:37905
+ isoleucylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-isoleucyl group.
+ L-isoleucylation
+ MOP:0000050
+ has_participant: CHEBI:32606
+ L-isoleucylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-isoleucyl group.
+ D-isoleucylation
+ MOP:0000051
+ has_participant: CHEBI:32610
+ D-isoleucylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a lysyl group.
+ lysylation
+ MOP:0000052
+ has_participant: CHEBI:37903
+ lysylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-lysyl group.
+ L-lysylation
+ MOP:0000053
+ has_participant: CHEBI:32553
+ L-lysylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a deoxyhypusinyl group.
+ deoxyhypusinylation
+ MOP:0000054
+ has_participant: CHEBI:50039
+ deoxyhypusinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a deoxyhypusinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-lysyl group.
+ D-lysylation
+ MOP:0000055
+ has_participant: CHEBI:32559
+ D-lysylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a leucyl group.
+ leucylation
+ MOP:0000056
+ has_participant: CHEBI:37904
+ leucylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-leucyl group.
+ L-leucylation
+ MOP:0000057
+ has_participant: CHEBI:32621
+ L-leucylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-leucyl group.
+ D-leucylation
+ MOP:0000058
+ has_participant: CHEBI:32625
+ D-leucylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an asparaginyl group.
+ asparaginylation
+ MOP:0000059
+ has_participant: CHEBI:22656
+ asparaginylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-asparaginyl group.
+ L-asparaginylation
+ MOP:0000060
+ has_participant: CHEBI:50348
+ L-asparaginylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-asparaginyl group.
+ D-asparaginylation
+ MOP:0000061
+ has_participant: CHEBI:32653
+ D-asparaginylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a prolyl group.
+ prolylation
+ MOP:0000062
+ has_participant: CHEBI:26274
+ prolylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-prolyl group.
+ L-prolylation
+ MOP:0000063
+ has_participant: CHEBI:32865
+ L-prolylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-prolyl group.
+ D-prolylation
+ MOP:0000064
+ has_participant: CHEBI:32869
+ D-prolylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a glutaminyl group.
+ glutaminylation
+ MOP:0000065
+ has_participant: CHEBI:24320
+ glutaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-glutaminyl group.
+ L-glutaminylation
+ MOP:0000066
+ has_participant: CHEBI:32667
+ L-glutaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-glutaminyl group.
+ D-glutaminylation
+ MOP:0000067
+ has_participant: CHEBI:32674
+ D-glutaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a seryl group.
+ serylation
+ MOP:0000068
+ has_participant: CHEBI:37901
+ serylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-seryl group.
+ L-serylation
+ MOP:0000069
+ has_participant: CHEBI:32838
+ L-serylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-seryl group.
+ D-serylation
+ MOP:0000070
+ has_participant: CHEBI:32842
+ D-serylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a threonyl group.
+ threonylation
+ MOP:0000071
+ has_participant: CHEBI:37900
+ threonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-threonyl group.
+ L-threonylation
+ MOP:0000072
+ has_participant: CHEBI:32823
+ L-threonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-threonyl group.
+ D-threonylation
+ MOP:0000073
+ has_participant: CHEBI:32829
+ D-threonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a selenocysteinyl group.
+ selenocysteinylation
+ MOP:0000074
+ has_participant: CHEBI:32755
+ selenocysteinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-selenocysteinyl group.
+ L-selenocysteinylation
+ MOP:0000075
+ has_participant: CHEBI:32745
+ L-selenocysteinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-selenocysteinyl group.
+ D-selenocysteinylation
+ MOP:0000076
+ has_participant: CHEBI:32749
+ D-selenocysteinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a valyl group.
+ valylation
+ MOP:0000077
+ has_participant: CHEBI:37897
+ valylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-valyl group.
+ L-valylation
+ MOP:0000078
+ has_participant: CHEBI:32853
+ L-valylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-valyl group.
+ D-valylation
+ MOP:0000079
+ has_participant: CHEBI:32857
+ D-valylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tryptophyl group.
+ tryptophylation
+ MOP:0000080
+ has_participant: CHEBI:37899
+ tryptophylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-tryptophyl group.
+ L-tryptophylation
+ MOP:0000081
+ has_participant: CHEBI:32706
+ L-tryptophylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-tryptophyl group.
+ D-tryptophylation
+ MOP:0000082
+ has_participant: CHEBI:32718
+ D-tryptophylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tyrosyl group.
+ tyrosylation
+ MOP:0000083
+ has_participant: CHEBI:37898
+ tyrosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-tyrosyl group.
+ L-tyrosylation
+ MOP:0000084
+ has_participant: CHEBI:32764
+ L-tyrosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-tyrosyl group.
+ D-tyrosylation
+ MOP:0000085
+ has_participant: CHEBI:32778
+ D-tyrosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an arginyl group.
+ arginylation
+ MOP:0000086
+ has_participant: CHEBI:22619
+ arginylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-arginyl group.
+ L-arginylation
+ MOP:0000087
+ has_participant: CHEBI:32684
+ L-arginylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-arginyl group.
+ D-arginylation
+ MOP:0000088
+ has_participant: CHEBI:32691
+ D-arginylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a benzoyl group.
+ benzoylation
+ MOP:0000089
+ has_participant: CHEBI:22733
+ benzoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a benzoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-aspartyl group.
+ beta-aspartylation
+ MOP:0000090
+ has_participant: CHEBI:22832
+ beta-aspartylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-beta-aspartyl group.
+ D-beta-aspartylation
+ MOP:0000091
+ has_participant: CHEBI:32467
+ D-beta-aspartylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-beta-aspartyl group.
+ L-beta-aspartylation
+ MOP:0000092
+ has_participant: CHEBI:48098
+ L-beta-aspartylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a biotinyl group.
+ biotinylation
+ MOP:0000093
+ has_participant: CHEBI:22885
+ biotinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a biotinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a butyryl group.
+ butyrylation
+ MOP:0000094
+ has_participant: CHEBI:22972
+ butyrylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a butyryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a carbamoyl group.
+ carbamoylation
+ MOP:0000095
+ has_participant: CHEBI:23004
+ carbamoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a carbamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a C-aminocarbonohydrazonoyl group.
+ C-aminocarbonohydrazonoylation
+ MOP:0000096
+ has_participant: CHEBI:48223
+ C-aminocarbonohydrazonoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a C-aminocarbonohydrazonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-(aminomethylidene)hydrazinyl group.
+ 2-(aminomethylidene)hydrazinylation
+ MOP:0000097
+ has_participant: CHEBI:48244
+ 2-(aminomethylidene)hydrazinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-(aminomethylidene)hydrazinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a carbamoylcarbamoyl group.
+ carbamoylcarbamoylation
+ MOP:0000098
+ has_participant: CHEBI:48083
+ carbamoylcarbamoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a carbamoylcarbamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a carbamothioyl group.
+ carbamothioylation
+ MOP:0000099
+ has_participant: CHEBI:48225
+ carbamothioylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a carbamothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an acetylazanediyl group.
+ acetylazanediylation
+ MOP:0000100
+ has_participant: CHEBI:48073
+ acetylazanediylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an acetylazanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an oxamoyl group.
+ oxamoylation
+ MOP:0000101
+ has_participant: CHEBI:48246
+ oxamoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an oxamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cholyl group.
+ cholylation
+ MOP:0000102
+ has_participant: CHEBI:23220
+ cholylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cholyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an enoyl group.
+ enoylation
+ MOP:0000103
+ has_participant: CHEBI:23916
+ enoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a fatty-acyl group.
+ fatty-acylation
+ MOP:0000104
+ has_participant: CHEBI:24027
+ fatty-acylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a fatty-acyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an arachidonoyl group.
+ arachidonoylation
+ MOP:0000105
+ has_participant: CHEBI:22610
+ arachidonoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an arachidonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an arachidoyl group.
+ arachidoylation
+ MOP:0000106
+ has_participant: CHEBI:22614
+ arachidoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an arachidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a behenoyl group.
+ behenoylation
+ MOP:0000107
+ has_participant: CHEBI:22696
+ behenoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a behenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cerotoyl group.
+ cerotoylation
+ MOP:0000108
+ has_participant: CHEBI:23080
+ cerotoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cerotoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a decanoyl group.
+ decanoylation
+ MOP:0000109
+ has_participant: CHEBI:23574
+ decanoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a decanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a dodecenoyl group.
+ dodecenoylation
+ MOP:0000110
+ has_participant: CHEBI:23868
+ dodecenoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a dodecenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an eleostearoyl group.
+ eleostearoylation
+ MOP:0000111
+ has_participant: CHEBI:23908
+ eleostearoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an eleostearoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a mycolyl group.
+ mycolylation
+ MOP:0000112
+ has_participant: CHEBI:25439
+ mycolylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a mycolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a nervonoyl group.
+ nervonoylation
+ MOP:0000113
+ has_participant: CHEBI:25503
+ nervonoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a nervonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an octanoyl group.
+ octanoylation
+ MOP:0000114
+ has_participant: CHEBI:25650
+ octanoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an octanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a palmitoleoyl group.
+ palmitoleoylation
+ MOP:0000115
+ has_participant: CHEBI:25837
+ palmitoleoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a palmitoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a palmitoyl group.
+ palmitoylation
+ MOP:0000116
+ has_participant: CHEBI:45021
+ palmitoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a palmitoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a stearoyl group.
+ stearoylation
+ MOP:0000117
+ has_participant: CHEBI:26753
+ stearoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a stearoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an undecanoyl group.
+ undecanoylation
+ MOP:0000118
+ has_participant: CHEBI:27190
+ undecanoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an undecanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a valeryl group.
+ valerylation
+ MOP:0000119
+ has_participant: CHEBI:27265
+ valerylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a valeryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a hexanoyl group.
+ hexanoylation
+ MOP:0000120
+ has_participant: CHEBI:24574
+ hexanoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a hexanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a heptanoyl group.
+ heptanoylation
+ MOP:0000121
+ has_participant: CHEBI:32363
+ heptanoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a heptanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a nonanoyl group.
+ nonanoylation
+ MOP:0000122
+ has_participant: CHEBI:25580
+ nonanoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a nonanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a lauroyl group.
+ lauroylation
+ MOP:0000123
+ has_participant: CHEBI:32359
+ lauroylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a lauroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a myristoyl group.
+ myristoylation
+ MOP:0000124
+ has_participant: CHEBI:25456
+ myristoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a myristoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a docosenoyl group.
+ docosenoylation
+ MOP:0000125
+ has_participant: CHEBI:50479
+ docosenoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a docosenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cetoleoyl group.
+ cetoleoylation
+ MOP:0000126
+ has_participant: CHEBI:32430
+ cetoleoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cetoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an erucoyl group.
+ erucoylation
+ MOP:0000127
+ has_participant: CHEBI:32394
+ erucoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an erucoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an icosenoyl group.
+ icosenoylation
+ MOP:0000128
+ has_participant: CHEBI:50480
+ icosenoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an icosenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a gadelaidoyl group.
+ gadelaidoylation
+ MOP:0000129
+ has_participant: CHEBI:32424
+ gadelaidoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a gadelaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a gadoleoyl group.
+ gadoleoylation
+ MOP:0000130
+ has_participant: CHEBI:32421
+ gadoleoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a gadoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a gondoyl group.
+ gondoylation
+ MOP:0000131
+ has_participant: CHEBI:32427
+ gondoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a gondoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a heptatrienoyl group.
+ heptatrienoylation
+ MOP:0000132
+ has_participant: CHEBI:50486
+ heptatrienoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a heptatrienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a trans,trans-hepta-2,4,6-trienoyl group.
+ trans,trans-hepta-2,4,6-trienoylation
+ MOP:0000133
+ has_participant: CHEBI:30771
+ trans,trans-hepta-2,4,6-trienoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a trans,trans-hepta-2,4,6-trienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an octadecenoyl group.
+ octadecenoylation
+ MOP:0000134
+ has_participant: CHEBI:50499
+ octadecenoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an octadecenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an octadec-6-enoyl group.
+ octadec-6-enoylation
+ MOP:0000135
+ has_participant: CHEBI:50497
+ octadec-6-enoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an octadec-6-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a petroselaidoyl group.
+ petroselaidoylation
+ MOP:0000136
+ has_participant: CHEBI:32378
+ petroselaidoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a petroselaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a petroselinoyl group.
+ petroselinoylation
+ MOP:0000137
+ has_participant: CHEBI:32376
+ petroselinoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a petroselinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a vaccenoyl group.
+ vaccenoylation
+ MOP:0000138
+ has_participant: CHEBI:27261
+ vaccenoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cis-vaccenoyl group.
+ cis-vaccenoylation
+ MOP:0000139
+ has_participant: CHEBI:23313
+ cis-vaccenoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cis-vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a trans-vaccenoyl group.
+ trans-vaccenoylation
+ MOP:0000140
+ has_participant: CHEBI:27080
+ trans-vaccenoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a trans-vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an octadec-9-enoyl group.
+ octadec-9-enoylation
+ MOP:0000141
+ has_participant: CHEBI:50500
+ octadec-9-enoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an octadec-9-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an oleoyl group.
+ oleoylation
+ MOP:0000142
+ has_participant: CHEBI:25667
+ oleoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an oleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an elaidoyl group.
+ elaidoylation
+ MOP:0000143
+ has_participant: CHEBI:23904
+ elaidoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an elaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a margaroyl group.
+ margaroylation
+ MOP:0000144
+ has_participant: CHEBI:32367
+ margaroylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a margaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a melissoyl group.
+ melissoylation
+ MOP:0000145
+ has_participant: CHEBI:31016
+ melissoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a melissoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a myristoleoyl group.
+ myristoleoylation
+ MOP:0000146
+ has_participant: CHEBI:32371
+ myristoleoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a myristoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an obtusiloyl group.
+ obtusiloylation
+ MOP:0000147
+ has_participant: CHEBI:33162
+ obtusiloylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an obtusiloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a lignoceroyl group.
+ lignoceroylation
+ MOP:0000148
+ has_participant: CHEBI:31015
+ lignoceroylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a lignoceroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a linoleoyl group.
+ linoleoylation
+ MOP:0000149
+ has_participant: CHEBI:32386
+ linoleoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a linoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a parinaroyl group.
+ parinaroylation
+ MOP:0000150
+ has_participant: CHEBI:50501
+ parinaroylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cis-parinaroyl group.
+ cis-parinaroylation
+ MOP:0000151
+ has_participant: CHEBI:32415
+ cis-parinaroylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cis-parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a trans-parinaroyl group.
+ trans-parinaroylation
+ MOP:0000152
+ has_participant: CHEBI:32417
+ trans-parinaroylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a trans-parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a gamma-glutamyl group.
+ gamma-glutamylation
+ MOP:0000153
+ has_participant: CHEBI:24190
+ gamma-glutamylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-gamma-glutamyl group.
+ L-gamma-glutamylation
+ MOP:0000154
+ has_participant: CHEBI:32474
+ L-gamma-glutamylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-gamma-glutamyl group.
+ D-gamma-glutamylation
+ MOP:0000155
+ has_participant: CHEBI:32480
+ D-gamma-glutamylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a glucuronosyl group.
+ glucuronosylation
+ MOP:0000156
+ has_participant: CHEBI:24303
+ glucuronosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a glucuronosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-glucuronoyl group.
+ D-glucuronoylation
+ MOP:0000157
+ has_participant: CHEBI:24307
+ D-glucuronoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-glucuronoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a glyceroyl 2,3-dihydroxypropanoyl group.
+ glyceroyl 2,3-dihydroxypropanoylation
+ MOP:0000158
+ has_participant: CHEBI:24363
+ glyceroyl 2,3-dihydroxypropanoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a glyceroyl 2,3-dihydroxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a glyceryl group.
+ glycerylation
+ MOP:0000159
+ has_participant: CHEBI:24364
+ glycerylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a glyceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a glycidoyl 2,3-epoxypropanoyl group.
+ glycidoyl 2,3-epoxypropanoylation
+ MOP:0000160
+ has_participant: CHEBI:24365
+ glycidoyl 2,3-epoxypropanoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a glycidoyl 2,3-epoxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a glycoloyl group.
+ glycoloylation
+ MOP:0000161
+ has_participant: CHEBI:30884
+ glycoloylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a glycoloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a glycosyl group.
+ glycosylation
+ MOP:0000162
+ has_participant: CHEBI:24403
+ glycosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a glycosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a galactosyl group.
+ galactosylation
+ MOP:0000163
+ has_participant: CHEBI:24164
+ galactosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-D-galactosyl group.
+ MOP:0000168
+ beta-D-galactosylation
+ MOP:0000164
+ has_participant: CHEBI:16289
+ beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-L-fucosyl-1,2-beta-D-galactosyl group.
+ alpha-L-fucosyl-1,2-beta-D-galactosylation
+ MOP:0000165
+ has_participant: CHEBI:16124
+ alpha-L-fucosyl-1,2-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-L-fucosyl-1,2-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ alpha-N-acetylneuraminyl-2,3-beta-D-galactosylation
+ MOP:0000166
+ has_participant: CHEBI:16361
+ alpha-N-acetylneuraminyl-2,3-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosylation
+ MOP:0000167
+ has_participant: CHEBI:17483
+ alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a glucosyl group.
+ MOP:0000172
+ glucosylation
+ MOP:0000169
+ has_participant: CHEBI:24281
+ glucosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosyl group.
+ D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosylation
+ MOP:0000170
+ has_participant: CHEBI:17227
+ D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-galactosyl-1,4beta-D-glucosyl group.
+ D-galactosyl-1,4beta-D-glucosylation
+ MOP:0000171
+ has_participant: CHEBI:20966
+ D-galactosyl-1,4beta-D-glucosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-galactosyl-1,4beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-glucosyl group.
+ alpha-glucosylation
+ MOP:0000173
+ has_participant: CHEBI:30684
+ alpha-glucosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-glucosyl group.
+ beta-glucosylation
+ MOP:0000174
+ has_participant: CHEBI:30697
+ beta-glucosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-galactosyl-(1->4)-beta-D-glucosyl group.
+ D-galactosyl-(1->4)-beta-D-glucosylation
+ MOP:0000175
+ has_participant: CHEBI:18018
+ D-galactosyl-(1->4)-beta-D-glucosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-galactosyl-(1->4)-beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a glycosaminyl group.
+ glycosaminylation
+ MOP:0000176
+ has_participant: CHEBI:24399
+ glycosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a glycosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a galactosaminyl group.
+ galactosaminylation
+ MOP:0000177
+ has_participant: CHEBI:24160
+ galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-D-galactosaminyl group.
+ N-acetyl-D-galactosaminylation
+ MOP:0000178
+ has_participant: CHEBI:21507
+ N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminyl group.
+ alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminylation
+ MOP:0000179
+ has_participant: CHEBI:17850
+ alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminylation
+ MOP:0000180
+ has_participant: CHEBI:16565
+ alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminylation
+ MOP:0000181
+ has_participant: CHEBI:16901
+ alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+ MOP:0000182
+ has_participant: CHEBI:15876
+ beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+ MOP:0000183
+ has_participant: CHEBI:17723
+ beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminylation
+ MOP:0000184
+ has_participant: CHEBI:16117
+ beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ beta-D-galactosyl-1,3-N-acetyl-D-galactosaminylation
+ MOP:0000185
+ has_participant: CHEBI:22783
+ beta-D-galactosyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+ MOP:0000186
+ has_participant: CHEBI:17581
+ N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminyl group.
+ N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminylation
+ MOP:0000187
+ has_participant: CHEBI:16250
+ N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminyl group.
+ N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminylation
+ MOP:0000188
+ has_participant: CHEBI:16478
+ N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a glucosaminyl group.
+ glucosaminylation
+ MOP:0000189
+ has_participant: CHEBI:24272
+ glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-D-glucosaminyl group.
+ N-acetyl-D-glucosaminylation
+ MOP:0000190
+ has_participant: CHEBI:21524
+ N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ 1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminylation
+ MOP:0000191
+ has_participant: CHEBI:18914
+ 1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 3-O-beta-D-galactosyl-N-acetyl-D-glucosaminyl group.
+ 3-O-beta-D-galactosyl-N-acetyl-D-glucosaminylation
+ MOP:0000192
+ has_participant: CHEBI:18915
+ 3-O-beta-D-galactosyl-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 3-O-beta-D-galactosyl-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ 1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminylation
+ MOP:0000193
+ has_participant: CHEBI:18939
+ 1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+ MOP:0000194
+ has_participant: CHEBI:17571
+ beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+ MOP:0000195
+ has_participant: CHEBI:17785
+ alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminyl group.
+ alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminylation
+ MOP:0000196
+ has_participant: CHEBI:22381
+ alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminyl group.
+ beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminylation
+ MOP:0000197
+ has_participant: CHEBI:22779
+ beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+ MOP:0000198
+ has_participant: CHEBI:21580
+ N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+ MOP:0000199
+ has_participant: CHEBI:21581
+ N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+ MOP:0000200
+ has_participant: CHEBI:21582
+ N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+ MOP:0000201
+ has_participant: CHEBI:21583
+ N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+ MOP:0000202
+ has_participant: CHEBI:16059
+ N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+ MOP:0000203
+ has_participant: CHEBI:16198
+ N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an iduronosyl group.
+ iduronosylation
+ MOP:0000204
+ has_participant: CHEBI:24770
+ iduronosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an iduronosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-inosinyl group.
+ 5'-inosinylation
+ MOP:0000205
+ has_participant: CHEBI:24845
+ 5'-inosinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-inosinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a mannosyl group.
+ MOP:0000209
+ mannosylation
+ MOP:0000206
+ has_participant: CHEBI:25171
+ mannosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a (N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ (N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosylation
+ MOP:0000207
+ has_participant: CHEBI:18638
+ (N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a (N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-D-mannosyl-1,3-(r1)-beta-D-mannosyl group.
+ alpha-D-mannosyl-1,3-(r1)-beta-D-mannosylation
+ MOP:0000208
+ has_participant: CHEBI:22406
+ alpha-D-mannosyl-1,3-(r1)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-D-mannosyl-1,3-(r1)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-mannosyl group.
+ alpha-mannosylation
+ MOP:0000210
+ has_participant: CHEBI:30689
+ alpha-mannosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosyl group.
+ N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosylation
+ MOP:0000211
+ has_participant: CHEBI:32618
+ N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosyl group.
+ N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosylation
+ MOP:0000212
+ has_participant: CHEBI:32890
+ N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosylation
+ MOP:0000213
+ has_participant: CHEBI:21589
+ N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosyl group.
+ N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosylation
+ MOP:0000214
+ has_participant: CHEBI:32601
+ N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosyl group.
+ N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosylation
+ MOP:0000215
+ has_participant: CHEBI:32602
+ N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-D-mannosyl-(1->3)-beta-D-mannosyl group.
+ alpha-D-mannosyl-(1->3)-beta-D-mannosylation
+ MOP:0000216
+ has_participant: CHEBI:32591
+ alpha-D-mannosyl-(1->3)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-D-mannosyl-(1->3)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a neuraminosyl group.
+ neuraminosylation
+ MOP:0000217
+ has_participant: CHEBI:25509
+ neuraminosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a neuraminosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a neuraminoyl group.
+ neuraminoylation
+ MOP:0000218
+ has_participant: CHEBI:25510
+ neuraminoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a neuraminoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a ribosyl group.
+ MOP:0000221
+ ribosylation
+ MOP:0000219
+ has_participant: CHEBI:26566
+ ribosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a ribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an adenosinediphosphoribosyl group.
+ adenosinediphosphoribosylation
+ MOP:0000220
+ has_participant: CHEBI:22259
+ adenosinediphosphoribosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an adenosinediphosphoribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-deoxyribosyl group.
+ 2-deoxyribosylation
+ MOP:0000222
+ has_participant: CHEBI:30720
+ 2-deoxyribosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-deoxyribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a sialosyl group.
+ sialosylation
+ MOP:0000223
+ has_participant: CHEBI:26668
+ sialosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a sialosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a hemicystyl group.
+ hemicystylation
+ MOP:0000224
+ has_participant: CHEBI:24492
+ hemicystylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a hemicystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a mevalonoyl group.
+ mevalonoylation
+ MOP:0000225
+ has_participant: CHEBI:25353
+ mevalonoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a mevalonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a montanoyl group.
+ montanoylation
+ MOP:0000226
+ has_participant: CHEBI:25417
+ montanoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a montanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a muramyl group.
+ muramylation
+ MOP:0000227
+ has_participant: CHEBI:25433
+ muramylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a nucleotidyl group.
+ nucleotidylation
+ MOP:0000228
+ has_participant: CHEBI:25613
+ nucleotidylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a nucleotidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-adenylyl group.
+ 5'-adenylylation
+ MOP:0000229
+ has_participant: CHEBI:22263
+ 5'-adenylylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-adenylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-cytidylyl group.
+ 5'-cytidylylation
+ MOP:0000230
+ has_participant: CHEBI:23526
+ 5'-cytidylylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-cytidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-thymidylyl group.
+ 5'-thymidylylation
+ MOP:0000231
+ has_participant: CHEBI:27003
+ 5'-thymidylylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-thymidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-uridylyl group.
+ 5'-uridylylation
+ MOP:0000232
+ has_participant: CHEBI:27244
+ 5'-uridylylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-uridylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-guanylyl group.
+ 5'-guanylylation
+ MOP:0000233
+ has_participant: CHEBI:24460
+ 5'-guanylylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-guanylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-ribothymidylyl group.
+ 5'-ribothymidylylation
+ MOP:0000234
+ has_participant: CHEBI:26569
+ 5'-ribothymidylylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-ribothymidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-inosinylyl group.
+ 5'-inosinylylation
+ MOP:0000235
+ has_participant: CHEBI:33512
+ 5'-inosinylylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-inosinylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a pantothenyl group.
+ pantothenylation
+ MOP:0000236
+ has_participant: CHEBI:25850
+ pantothenylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a pantothenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a pantoyl group.
+ pantoylation
+ MOP:0000237
+ has_participant: CHEBI:25851
+ pantoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a pantoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a peptidyl group.
+ peptidylation
+ MOP:0000238
+ has_participant: CHEBI:25907
+ peptidylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a peptidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a phthalyl group.
+ phthalylation
+ MOP:0000239
+ has_participant: CHEBI:26096
+ phthalylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a phthalyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a propionyl group.
+ propionylation
+ MOP:0000240
+ has_participant: CHEBI:26294
+ propionylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a propionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a pyruvoyl group.
+ pyruvoylation
+ MOP:0000241
+ has_participant: CHEBI:45360
+ pyruvoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a pyruvoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a retinoyl group.
+ retinoylation
+ MOP:0000242
+ has_participant: CHEBI:26539
+ retinoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a retinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a sialoyl group.
+ sialoylation
+ MOP:0000243
+ has_participant: CHEBI:26670
+ sialoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 3-carboxypropanoyl group.
+ 3-carboxypropanoylation
+ MOP:0000244
+ has_participant: CHEBI:26810
+ 3-carboxypropanoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 3-carboxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a trienoyl group.
+ trienoylation
+ MOP:0000245
+ has_participant: CHEBI:27107
+ trienoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a trienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an anilinocarbonyl group.
+ anilinocarbonylation
+ MOP:0000246
+ has_participant: CHEBI:30692
+ anilinocarbonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an anilinocarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a pteroyl group.
+ pteroylation
+ MOP:0000247
+ has_participant: CHEBI:26379
+ pteroylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a pteroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 3-carboxyprop-2-enoyl group.
+ 3-carboxyprop-2-enoylation
+ MOP:0000248
+ has_participant: CHEBI:37953
+ 3-carboxyprop-2-enoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a (Z)-3-carboxyprop-2-enoyl group.
+ (Z)-3-carboxyprop-2-enoylation
+ MOP:0000249
+ has_participant: CHEBI:25122
+ (Z)-3-carboxyprop-2-enoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a (Z)-3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a (E)-3-carboxyprop-2-enoyl group.
+ (E)-3-carboxyprop-2-enoylation
+ MOP:0000250
+ has_participant: CHEBI:24126
+ (E)-3-carboxyprop-2-enoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a (E)-3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2,6-dichlorobenzoyl group.
+ 2,6-dichlorobenzoylation
+ MOP:0000251
+ has_participant: CHEBI:48625
+ 2,6-dichlorobenzoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2,6-dichlorobenzoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-muramyl group.
+ alpha-muramylation
+ MOP:0000252
+ has_participant: CHEBI:30701
+ alpha-muramylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-muramyl group.
+ beta-muramylation
+ MOP:0000253
+ has_participant: CHEBI:30702
+ beta-muramylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a beta-muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a dihydrolipoyl group.
+ dihydrolipoylation
+ MOP:0000254
+ has_participant: CHEBI:50488
+ dihydrolipoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a sinapoyl group.
+ sinapoylation
+ MOP:0000255
+ has_participant: CHEBI:50561
+ sinapoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a sinapoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a carboxyacetyl group.
+ carboxyacetylation
+ MOP:0000256
+ has_participant: CHEBI:50650
+ carboxyacetylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a carboxyacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a divalent carboacyl group.
+ divalent carboacylation
+ MOP:0000257
+ has_participant: CHEBI:23855
+ divalent carboacylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a divalent carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an aspartoyl group.
+ aspartoylation
+ MOP:0000258
+ has_participant: CHEBI:22663
+ aspartoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-aspartoyl group.
+ L-aspartoylation
+ MOP:0000259
+ has_participant: CHEBI:32464
+ L-aspartoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-aspartoyl group.
+ D-aspartoylation
+ MOP:0000260
+ has_participant: CHEBI:32468
+ D-aspartoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a citraconoyl group.
+ citraconoylation
+ MOP:0000261
+ has_participant: CHEBI:23315
+ citraconoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a citraconoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a glutamoyl group.
+ glutamoylation
+ MOP:0000262
+ has_participant: CHEBI:24322
+ glutamoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-glutamoyl group.
+ D-glutamoylation
+ MOP:0000263
+ has_participant: CHEBI:32481
+ D-glutamoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-glutamoyl group.
+ L-glutamoylation
+ MOP:0000264
+ has_participant: CHEBI:32475
+ L-glutamoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a maloyl group.
+ maloylation
+ MOP:0000265
+ has_participant: CHEBI:25138
+ maloylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a maloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a phthaloyl group.
+ phthaloylation
+ MOP:0000266
+ has_participant: CHEBI:26095
+ phthaloylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a phthaloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a succinyl group.
+ succinylation
+ MOP:0000267
+ has_participant: CHEBI:37952
+ succinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a succinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a butenedioyl group.
+ butenedioylation
+ MOP:0000268
+ has_participant: CHEBI:37954
+ butenedioylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a butenedioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a fumaroyl group.
+ fumaroylation
+ MOP:0000269
+ has_participant: CHEBI:24125
+ fumaroylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a fumaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a maleoyl group.
+ maleoylation
+ MOP:0000270
+ has_participant: CHEBI:25121
+ maleoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a maleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a hexanedioyl group.
+ hexanedioylation
+ MOP:0000271
+ has_participant: CHEBI:48082
+ hexanedioylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a hexanedioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a malonyl group.
+ malonylation
+ MOP:0000272
+ has_participant: CHEBI:25134
+ malonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a malonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an ornithyl group.
+ ornithylation
+ MOP:0000273
+ has_participant: CHEBI:46929
+ ornithylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an ornithyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-ornithyl group.
+ L-ornithylation
+ MOP:0000274
+ has_participant: CHEBI:44700
+ L-ornithylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-ornithyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a half-cystyl group.
+ half-cystylation
+ MOP:0000275
+ has_participant: CHEBI:30770
+ half-cystylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a half-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-tyrosin-O(4)-yl group.
+ L-tyrosin-O(4)-ylation
+ MOP:0000276
+ has_participant: CHEBI:32768
+ L-tyrosin-O(4)-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-threonin-O(3)-yl group.
+ L-threonin-O(3)-ylation
+ MOP:0000277
+ has_participant: CHEBI:32825
+ L-threonin-O(3)-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an L-threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-tyrosin-O(4)-yl group.
+ D-tyrosin-O(4)-ylation
+ MOP:0000278
+ has_participant: CHEBI:32780
+ D-tyrosin-O(4)-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-threonin-O(3)-yl group.
+ D-threonin-O(3)-ylation
+ MOP:0000279
+ has_participant: CHEBI:32831
+ D-threonin-O(3)-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a D-threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tyrosin-O(4)-yl group.
+ tyrosin-O(4)-ylation
+ MOP:0000280
+ has_participant: CHEBI:32788
+ tyrosin-O(4)-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a threonin-O(3)-yl group.
+ threonin-O(3)-ylation
+ MOP:0000281
+ has_participant: CHEBI:26985
+ threonin-O(3)-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an oxalyl group.
+ oxalylation
+ MOP:0000282
+ has_participant: CHEBI:30870
+ oxalylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an oxalyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a fumagillin-2-yl group.
+ fumagillin-2-ylation
+ MOP:0000283
+ has_participant: CHEBI:42601
+ fumagillin-2-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a fumagillin-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an acetoacetyl group.
+ acetoacetylation
+ MOP:0000284
+ has_participant: CHEBI:48051
+ acetoacetylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an acetoacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-linolenoyl group.
+ alpha-linolenoylation
+ MOP:0000285
+ has_participant: CHEBI:32388
+ alpha-linolenoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alpha-linolenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a gamma-linolenoyl group.
+ gamma-linolenoylation
+ MOP:0000286
+ has_participant: CHEBI:32390
+ gamma-linolenoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a gamma-linolenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a carbamimidoyl group.
+ carbamimidoylation
+ MOP:0000287
+ has_participant: CHEBI:48090
+ carbamimidoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a carbamimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a formimidoyl group.
+ formimidoylation
+ MOP:0000288
+ has_participant: CHEBI:24084
+ formimidoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a formimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a trifluoroacetyl group.
+ trifluoroacetylation
+ MOP:0000289
+ has_participant: CHEBI:45888
+ trifluoroacetylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a trifluoroacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a carboxymethyl group.
+ carboxymethylation
+ MOP:0000290
+ has_participant: CHEBI:41402
+ carboxymethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a carboxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a methylenecarbonyl group.
+ methylenecarbonylation
+ MOP:0000291
+ has_participant: CHEBI:43923
+ methylenecarbonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a methylenecarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-hydroxyacetimidoyl group.
+ N-hydroxyacetimidoylation
+ MOP:0000292
+ has_participant: CHEBI:48055
+ N-hydroxyacetimidoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-hydroxyacetimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an acryloyl group.
+ acryloylation
+ MOP:0000293
+ has_participant: CHEBI:48077
+ acryloylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an acryloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tert-butoxycarbonyl group.
+ tert-butoxycarbonylation
+ MOP:0000294
+ has_participant: CHEBI:48502
+ tert-butoxycarbonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tert-butoxycarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfanediyl group.
+ sulfanediylation
+ MOP:0000295
+ has_participant: CHEBI:29830
+ sulfanediylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a phenylsulfanyl group.
+ phenylsulfanylation
+ MOP:0000296
+ has_participant: CHEBI:48499
+ phenylsulfanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a phenylsulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a methylsulfanyl group.
+ methylsulfanylation
+ MOP:0000297
+ has_participant: CHEBI:48563
+ methylsulfanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a methylsulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfaniumyl group.
+ sulfaniumylation
+ MOP:0000298
+ has_participant: CHEBI:36945
+ sulfaniumylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a disulfanidyl group.
+ disulfanidylation
+ MOP:0000299
+ has_participant: CHEBI:29838
+ disulfanidylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a disulfanidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a disulfanediyl group.
+ disulfanediylation
+ MOP:0000300
+ has_participant: CHEBI:29826
+ disulfanediylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a disulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a disulfanyl group.
+ disulfanylation
+ MOP:0000301
+ has_participant: CHEBI:30605
+ disulfanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a disulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tetrasulfanyl group.
+ tetrasulfanylation
+ MOP:0000302
+ has_participant: CHEBI:30607
+ tetrasulfanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tetrasulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tetrasulfanediyl group.
+ tetrasulfanediylation
+ MOP:0000303
+ has_participant: CHEBI:29836
+ tetrasulfanediylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tetrasulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a trisulfanyl group.
+ trisulfanylation
+ MOP:0000304
+ has_participant: CHEBI:30606
+ trisulfanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a trisulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a trisulfanediyl group.
+ trisulfanediylation
+ MOP:0000305
+ has_participant: CHEBI:29834
+ trisulfanediylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a trisulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a pentasulfanyl group.
+ pentasulfanylation
+ MOP:0000306
+ has_participant: CHEBI:30608
+ pentasulfanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a pentasulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a diselanyl group.
+ diselanylation
+ MOP:0000307
+ has_participant: CHEBI:30602
+ diselanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a diselanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tellanyl group.
+ tellanylation
+ MOP:0000308
+ has_participant: CHEBI:30458
+ tellanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tellanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tellanediyl group.
+ tellanediylation
+ MOP:0000309
+ has_participant: CHEBI:30455
+ tellanediylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tellanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tellaniumyl group.
+ tellaniumylation
+ MOP:0000310
+ has_participant: CHEBI:30447
+ tellaniumylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tellaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a ditellanyl group.
+ ditellanylation
+ MOP:0000311
+ has_participant: CHEBI:30601
+ ditellanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a ditellanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an amidyl group.
+ amidylation
+ MOP:0000312
+ has_participant: CHEBI:48373
+ amidylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an amidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an azanediyl group.
+ azanediylation
+ MOP:0000313
+ has_participant: CHEBI:29343
+ azanediylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an azanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-aminoethyl group.
+ 2-aminoethylation
+ MOP:0000314
+ has_participant: CHEBI:22502
+ 2-aminoethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-aminoethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 4-aminobutyl group.
+ 4-aminobutylation
+ MOP:0000315
+ has_participant: CHEBI:50339
+ 4-aminobutylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 4-aminobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an azanetriyl group.
+ azanetriylation
+ MOP:0000316
+ has_participant: CHEBI:30228
+ azanetriylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an azanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a hydrazine-1,2-diyl group.
+ hydrazine-1,2-diylation
+ MOP:0000317
+ has_participant: CHEBI:30098
+ hydrazine-1,2-diylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a hydrazine-1,2-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a diazyn-1-ium-1-yl group.
+ diazyn-1-ium-1-ylation
+ MOP:0000318
+ has_participant: CHEBI:30108
+ diazyn-1-ium-1-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a diazyn-1-ium-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a phosphanetriyl group.
+ phosphanetriylation
+ MOP:0000319
+ has_participant: CHEBI:30206
+ phosphanetriylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a phosphanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a phosphanediyl group.
+ phosphanediylation
+ MOP:0000320
+ has_participant: CHEBI:29944
+ phosphanediylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a phosphanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a phosphanyl group.
+ phosphanylation
+ MOP:0000321
+ has_participant: CHEBI:29936
+ phosphanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a phosphanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a lambda(5)-phosphanyl group.
+ lambda(5)-phosphanylation
+ MOP:0000322
+ has_participant: CHEBI:30284
+ lambda(5)-phosphanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a lambda(5)-phosphanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a phosphaniumyl group.
+ phosphaniumylation
+ MOP:0000323
+ has_participant: CHEBI:30279
+ phosphaniumylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a phosphaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an arsanyl group.
+ arsanylation
+ MOP:0000324
+ has_participant: CHEBI:29759
+ arsanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an arsanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an arsanediyl group.
+ arsanediylation
+ MOP:0000325
+ has_participant: CHEBI:29763
+ arsanediylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an arsanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an arsanetriyl group.
+ arsanetriylation
+ MOP:0000326
+ has_participant: CHEBI:29766
+ arsanetriylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an arsanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an arsaniumyl group.
+ arsaniumylation
+ MOP:0000327
+ has_participant: CHEBI:29842
+ arsaniumylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an arsaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a lambda(5)-arsanyl group.
+ lambda(5)-arsanylation
+ MOP:0000328
+ has_participant: CHEBI:30273
+ lambda(5)-arsanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a lambda(5)-arsanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a stibaniumyl group.
+ stibaniumylation
+ MOP:0000329
+ has_participant: CHEBI:30291
+ stibaniumylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a stibaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a lambda(5)-stibanyl group.
+ lambda(5)-stibanylation
+ MOP:0000330
+ has_participant: CHEBI:30293
+ lambda(5)-stibanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a lambda(5)-stibanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a boranyl group.
+ boranylation
+ MOP:0000331
+ has_participant: CHEBI:33604
+ boranylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a boranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a boranetriyl group.
+ boranetriylation
+ MOP:0000332
+ has_participant: CHEBI:30169
+ boranetriylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a boranetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a boranediyl group.
+ boranediylation
+ MOP:0000333
+ has_participant: CHEBI:38988
+ boranediylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a boranediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a boranuidyl group.
+ boranuidylation
+ MOP:0000334
+ has_participant: CHEBI:30159
+ boranuidylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a boranuidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a germyl group.
+ germylation
+ MOP:0000335
+ has_participant: CHEBI:30542
+ germylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a germyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a germanediyl group.
+ germanediylation
+ MOP:0000336
+ has_participant: CHEBI:30554
+ germanediylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a germanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a germanetetrayl group.
+ germanetetraylation
+ MOP:0000337
+ has_participant: CHEBI:30547
+ germanetetraylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a germanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a germanetriyl group.
+ germanetriylation
+ MOP:0000338
+ has_participant: CHEBI:30544
+ germanetriylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a germanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an silyl group.
+ silylation
+ MOP:0000339
+ has_participant: CHEBI:33478
+ silylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an silyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a silanediyl group.
+ silanediylation
+ MOP:0000340
+ has_participant: CHEBI:30587
+ silanediylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a silanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a silanetriyl group.
+ silanetriylation
+ MOP:0000341
+ has_participant: CHEBI:30576
+ silanetriylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a silanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a silanetetrayl group.
+ silanetetraylation
+ MOP:0000342
+ has_participant: CHEBI:30583
+ silanetetraylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a silanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a disilanyl group.
+ disilanylation
+ MOP:0000343
+ has_participant: CHEBI:30594
+ disilanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a disilanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alumanyl group.
+ alumanylation
+ MOP:0000344
+ has_participant: CHEBI:30135
+ alumanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alumanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a stannyl group.
+ stannylation
+ MOP:0000345
+ has_participant: CHEBI:30540
+ stannylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a stannyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a stannanetriyl group.
+ stannanetriylation
+ MOP:0000346
+ has_participant: CHEBI:30575
+ stannanetriylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a stannanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a plumbanetriyl group.
+ plumbanetriylation
+ MOP:0000347
+ has_participant: CHEBI:30577
+ plumbanetriylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a plumbanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a plumbyl group.
+ plumbylation
+ MOP:0000348
+ has_participant: CHEBI:30543
+ plumbylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a plumbyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a gallanyl group.
+ gallanylation
+ MOP:0000349
+ has_participant: CHEBI:37119
+ gallanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a gallanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an indiganyl group.
+ indiganylation
+ MOP:0000350
+ has_participant: CHEBI:30431
+ indiganylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an indiganyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a thallanyl group.
+ thallanylation
+ MOP:0000351
+ has_participant: CHEBI:30442
+ thallanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a thallanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a phosphatidyl group.
+ phosphatidylation
+ MOP:0000352
+ has_participant: CHEBI:26025
+ phosphatidylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a phosphatidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a nucleosidyl group.
+ nucleosidylation
+ MOP:0000353
+ has_participant: CHEBI:33494
+ nucleosidylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a nucleosidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a guanosyl group.
+ guanosylation
+ MOP:0000354
+ has_participant: CHEBI:24459
+ guanosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a guanosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an inosyl group.
+ inosylation
+ MOP:0000355
+ has_participant: CHEBI:24849
+ inosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an inosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a thymidyl group.
+ thymidylation
+ MOP:0000356
+ has_participant: CHEBI:27002
+ thymidylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a thymidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an adenosyl group.
+ adenosylation
+ MOP:0000357
+ has_participant: CHEBI:33505
+ adenosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an adenosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-adenosyl group.
+ 5'-adenosylation
+ MOP:0000358
+ has_participant: CHEBI:22261
+ 5'-adenosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 5'-adenosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an uridyl group.
+ uridylation
+ MOP:0000359
+ has_participant: CHEBI:27243
+ uridylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an uridyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cytidyl group.
+ cytidylation
+ MOP:0000360
+ has_participant: CHEBI:23525
+ cytidylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cytidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a dolichyl group.
+ dolichylation
+ MOP:0000361
+ has_participant: CHEBI:23883
+ dolichylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a dolichyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-trans,6-trans-farnesyl group.
+ 2-trans,6-trans-farnesylation
+ MOP:0000362
+ has_participant: CHEBI:36535
+ 2-trans,6-trans-farnesylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-trans,6-trans-farnesyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a margaryl group.
+ margarylation
+ MOP:0000363
+ has_participant: CHEBI:32925
+ margarylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a margaryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a methyl group.
+ methylation
+ MOP:0000364
+ has_participant: CHEBI:32875
+ methylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a methyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a methanetetrayl group.
+ methanetetraylation
+ MOP:0000365
+ has_participant: CHEBI:30039
+ methanetetraylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a methanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a methanetriyl group.
+ methanetriylation
+ MOP:0000366
+ has_participant: CHEBI:29433
+ methanetriylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a methanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a trichloromethyl group.
+ trichloromethylation
+ MOP:0000367
+ has_participant: CHEBI:30736
+ trichloromethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a trichloromethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a trifluoromethyl group.
+ trifluoromethylation
+ MOP:0000368
+ has_participant: CHEBI:50127
+ trifluoromethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a trifluoromethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alkyl group.
+ alkylation
+ MOP:0000369
+ has_participant: CHEBI:22323
+ alkylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a butyl group.
+ butylation
+ MOP:0000370
+ has_participant: CHEBI:41264
+ butylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a ceryl group.
+ cerylation
+ MOP:0000371
+ has_participant: CHEBI:23081
+ cerylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a ceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a decyl group.
+ decylation
+ MOP:0000372
+ has_participant: CHEBI:23580
+ decylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a decyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a dodecyl group.
+ dodecylation
+ MOP:0000373
+ has_participant: CHEBI:23870
+ dodecylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a dodecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a heptyl group.
+ heptylation
+ MOP:0000374
+ has_participant: CHEBI:24526
+ heptylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a heptyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a hexyl group.
+ hexylation
+ MOP:0000375
+ has_participant: CHEBI:24593
+ hexylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a hexyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a myricyl group.
+ myricylation
+ MOP:0000376
+ has_participant: CHEBI:25453
+ myricylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a myricyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a myristyl group.
+ myristylation
+ MOP:0000377
+ has_participant: CHEBI:25457
+ myristylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a myristyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a nonyl group.
+ nonylation
+ MOP:0000378
+ has_participant: CHEBI:25589
+ nonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a nonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an octyl group.
+ octylation
+ MOP:0000379
+ has_participant: CHEBI:25657
+ octylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an octyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a palmityl group.
+ palmitylation
+ MOP:0000380
+ has_participant: CHEBI:25842
+ palmitylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a palmityl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a pentyl group.
+ pentylation
+ MOP:0000381
+ has_participant: CHEBI:25902
+ pentylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a pentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a propyl group.
+ propylation
+ MOP:0000382
+ has_participant: CHEBI:26308
+ propylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a propyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a stearyl group.
+ stearylation
+ MOP:0000383
+ has_participant: CHEBI:26755
+ stearylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a stearyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an isopropyl group.
+ isopropylation
+ MOP:0000384
+ has_participant: CHEBI:30353
+ isopropylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an isopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an ethyl group.
+ ethylation
+ MOP:0000385
+ has_participant: CHEBI:37807
+ ethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an ethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an isobutyl group.
+ isobutylation
+ MOP:0000386
+ has_participant: CHEBI:30356
+ isobutylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an isobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a pentan-2-yl group.
+ pentan-2-ylation
+ MOP:0000387
+ has_participant: CHEBI:32880
+ pentan-2-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a pentan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an isopentyl group.
+ isopentylation
+ MOP:0000388
+ has_participant: CHEBI:30359
+ isopentylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an isopentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 3-methylbutan-2-yl group.
+ 3-methylbutan-2-ylation
+ MOP:0000389
+ has_participant: CHEBI:32882
+ 3-methylbutan-2-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 3-methylbutan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tert-pentyl group.
+ tert-pentylation
+ MOP:0000390
+ has_participant: CHEBI:30360
+ tert-pentylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tert-pentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a neopentyl group.
+ neopentylation
+ MOP:0000391
+ has_participant: CHEBI:30357
+ neopentylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a neopentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an undecyl group.
+ undecylation
+ MOP:0000392
+ has_participant: CHEBI:32900
+ undecylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an undecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tridecyl group.
+ tridecylation
+ MOP:0000393
+ has_participant: CHEBI:32908
+ tridecylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tridecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a pentadecyl group.
+ pentadecylation
+ MOP:0000394
+ has_participant: CHEBI:32909
+ pentadecylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a pentadecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a nonadecyl group.
+ nonadecylation
+ MOP:0000395
+ has_participant: CHEBI:32928
+ nonadecylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a nonadecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an arachidyl group.
+ arachidylation
+ MOP:0000396
+ has_participant: CHEBI:32930
+ arachidylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an arachidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a henicosyl group.
+ henicosylation
+ MOP:0000397
+ has_participant: CHEBI:32932
+ henicosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a henicosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a behenyl group.
+ behenylation
+ MOP:0000398
+ has_participant: CHEBI:32933
+ behenylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a behenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tricosyl group.
+ tricosylation
+ MOP:0000399
+ has_participant: CHEBI:32935
+ tricosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tricosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a lignoceryl group.
+ lignocerylation
+ MOP:0000400
+ has_participant: CHEBI:32937
+ lignocerylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a lignoceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a pentacosyl group.
+ pentacosylation
+ MOP:0000401
+ has_participant: CHEBI:32939
+ pentacosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a pentacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a heptacosyl group.
+ heptacosylation
+ MOP:0000402
+ has_participant: CHEBI:32942
+ heptacosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a heptacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a montanyl group.
+ montanylation
+ MOP:0000403
+ has_participant: CHEBI:32944
+ montanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a montanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a nonacosyl group.
+ nonacosylation
+ MOP:0000404
+ has_participant: CHEBI:32945
+ nonacosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a nonacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a sec-butyl group.
+ sec-butylation
+ MOP:0000405
+ has_participant: CHEBI:45557
+ sec-butylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a sec-butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tert-butyl group.
+ tert-butylation
+ MOP:0000406
+ has_participant: CHEBI:30355
+ tert-butylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tert-butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a pentan-3-yl group.
+ pentan-3-ylation
+ MOP:0000407
+ has_participant: CHEBI:32881
+ pentan-3-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a pentan-3-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-chloroethyl group.
+ 2-chloroethylation
+ MOP:0000408
+ has_participant: CHEBI:47553
+ 2-chloroethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-chloroethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 1-chloroethyl group.
+ 1-chloroethylation
+ MOP:0000409
+ has_participant: CHEBI:48099
+ 1-chloroethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 1-chloroethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a hydrocarbyl group.
+ hydrocarbylation
+ MOP:0000410
+ has_participant: CHEBI:33248
+ hydrocarbylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a hydrocarbyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an aryl group.
+ arylation
+ MOP:0000411
+ has_participant: CHEBI:33338
+ arylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an aryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a phenyl group.
+ phenylation
+ MOP:0000412
+ has_participant: CHEBI:30396
+ phenylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a phenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a biphenyl-4-yl group.
+ biphenyl-4-ylation
+ MOP:0000413
+ has_participant: CHEBI:35447
+ biphenyl-4-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a biphenyl-4-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a naphthyl group.
+ naphthylation
+ MOP:0000414
+ has_participant: CHEBI:51140
+ naphthylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 1-naphthyl group.
+ 1-naphthylation
+ MOP:0000415
+ has_participant: CHEBI:51138
+ 1-naphthylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 1-naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-naphthyl group.
+ 2-naphthylation
+ MOP:0000416
+ has_participant: CHEBI:51139
+ 2-naphthylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cycloalkyl group.
+ cycloalkylation
+ MOP:0000417
+ has_participant: CHEBI:33441
+ cycloalkylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cycloalkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cyclobutyl group.
+ cyclobutylation
+ MOP:0000418
+ has_participant: CHEBI:30376
+ cyclobutylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cyclobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cyclopropyl group.
+ cyclopropylation
+ MOP:0000419
+ has_participant: CHEBI:30364
+ cyclopropylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cyclopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alkenyl group.
+ alkenylation
+ MOP:0000420
+ has_participant: CHEBI:37614
+ alkenylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alkenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an oleyl group.
+ oleylation
+ MOP:0000421
+ has_participant: CHEBI:25670
+ oleylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an oleyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an allyl group.
+ allylation
+ MOP:0000422
+ has_participant: CHEBI:30361
+ allylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an allyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an isopropenyl group.
+ isopropenylation
+ MOP:0000423
+ has_participant: CHEBI:30354
+ isopropenylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an isopropenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a vinyl group.
+ vinylation
+ MOP:0000424
+ has_participant: CHEBI:37603
+ vinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a vinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a prenyl group.
+ MOP:0000427
+ prenylation
+ MOP:0000425
+ has_participant: CHEBI:26248
+ prenylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a prenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a phytyl group.
+ phytylation
+ MOP:0000426
+ has_participant: CHEBI:26126
+ phytylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a phytyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a polyprenyl group.
+ polyprenylation
+ MOP:0000428
+ has_participant: CHEBI:26201
+ polyprenylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a polyprenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a farnesyl group.
+ farnesylation
+ MOP:0000429
+ has_participant: CHEBI:24017
+ farnesylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a farnesyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a geranyl group.
+ geranylation
+ MOP:0000430
+ has_participant: CHEBI:24224
+ geranylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a geranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a geranylgeranyl group.
+ geranylgeranylation
+ MOP:0000431
+ has_participant: CHEBI:24231
+ geranylgeranylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a geranylgeranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a retinyl group.
+ retinylation
+ MOP:0000432
+ has_participant: CHEBI:26541
+ retinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a retinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an adamantan-2-yl group.
+ adamantan-2-ylation
+ MOP:0000433
+ has_participant: CHEBI:48078
+ adamantan-2-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an adamantan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cycloalkenyl group.
+ cycloalkenylation
+ MOP:0000434
+ has_participant: CHEBI:48886
+ cycloalkenylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cycloalkenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a campholenic cyclohexenyl group.
+ campholenic cyclohexenylation
+ MOP:0000435
+ has_participant: CHEBI:48885
+ campholenic cyclohexenylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a campholenic cyclohexenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cyclopentadienyl group.
+ cyclopentadienylation
+ MOP:0000436
+ has_participant: CHEBI:30663
+ cyclopentadienylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an eta(5)-cyclopentadienyl group.
+ eta(5)-cyclopentadienylation
+ MOP:0000437
+ has_participant: CHEBI:36763
+ eta(5)-cyclopentadienylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an eta(5)-cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an eta(1)-cyclopentadienyl group.
+ eta(1)-cyclopentadienylation
+ MOP:0000438
+ has_participant: CHEBI:36764
+ eta(1)-cyclopentadienylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an eta(1)-cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an ethene-1,2-diyl group.
+ ethene-1,2-diylation
+ MOP:0000439
+ has_participant: CHEBI:46880
+ ethene-1,2-diylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an ethene-1,2-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an arachidonyl group.
+ arachidonylation
+ MOP:0000440
+ has_participant: CHEBI:22612
+ arachidonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an arachidonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a benzyl group.
+ benzylation
+ MOP:0000441
+ has_participant: CHEBI:22744
+ benzylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a benzyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an anthracen-1-yl group.
+ anthracen-1-ylation
+ MOP:0000442
+ has_participant: CHEBI:48287
+ anthracen-1-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an anthracen-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an anthracen-2-yl group.
+ anthracen-2-ylation
+ MOP:0000443
+ has_participant: CHEBI:48371
+ anthracen-2-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an anthracen-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an imidazolyl group.
+ imidazolylation
+ MOP:0000444
+ has_participant: CHEBI:50052
+ imidazolylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an imidazolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an imidazol-1-yl group.
+ imidazol-1-ylation
+ MOP:0000445
+ has_participant: CHEBI:50053
+ imidazol-1-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an imidazol-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an imidazol-2-yl group.
+ imidazol-2-ylation
+ MOP:0000446
+ has_participant: CHEBI:50054
+ imidazol-2-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an imidazol-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an imidazol-5-yl group.
+ imidazol-5-ylation
+ MOP:0000447
+ has_participant: CHEBI:50055
+ imidazol-5-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an imidazol-5-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an imidazol-4-yl group.
+ imidazol-4-ylation
+ MOP:0000448
+ has_participant: CHEBI:50056
+ imidazol-4-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an imidazol-4-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a furyl group.
+ furylation
+ MOP:0000449
+ has_participant: CHEBI:24131
+ furylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-furyl group.
+ 2-furylation
+ MOP:0000450
+ has_participant: CHEBI:19586
+ 2-furylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 3-furyl group.
+ 3-furylation
+ MOP:0000451
+ has_participant: CHEBI:20025
+ 3-furylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 3-furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a thienyl group.
+ thienylation
+ MOP:0000452
+ has_participant: CHEBI:37991
+ thienylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-thienyl group.
+ 2-thienylation
+ MOP:0000453
+ has_participant: CHEBI:35849
+ 2-thienylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 3-thienyl group.
+ 3-thienylation
+ MOP:0000454
+ has_participant: CHEBI:37992
+ 3-thienylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 3-thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an adenin-9-yl group.
+ adenin-9-ylation
+ MOP:0000455
+ has_participant: CHEBI:30756
+ adenin-9-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an adenin-9-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a guanin-9-yl group.
+ guanin-9-ylation
+ MOP:0000456
+ has_participant: CHEBI:30755
+ guanin-9-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a guanin-9-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an acetimidoyl group.
+ acetimidoylation
+ MOP:0000457
+ has_participant: CHEBI:48050
+ acetimidoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an acetimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an organyl group.
+ organylation
+ MOP:0000458
+ has_participant: CHEBI:33249
+ organylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an organyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an organic heterocyclyl group.
+ organic heterocyclylation
+ MOP:0000459
+ has_participant: CHEBI:33453
+ organic heterocyclylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an organic heterocyclyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a heteroaryl group.
+ heteroarylation
+ MOP:0000460
+ has_participant: CHEBI:33470
+ heteroarylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a heteroaryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 4,4'-dimethoxytriphenylmethyl group.
+ 4,4'-dimethoxytriphenylmethylation
+ MOP:0000461
+ has_participant: CHEBI:51095
+ 4,4'-dimethoxytriphenylmethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 4,4'-dimethoxytriphenylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tauryl group.
+ taurylation
+ MOP:0000462
+ has_participant: CHEBI:26861
+ taurylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tauryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a triflyl group.
+ triflylation
+ MOP:0000463
+ has_participant: CHEBI:48548
+ triflylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a triflyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a glycidyl group.
+ glycidylation
+ MOP:0000464
+ has_participant: CHEBI:24366
+ glycidylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a glycidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfanylmethyl group.
+ sulfanylmethylation
+ MOP:0000465
+ has_participant: CHEBI:50326
+ sulfanylmethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfanylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a selanylmethyl group.
+ selanylmethylation
+ MOP:0000466
+ has_participant: CHEBI:50327
+ selanylmethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a selanylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-carboxyethyl group.
+ 2-carboxyethylation
+ MOP:0000467
+ has_participant: CHEBI:50329
+ 2-carboxyethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-carboxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-amino-2-oxoethyl group.
+ 2-amino-2-oxoethylation
+ MOP:0000468
+ has_participant: CHEBI:50330
+ 2-amino-2-oxoethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-amino-2-oxoethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 3-amino-3-oxopropyl group.
+ 3-amino-3-oxopropylation
+ MOP:0000469
+ has_participant: CHEBI:50331
+ 3-amino-3-oxopropylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 3-amino-3-oxopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-(methylsulfanyl)ethyl group.
+ 2-(methylsulfanyl)ethylation
+ MOP:0000470
+ has_participant: CHEBI:50332
+ 2-(methylsulfanyl)ethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-(methylsulfanyl)ethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 4-hydroxybenzyl group.
+ 4-hydroxybenzylation
+ MOP:0000471
+ has_participant: CHEBI:50336
+ 4-hydroxybenzylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 4-hydroxybenzyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 1H-indol-3-ylmethyl group.
+ 1H-indol-3-ylmethylation
+ MOP:0000472
+ has_participant: CHEBI:50337
+ 1H-indol-3-ylmethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 1H-indol-3-ylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 1H-imidazol-4-ylmethyl group.
+ 1H-imidazol-4-ylmethylation
+ MOP:0000473
+ has_participant: CHEBI:50338
+ 1H-imidazol-4-ylmethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 1H-imidazol-4-ylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 3-carbamimidamidopropyl group.
+ 3-carbamimidamidopropylation
+ MOP:0000474
+ has_participant: CHEBI:50340
+ 3-carbamimidamidopropylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 3-carbamimidamidopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a hydroxymethyl group.
+ hydroxymethylation
+ MOP:0000475
+ has_participant: CHEBI:24712
+ hydroxymethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a hydroxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 1-hydroxyethyl group.
+ 1-hydroxyethylation
+ MOP:0000476
+ has_participant: CHEBI:50341
+ 1-hydroxyethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 1-hydroxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a haloalkyl group.
+ haloalkylation
+ MOP:0000477
+ has_participant: CHEBI:50491
+ haloalkylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a haloalkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-(trimethylsilyl)ethoxymethyl group.
+ 2-(trimethylsilyl)ethoxymethylation
+ MOP:0000478
+ has_participant: CHEBI:51093
+ 2-(trimethylsilyl)ethoxymethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-(trimethylsilyl)ethoxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an acyl group.
+ acylation
+ MOP:0000479
+ you probably want "carboacylation", MOP:0000028, here
+ acylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an acyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an organoheteryl group.
+ organoheterylation
+ MOP:0000480
+ has_participant: CHEBI:33456
+ organoheterylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an organoheteryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an oxalosulfanyl group.
+ oxalosulfanylation
+ MOP:0000481
+ has_participant: CHEBI:30874
+ oxalosulfanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an oxalosulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an organosilyl group.
+ organosilylation
+ MOP:0000482
+ has_participant: CHEBI:33478
+ organosilylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an organosilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a trimethylsilyl group.
+ trimethylsilylation
+ MOP:0000483
+ has_participant: CHEBI:51088
+ trimethylsilylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a trimethylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a triisopropylsilyl group.
+ triisopropylsilylation
+ MOP:0000484
+ has_participant: CHEBI:51089
+ triisopropylsilylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a triisopropylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tert-butyldiphenylsilyl group.
+ tert-butyldiphenylsilylation
+ MOP:0000485
+ has_participant: CHEBI:51090
+ tert-butyldiphenylsilylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tert-butyldiphenylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tert-butyldimethylsilyl group.
+ tert-butyldimethylsilylation
+ MOP:0000486
+ has_participant: CHEBI:51091
+ tert-butyldimethylsilylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tert-butyldimethylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a thioacyl group.
+ thioacylation
+ MOP:0000487
+ has_participant: CHEBI:49063
+ thioacylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a thioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a carbothioacyl group.
+ carbothioacylation
+ MOP:0000488
+ has_participant: CHEBI:49066
+ carbothioacylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an univalent carbothioacyl group.
+ univalent carbothioacylation
+ MOP:0000489
+ has_participant: CHEBI:49067
+ univalent carbothioacylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an univalent carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a divalent carbothioacyl group.
+ divalent carbothioacylation
+ MOP:0000490
+ has_participant: CHEBI:49068
+ divalent carbothioacylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a divalent carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a carbonimidoyl group.
+ carbonimidoylation
+ MOP:0000491
+ has_participant: CHEBI:29815
+ carbonimidoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a carbonimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a thiocarbonyl group.
+ thiocarbonylation
+ MOP:0000492
+ has_participant: CHEBI:30256
+ thiocarbonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a thiocarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a (fluoren-9-ylmethoxy)carbonyl group.
+ (fluoren-9-ylmethoxy)carbonylation
+ MOP:0000493
+ has_participant: CHEBI:48605
+ (fluoren-9-ylmethoxy)carbonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a (fluoren-9-ylmethoxy)carbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a carbonyl group.
+ carbonylation
+ MOP:0000494
+ has_participant: CHEBI:23019
+ carbonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a carbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cytosin-1-yl group.
+ cytosin-1-ylation
+ MOP:0000495
+ has_participant: CHEBI:30758
+ cytosin-1-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cytosin-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a thymin-1-yl group.
+ thymin-1-ylation
+ MOP:0000496
+ has_participant: CHEBI:30757
+ thymin-1-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a thymin-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an uracil-1-yl group.
+ uracil-1-ylation
+ MOP:0000497
+ has_participant: CHEBI:30759
+ uracil-1-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an uracil-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a morpholin-4-ylsulfonyl group.
+ morpholin-4-ylsulfonylation
+ MOP:0000498
+ has_participant: CHEBI:45701
+ morpholin-4-ylsulfonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a morpholin-4-ylsulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an acetohydrazonoyl group.
+ acetohydrazonoylation
+ MOP:0000499
+ has_participant: CHEBI:48054
+ acetohydrazonoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an acetohydrazonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-hydroxyethyl group.
+ 2-hydroxyethylation
+ MOP:0000500
+ has_participant: CHEBI:44730
+ 2-hydroxyethylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a 2-hydroxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an aminosulfinyl group.
+ aminosulfinylation
+ MOP:0000501
+ has_participant: CHEBI:48257
+ aminosulfinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an aminosulfinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a disiloxanyl group.
+ disiloxanylation
+ MOP:0000502
+ has_participant: CHEBI:48142
+ disiloxanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a disiloxanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a disiloxane-1,3-diyl group.
+ disiloxane-1,3-diylation
+ MOP:0000503
+ has_participant: CHEBI:48143
+ disiloxane-1,3-diylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a disiloxane-1,3-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an azinoyl group.
+ azinoylation
+ MOP:0000504
+ has_participant: CHEBI:29771
+ azinoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an azinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an azonoyl group.
+ azonoylation
+ MOP:0000505
+ has_participant: CHEBI:37768
+ azonoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an azonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a phosphorothioyl group.
+ phosphorothioylation
+ MOP:0000506
+ has_participant: CHEBI:32412
+ phosphorothioylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a phosphorothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a phosphonothioyl group.
+ phosphonothioylation
+ MOP:0000507
+ has_participant: CHEBI:32413
+ phosphonothioylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a phosphonothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an arsonoyl group.
+ arsonoylation
+ MOP:0000508
+ has_participant: CHEBI:29848
+ arsonoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an arsonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an arsinoyl group.
+ arsinoylation
+ MOP:0000509
+ has_participant: CHEBI:30277
+ arsinoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an arsinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a stiboryl group.
+ stiborylation
+ MOP:0000510
+ has_participant: CHEBI:48439
+ stiborylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a stiboryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfamoyl group.
+ sulfamoylation
+ MOP:0000511
+ has_participant: CHEBI:48266
+ sulfamoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a S-aminosulfinimidoyl group.
+ S-aminosulfinimidoylation
+ MOP:0000512
+ has_participant: CHEBI:48254
+ S-aminosulfinimidoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a S-aminosulfinimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a S-aminosulfonimidoyl group.
+ S-aminosulfonimidoylation
+ MOP:0000513
+ has_participant: CHEBI:48264
+ S-aminosulfonimidoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a S-aminosulfonimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a chloryl group.
+ chlorylation
+ MOP:0000514
+ has_participant: CHEBI:29883
+ chlorylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a chloryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a chlorosyl group.
+ chlorosylation
+ MOP:0000515
+ has_participant: CHEBI:29878
+ chlorosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a chlorosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a perchloryl group.
+ perchlorylation
+ MOP:0000516
+ has_participant: CHEBI:29877
+ perchlorylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a perchloryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a bromosyl group.
+ bromosylation
+ MOP:0000517
+ has_participant: CHEBI:29871
+ bromosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a bromosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a bromyl group.
+ bromylation
+ MOP:0000518
+ has_participant: CHEBI:29881
+ bromylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a bromyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a perbromyl group.
+ perbromylation
+ MOP:0000519
+ has_participant: CHEBI:29891
+ perbromylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a perbromyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an iodosyl group.
+ iodosylation
+ MOP:0000520
+ has_participant: CHEBI:29897
+ iodosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an iodosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an iodyl group.
+ iodylation
+ MOP:0000521
+ has_participant: CHEBI:29904
+ iodylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an iodyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a periodyl group.
+ periodylation
+ MOP:0000522
+ has_participant: CHEBI:29908
+ periodylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a periodyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a fluorosyl group.
+ fluorosylation
+ MOP:0000523
+ has_participant: CHEBI:30241
+ fluorosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a fluorosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an acetoxysulfonyl group.
+ acetoxysulfonylation
+ MOP:0000525
+ has_participant: CHEBI:48065
+ acetoxysulfonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an acetoxysulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfonothioyl group.
+ sulfonothioylation
+ MOP:0000526
+ has_participant: CHEBI:29828
+ sulfonothioylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfonothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfinothioyl group.
+ sulfinothioylation
+ MOP:0000527
+ has_participant: CHEBI:29827
+ sulfinothioylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfinothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfonodithioyl group.
+ sulfonodithioylation
+ MOP:0000528
+ has_participant: CHEBI:29835
+ sulfonodithioylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfonodithioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a trioxidanyl group.
+ trioxidanylation
+ MOP:0000529
+ has_participant: CHEBI:29791
+ trioxidanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a trioxidanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a trioxidanediyl group.
+ trioxidanediylation
+ MOP:0000530
+ has_participant: CHEBI:30493
+ trioxidanediylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a trioxidanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a heterocyclyl group.
+ heterocyclylation
+ MOP:0000531
+ has_participant: CHEBI:48271
+ heterocyclylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a heterocyclyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a phosphoramidochloridoyl group.
+ phosphoramidochloridoylation
+ MOP:0000532
+ has_participant: CHEBI:48229
+ phosphoramidochloridoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a phosphoramidochloridoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a S-aminosulfonodiimidoyl group.
+ S-aminosulfonodiimidoylation
+ MOP:0000533
+ has_participant: CHEBI:48265
+ S-aminosulfonodiimidoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a S-aminosulfonodiimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an aminosulfanyl group.
+ aminosulfanylation
+ MOP:0000534
+ has_participant: CHEBI:48252
+ aminosulfanylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an aminosulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfinyl group.
+ sulfinylation
+ MOP:0000535
+ has_participant: CHEBI:29822
+ sulfinylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an arsoryl group.
+ arsorylation
+ MOP:0000536
+ has_participant: CHEBI:30274
+ arsorylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an arsoryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an azanediidyl group.
+ azanediidylation
+ MOP:0000537
+ has_participant: CHEBI:30227
+ azanediidylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an azanediidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfinimidoyl group.
+ sulfinimidoylation
+ MOP:0000538
+ has_participant: CHEBI:29829
+ sulfinimidoylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfinimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfonyl group.
+ MOP:0000524
+ sulfonylation
+ MOP:0000539
+ sulfonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a tosyl group.
+ tosylation
+ MOP:0000540
+ has_participant: CHEBI:51094
+ tosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a tosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a brosyl group.
+ brosylation
+ MOP:0000541
+ has_participant: CHEBI:51101
+ brosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a brosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a nosyl group.
+ nosylation
+ MOP:0000542
+ has_participant: CHEBI:51102
+ nosylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a nosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A process in which at least one of the participants is a molecule.
+ MOP:0000543
+ TODO: needs work, formal definition, etc.
+ molecular process
+
+
+
+
+ A process in which at least one of the participants is a molecule.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an indolyl group.
+ MOP:0000544
+ has_participant: CHEBI:51609
+ indolylamination
+
+
+
+
+ Formation of a covalent bond between a substrate and an indolyl group.
+ RSC:xp
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an indol-1-yl group.
+ MOP:0000545
+ has_participant: CHEBI:51610
+ indol-1-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an indol-1-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an indol-2-yl group.
+ MOP:0000546
+ has_participant: CHEBI:51611
+ indol-2-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an indol-2-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an indol-3-yl group.
+ MOP:0000547
+ has_participant: CHEBI:51612
+ indol-3-ylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an indol-3-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-oxindolyl group.
+ MOP:0000548
+ has_participant: CHEBI:51613
+ N-oxindolylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an N-oxindolyl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alkylamino group.
+ MOP:0000549
+ has_participant: CHEBI:22332
+ alkylamination
+
+
+
+
+ Formation of a covalent bond between a substrate and an alkylamino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a halo group.
+ MOP:0000550
+ has_participant: CHEBI:47854
+ halogenation
+
+
+
+
+ Formation of a covalent bond between a substrate and a halo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a bromo group.
+ MOP:0000551
+ has_participant: CHEBI:47265
+ bromination
+
+
+
+
+ Formation of a covalent bond between a substrate and a bromo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a chloro group.
+ MOP:0000552
+ has_participant: CHEBI:47853
+ chlorination
+
+
+
+
+ Formation of a covalent bond between a substrate and a chloro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a fluoro group.
+ MOP:0000553
+ has_participant: CHEBI:42645
+ fluorination
+
+
+
+
+ Formation of a covalent bond between a substrate and a fluoro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an iodo group.
+ MOP:0000554
+ has_participant: CHEBI:43448
+ iodination
+
+
+
+
+ Formation of a covalent bond between a substrate and an iodo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an imino group.
+ MOP:0000555
+ has_participant: CHEBI:29342
+ imination
+
+
+
+
+ Formation of a covalent bond between a substrate and an imino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a nitro group.
+ MOP:0000556
+ has_participant: CHEBI:29785
+ nitration
+
+
+
+
+ Formation of a covalent bond between a substrate and a nitro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a hydroxyamino group.
+ MOP:0000557
+ has_participant: CHEBI:29769
+ hydroxyamination
+
+
+
+
+ Formation of a covalent bond between a substrate and a hydroxyamino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a thioxo group.
+ MOP:0000558
+ has_participant: CHEBI:29833
+ thioxonation
+
+
+
+
+ Formation of a covalent bond between a substrate and a thioxo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfo group.
+ hydroxysulfonylation
+ MOP:0000559
+ has_participant: CHEBI:29922
+ sulfonation
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a selenono group.
+ MOP:0000560
+ has_participant: CHEBI:29923
+ selenonation
+
+
+
+
+ Formation of a covalent bond between a substrate and a selenono group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a ring in a molecule from a chain by formation of a new bond.
+ cyclisation
+ MOP:0000561
+ cyclization
+
+
+
+
+ Formation of a ring in a molecule from a chain by formation of a new bond.
+ https://doi.org/10.1351/goldbook.C01494
+
+
+
+
+
+
+
+
+ A molecular process where two or more unsaturated molecules or parts of the same molecule combine to form a cyclic adduct in which there is a net reduction of bond multiplicity.
+ MOP:0000562
+ cycloaddition
+
+
+
+
+ A molecular process where two or more unsaturated molecules or parts of the same molecule combine to form a cyclic adduct in which there is a net reduction of bond multiplicity.
+ https://doi.org/10.1351/goldbook.C01496
+
+
+
+
+
+
+
+
+ A cycloaddition in which each participant contributes two electrons to the transformation of reactants to products.
+ MOP:0000563
+ [2+2] cycloaddition
+
+
+
+
+ A cycloaddition in which each participant contributes two electrons to the transformation of reactants to products.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A molecular process in which a cyclic system decomposes into two or more unsaturated molecules or parts of the same molecule and there is a net increase in bond multiplicity.
+ cycloreversion
+ retro-addition
+ retrocycloaddtion
+ MOP:0000564
+ cycloelimination
+
+
+
+
+ A molecular process in which a cyclic system decomposes into two or more unsaturated molecules or parts of the same molecule and there is a net increase in bond multiplicity.
+ https://doi.org/10.1351/goldbook.C01496
+ https://doi.org/10.1351/goldbook.C01501
+
+
+
+
+ cycloreversion
+ https://doi.org/10.1351/goldbook.C01506
+
+
+
+
+ retrocycloaddtion
+ https://doi.org/10.1351/goldbook.R05372
+
+
+
+
+
+
+
+
+ A cycloaddition in which one participant contributes four electrons and the other participant contributes two electrons to the transformation of reactants to products.
+ MOP:0000565
+ [4+2] cycloaddition
+
+
+
+
+ A cycloaddition in which one participant contributes four electrons and the other participant contributes two electrons to the transformation of reactants to products.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a group.
+ batchelorc
+ 2009-04-22T10:01:32Z
+ MOP:0000566
+ formation of covalent bond with group
+
+
+
+
+ Formation of a covalent bond between a substrate and a group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a group.
+ batchelorc
+ 2009-04-30T02:24:32Z
+ MOP:0000567
+ breaking of covalent bond with group
+
+
+
+
+ Breaking of a covalent bond between a substrate and a group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ The complete, net removal of one or mole electrons from a molecular entity, corresponding to an increase in the oxidation number of any atom within any substrate.
+ batchelorc
+ 2009-06-01T06:01:47Z
+ de-electronation
+ MOP:0000568
+ oxidation
+
+
+
+
+ The complete, net removal of one or mole electrons from a molecular entity, corresponding to an increase in the oxidation number of any atom within any substrate.
+ https://doi.org/10.1351/goldbook.O04362
+
+
+
+
+
+
+
+
+ The complete transfer of one or more electrons to a molecular entity.
+ batchelorc
+ 2009-06-01T06:04:18Z
+ electronation
+ MOP:0000569
+ reduction
+
+
+
+
+ The complete transfer of one or more electrons to a molecular entity.
+ https://doi.org/10.1351/goldbook.R05222
+
+
+
+
+
+
+
+
+ The transfer of an electron to a molecular entity, resulting in a molecular entity of increased negative charge.
+ batchelorc
+ 2009-06-01T06:06:19Z
+ MOP:0000570
+ electron attachment
+
+
+
+
+ The transfer of an electron to a molecular entity, resulting in a molecular entity of increased negative charge.
+ https://doi.org/10.1351/goldbook.E01979
+
+
+
+
+
+
+
+
+ A reduction in which an aldehyde is reduced to form a primary alcohol.
+ batchelorc
+ 2009-06-01T06:07:02Z
+ MOP:0000571
+ aldehyde reduction
+
+
+
+
+ A reduction in which an aldehyde is reduced to form a primary alcohol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An oxidation process where an alcohol is transformed into a carbonyl compound.
+ batchelorc
+ 2009-06-01T06:10:35Z
+ MOP:0000572
+ alcohol oxidation
+
+
+
+
+ An oxidation process where an alcohol is transformed into a carbonyl compound.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An oxidation process where a primary alcohol is transformed into an aldehyde.
+ batchelorc
+ 2009-06-01T06:10:59Z
+ MOP:0000573
+ primary alcohol oxidation
+
+
+
+
+ An oxidation process where a primary alcohol is transformed into an aldehyde.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An oxidation process where a secondary alcohol is transformed into a ketone.
+ batchelorc
+ 2009-06-01T06:11:31Z
+ MOP:0000574
+ secondary alcohol oxidation
+
+
+
+
+ An oxidation process where a secondary alcohol is transformed into a ketone.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An oxidation process where an amine is transformed into an imine.
+ batchelorc
+ 2009-06-01T06:15:40Z
+ MOP:0000575
+ amine oxidation
+
+
+
+
+ An oxidation process where an amine is transformed into an imine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A reduction process where an imine is transformed into an amine.
+ batchelorc
+ 2009-06-01T06:19:21Z
+ MOP:0000576
+ imine reduction
+
+
+
+
+ A reduction process where an imine is transformed into an amine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A reduction process where the oxidation state carbonyl carbon in the ester functionality is reduced.
+ batchelorc
+ 2009-06-02T05:30:48Z
+ reduction of ester
+ MOP:0000577
+ ester reduction
+
+
+
+
+ A reduction process where the oxidation state carbonyl carbon in the ester functionality is reduced.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An ester reduction where the product is the corresponding aldehyde.
+ batchelorc
+ 2009-06-02T05:31:49Z
+ reduction of ester to aldehyde
+ reduction of esters to aldehyde
+ MOP:0000578
+ ester reduction to aldehyde
+
+
+
+
+ An ester reduction where the product is the corresponding aldehyde.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An ester reduction where the product is the corresponding primary alcohol.
+ batchelorc
+ 2009-06-02T05:32:37Z
+ reduction of ester to primary alcohol
+ reduction of esters to primary alcohol
+ MOP:0000579
+ ester reduction to primary alcohol
+
+
+
+
+ An ester reduction where the product is the corresponding primary alcohol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A reduction process where a ketone is reduced to a secondary alcohol.
+ batchelorc
+ 2009-06-02T05:35:42Z
+ reduction of ketone
+ reduction of ketones
+ MOP:0000580
+ ketone reduction
+
+
+
+
+ A reduction process where a ketone is reduced to a secondary alcohol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An oxidation process where the oxidation state of at least one doubly-bonded carbon atom increases.
+ batchelorc
+ 2009-06-02T05:45:30Z
+ olefin oxidation
+ MOP:0000581
+ alkene oxidation
+
+
+
+
+ An oxidation process where the oxidation state of at least one doubly-bonded carbon atom increases.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An alkene oxidation where the product is the corresponding 1,2-diol.
+ batchelorc
+ 2009-06-02T05:46:52Z
+ alkene oxidation to glycol
+ oxidation of alkene to 1,2-diol
+ oxidation of alkenes to 1,2-diol
+ MOP:0000582
+ alkene oxidation to 1,2-diol
+
+
+
+
+ An alkene oxidation where the product is the corresponding 1,2-diol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An alkene oxidation where the reagent is ozone and the product is the corresponding ozonide.
+ batchelorc
+ 2009-06-02T05:48:42Z
+ ozonolysis of alkene
+ ozonolysis of alkenes
+ MOP:0000583
+ alkene ozonolysis
+
+
+
+
+ An alkene oxidation where the reagent is ozone and the product is the corresponding ozonide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ An alkene oxidation process where the reactant is a primary alkene and the products are carboxylic acid and carbon dioxide. This can be achieved with a warm, acidic solution of potassium permanganate.
+ batchelorc
+ 2009-06-02T06:02:46Z
+ MOP:0000584
+ primary alkene oxidation to carboxylic acid and carbon dioxide
+
+
+
+
+ An alkene oxidation process where the reactant is a primary alkene and the products are carboxylic acid and carbon dioxide. This can be achieved with a warm, acidic solution of potassium permanganate.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ An alkene oxidation where the reactant is a tertiary alkene and the products are the corresponding carboxylic acid and ketone. This can be achieved with a warm, acidic solution of potassium permanganate.
+ batchelorc
+ 2009-06-02T06:04:14Z
+ MOP:0000585
+ tertiary alkene oxidation to carboxylic acid and ketone
+
+
+
+
+ An alkene oxidation where the reactant is a tertiary alkene and the products are the corresponding carboxylic acid and ketone. This can be achieved with a warm, acidic solution of potassium permanganate.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ An alkene oxidation process where the reactant is a secondary alkene and the products are the corresponding aldehydes. This can be achieved with warm, acidic potassium permanganate.
+ batchelorc
+ 2009-06-02T06:06:23Z
+ MOP:0000586
+ secondary, non-terminal alkene oxidation to aldehydes
+
+
+
+
+ An alkene oxidation process where the reactant is a secondary alkene and the products are the corresponding aldehydes. This can be achieved with warm, acidic potassium permanganate.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ An alkene oxidation process where the reactant is a secondary terminal alkene and the products are carbon dioxide and the corresponding ketone. This can be achieved by warm, acidic potassium permanganate solution.
+ batchelorc
+ 2009-06-02T06:07:44Z
+ MOP:0000587
+ secondary terminal alkene oxidation to ketone and carbon dioxide
+
+
+
+
+ An alkene oxidation process where the reactant is a secondary terminal alkene and the products are carbon dioxide and the corresponding ketone. This can be achieved by warm, acidic potassium permanganate solution.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ An alkene oxidation process where the reactant is a quaternary alkene and the products are the corresponding ketones.
+ batchelorc
+ 2009-06-02T06:09:24Z
+ MOP:0000588
+ quaternary alkene oxidation to ketones
+
+
+
+
+ An alkene oxidation process where the reactant is a quaternary alkene and the products are the corresponding ketones.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A reduction process that involves addition of hydrogen atoms across a double bond.
+ batchelorc
+ 2009-06-05T04:53:34Z
+ MOP:0000589
+ hydrogenation
+
+
+
+
+ A reduction process that involves addition of hydrogen atoms across a double bond.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An oxidation process that involves the removal of adjacent hydrogen atoms, resulting in an increase of bond order.
+ batchelorc
+ 2009-06-05T04:54:48Z
+ MOP:0000590
+ dehydrogenation
+
+
+
+
+ An oxidation process that involves the removal of adjacent hydrogen atoms, resulting in an increase of bond order.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a carboxy group.
+ batchelorc
+ 2009-06-05T04:57:07Z
+ MOP:0000591
+ CHEBI:46883.
+ carboxylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a carboxy group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carboxy group.
+ batchelorc
+ 2009-06-05T04:59:02Z
+ MOP:0000592
+ C-carboxylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carboxy group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carboxy group.
+ batchelorc
+ 2009-06-05T05:00:09Z
+ MOP:0000593
+ N-carboxylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carboxy group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carboxy group.
+ batchelorc
+ 2009-06-05T05:00:57Z
+ MOP:0000594
+ O-carboxylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carboxy group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carboxy group.
+ batchelorc
+ 2009-06-05T05:01:43Z
+ MOP:0000595
+ S-carboxylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carboxy group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a pseudohalo group.
+ MOP:0000596
+ pseudohalogenation
+
+
+
+
+ Formation of a covalent bond between a substrate and a pseudohalo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a cyano group.
+ MOP:0000597
+ cyanation
+
+
+
+
+ Formation of a covalent bond between a substrate and a cyano group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a azido group.
+ MOP:0000598
+ azidation
+
+
+
+
+ Formation of a covalent bond between a substrate and a azido group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an isocyano group.
+ MOP:0000599
+ isocyanation
+
+
+
+
+ Formation of a covalent bond between a substrate and an isocyano group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an isocyanato group.
+ MOP:0000600
+ isocyanatation
+
+
+
+
+ Formation of a covalent bond between a substrate and an isocyanato group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an isothiocyanate group.
+ MOP:0000601
+ isothiocyanatation
+
+
+
+
+ Formation of a covalent bond between a substrate and an isothiocyanate group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an isoselenocyanate group.
+ MOP:0000602
+ isoselenocyanatation
+
+
+
+
+ Formation of a covalent bond between a substrate and an isoselenocyanate group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an isotellurocyanate group.
+ MOP:0000603
+ isotellurocyanatation
+
+
+
+
+ Formation of a covalent bond between a substrate and an isotellurocyanate group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ The formation of at least two single bonds between a metal atom and a ligand.
+ batchelorc
+ 2009-08-14T09:55:35Z
+ metal ion chelation
+ MOP:0000604
+ metal chelation
+
+
+
+
+ The formation of at least two single bonds between a metal atom and a ligand.
+ https://doi.org/10.1351/goldbook.C01012
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Metal chelation where the metal atom is an iron atom.
+ batchelorc
+ 2009-08-14T09:57:15Z
+ MOP:0000605
+ iron chelation
+
+
+
+
+ Metal chelation where the metal atom is an iron atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Iron chelation where the iron atom has a charge of +2.
+ batchelorc
+ 2009-08-14T09:59:38Z
+ MOP:0000606
+ iron(2+) chelation
+
+
+
+
+ Iron chelation where the iron atom has a charge of +2.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Iron chelation where the iron atom has a charge of +3.
+ batchelorc
+ 2009-08-14T10:00:03Z
+ MOP:0000607
+ iron(3+) chelation
+
+
+
+
+ Iron chelation where the iron atom has a charge of +3.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Metal chelation where the metal atom is a copper atom.
+ batchelorc
+ 2009-08-14T10:11:34Z
+ MOP:0000608
+ copper chelation
+
+
+
+
+ Metal chelation where the metal atom is a copper atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Metal chelation where the metal atom is a zinc atom.
+ batchelorc
+ 2009-08-14T10:12:01Z
+ MOP:0000609
+ zinc chelation
+
+
+
+
+ Metal chelation where the metal atom is a zinc atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Metal chelation where the metal atom is a lead atom.
+ batchelorc
+ 2009-08-14T10:13:11Z
+ MOP:0000610
+ lead chelation
+
+
+
+
+ Metal chelation where the metal atom is a lead atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Metal chelation where the metal atom is a cobalt atom.
+ batchelorc
+ 2009-08-14T10:14:05Z
+ MOP:0000611
+ cobalt chelation
+
+
+
+
+ Metal chelation where the metal atom is a cobalt atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Metal chelation where the metal atom is an aluminium atom.
+ batchelorc
+ 2009-08-14T10:14:29Z
+ MOP:0000612
+ aluminium chelation
+
+
+
+
+ Metal chelation where the metal atom is an aluminium atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Metal chelation where the metal atom is a molybdenum atom.
+ batchelorc
+ 2009-08-14T10:17:50Z
+ MOP:0000613
+ molybdenum chelation
+
+
+
+
+ Metal chelation where the metal atom is a molybdenum atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Metal chelation where the metal atom is a plutonium atom.
+ batchelorc
+ 2009-08-14T10:24:18Z
+ MOP:0000614
+ plutonium chelation
+
+
+
+
+ Metal chelation where the metal atom is a plutonium atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A process where an electron is transferred from one molecular entity or part of a molecular entity to a different molecular entity or part of the same molecular entity.
+ batchelorc
+ 2009-09-15T03:55:41Z
+ MOP:0000615
+ electron transfer
+
+
+
+
+ A process where an electron is transferred from one molecular entity or part of a molecular entity to a different molecular entity or part of the same molecular entity.
+ https://doi.org/10.1351/goldbook.E02011
+
+
+
+
+
+
+
+
+ An electron transfer reaction that involves a small change in free energy compared to kT. The product distribution of the equilibrium corresponding to this reaction will be a mixture of similar quantities of reactant and product.
+ batchelorc
+ 2009-09-15T04:27:03Z
+ MOP:0000616
+ reversible electron transfer
+
+
+
+
+ An electron transfer reaction that involves a small change in free energy compared to kT. The product distribution of the equilibrium corresponding to this reaction will be a mixture of similar quantities of reactant and product.
+ RSC:crb
+
+
+
+
+
+
+
+
+ An electron transfer reaction that involves a large change in free energy compared to kT. The product distribution of an equilibrium corresponding to this reaction will mainly consist of the product.
+ batchelorc
+ 2009-09-15T04:31:22Z
+ MOP:0000617
+ irreversible electron transfer
+
+
+
+
+ An electron transfer reaction that involves a large change in free energy compared to kT. The product distribution of an equilibrium corresponding to this reaction will mainly consist of the product.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A molecular process where a molecule is broken up by reaction with a molecule that is part of the solvent material. It may be the primary constituent molecule of the solvent material (for example water, ethanol, ammonia) or its lyonium ion or lyate ion.
+ batchelorc
+ 2009-09-16T11:11:24Z
+ MOP:0000618
+ solvolysis
+
+
+
+
+ A molecular process where a molecule is broken up by reaction with a molecule that is part of the solvent material. It may be the primary constituent molecule of the solvent material (for example water, ethanol, ammonia) or its lyonium ion or lyate ion.
+ https://doi.org/10.1351/goldbook.S05762
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A solvolysis reaction where the solvent material is water.
+ batchelorc
+ 2009-09-16T11:13:21Z
+ MOP:0000619
+ hydrolysis
+
+
+
+
+ A solvolysis reaction where the solvent material is water.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A solvolysis reaction where the solvent material is an alcohol.
+ batchelorc
+ 2009-09-16T11:14:18Z
+ MOP:0000620
+ alcoholysis
+
+
+
+
+ A solvolysis reaction where the solvent material is an alcohol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A solvolysis reaction where the solvent material is an amine.
+ batchelorc
+ 2009-09-16T11:15:07Z
+ MOP:0000621
+ aminolysis
+
+
+
+
+ A solvolysis reaction where the solvent material is an amine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A solvolysis reaction where the solvent material is ammonia.
+ batchelorc
+ 2009-09-16T11:17:31Z
+ ammoniolysis
+ MOP:0000622
+ ammonolysis
+
+
+
+
+ A solvolysis reaction where the solvent material is ammonia.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An alcoholysis reaction where the solvent alcohol is methanol.
+ batchelorc
+ 2009-09-16T11:21:09Z
+ MOP:0000623
+ methanolysis
+
+
+
+
+ An alcoholysis reaction where the solvent alcohol is methanol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An alcoholysis reaction where the solvent alcohol is ethanol.
+ batchelorc
+ 2009-09-16T11:21:36Z
+ MOP:0000624
+ ethanolysis
+
+
+
+
+ An alcoholysis reaction where the solvent alcohol is ethanol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An alcoholysis reaction where the solvent alcohol is a propanol.
+ batchelorc
+ 2009-09-16T11:22:06Z
+ MOP:0000625
+ propanolysis
+
+
+
+
+ An alcoholysis reaction where the solvent alcohol is a propanol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An alcoholysis reaction where the solvent alcohol is a butanol.
+ batchelorc
+ 2009-09-16T11:22:36Z
+ MOP:0000626
+ butanolysis
+
+
+
+
+ An alcoholysis reaction where the solvent alcohol is a butanol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A reaction in which two or more reactants or remote reactive sites within the same molecular entity yield a single main product with accompanying formation of a small molecule.
+ batchelorc
+ 2009-09-16T11:30:32Z
+ MOP:0000627
+ condensation reaction
+
+
+
+
+ A reaction in which two or more reactants or remote reactive sites within the same molecular entity yield a single main product with accompanying formation of a small molecule.
+ https://doi.org/10.1351/goldbook.C01238
+
+
+
+
+
+
+
+
+ A condensation reaction where the small molecule produced is water.
+ batchelorc
+ 2009-09-16T11:32:33Z
+ MOP:0000628
+ dehydration reaction
+
+
+
+
+ A condensation reaction where the small molecule produced is water.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The process of converting a monomer mixture of monomers into a polymer.
+ polymerization
+ MOP:0000629
+ polymerisation
+
+
+
+
+ The process of converting a monomer mixture of monomers into a polymer.
+ https://doi.org/10.1351/goldbook.P04740
+
+
+
+
+
+
+
+
+ The process of converting a polymer into a monomer or mixture of monomers.
+ depolymerization
+ MOP:0000630
+ depolymerisation
+
+
+
+
+ The process of converting a polymer into a monomer or mixture of monomers.
+ https://doi.org/10.1351/goldbook.D01600
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A polymerisation in which a copolymer is formed.
+ copolymerization
+ MOP:0000631
+ copolymerisation
+
+
+
+
+ A polymerisation in which a copolymer is formed.
+ https://doi.org/10.1351/goldbook.C01336
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Polymerisation by a repeated condensation process.
+ condensation polymerization
+ MOP:0000632
+ condensation polymerisation
+
+
+
+
+ Polymerisation by a repeated condensation process.
+ https://doi.org/10.1351/goldbook.C01237
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Polymerisation in which a homopolymer is formed.
+ homopolymerization
+ MOP:0000633
+ homopolymerisation
+
+
+
+
+ Polymerisation in which a homopolymer is formed.
+ https://doi.org/10.1351/goldbook.H02855
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A chain reaction in which the growth of a polymer chain proceeds exclusively by reaction(s) between monomer(s) and reactive site(s) on the polymer chain with regeneration of the reactive site(s) at the end of each growth step.
+ MOP:0000634
+ has_part only some particular polymerisation step rather than some other polymerisation step.
+ chain polymerisation
+
+
+
+
+ A chain reaction in which the growth of a polymer chain proceeds exclusively by reaction(s) between monomer(s) and reactive site(s) on the polymer chain with regeneration of the reactive site(s) at the end of each growth step.
+ https://doi.org/10.1351/goldbook.C00958
+
+
+
+
+
+
+
+
+ A reaction in which one or more reactive reaction intermediates (frequently radicals) are continuously regenerated, usually through a repetitive cycle of elementary steps (the 'propagation step').
+ MOP:0000635
+ chain reaction
+
+
+
+
+ A reaction in which one or more reactive reaction intermediates (frequently radicals) are continuously regenerated, usually through a repetitive cycle of elementary steps (the 'propagation step').
+ https://doi.org/10.1351/goldbook.C00960
+
+
+
+
+
+
+
+
+ An ionic polymerisation in which the active centres are anionic.
+ anionic polymerization
+ MOP:0000636
+ anionic polymerisation
+
+
+
+
+ An ionic polymerisation in which the active centres are anionic.
+ https://doi.org/10.1351/goldbook.A00361
+
+
+
+
+
+
+
+
+ A chain polymerisation in which the active centres are ions or ion pairs.
+ ionic polymerization
+ MOP:0000637
+ ionic polymerisation
+
+
+
+
+ A chain polymerisation in which the active centres are ions or ion pairs.
+ https://doi.org/10.1351/goldbook.I03178
+
+
+
+
+
+
+
+
+ An ionic polymerisation in which the active centres are cationic.
+ cationic polymerization
+ MOP:0000638
+ cationic polymerisation
+
+
+
+
+ An ionic polymerisation in which the active centres are cationic.
+ https://doi.org/10.1351/goldbook.C00910
+
+
+
+
+
+
+
+
+ A chain polymerisation in which the active centres are radicals. Usually the growing chain end bears an unpaired electron.
+ free radical polymerisation
+ free radical polymerization
+ radical polymerization
+ MOP:0000639
+ radical polymerisation
+
+
+
+
+ A chain polymerisation in which the active centres are radicals. Usually the growing chain end bears an unpaired electron.
+ https://doi.org/10.1351/goldbook.R05075
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A molecular process in which an initiating species adds to a monomer to form a chain carrier.
+ MOP:0000640
+ chain initiation
+
+
+
+
+ A molecular process in which an initiating species adds to a monomer to form a chain carrier.
+ https://doi.org/10.1351/goldbook.C00955
+
+
+
+
+
+
+
+
+ A polymerisation where the growth of polymer chains proceeds by reactions between all degrees of polymerisation.
+ all-degree polymerization
+ MOP:0000641
+ all-degree polymerisation
+
+
+
+
+ A polymerisation where the growth of polymer chains proceeds by reactions between all degrees of polymerisation.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A reaction of two or more reacting molecular entities resulting in a single reaction product containing all atoms of all components with formation of two chemical bonds and a net reduction in bond multiplicity.
+ MOP:0000642
+ addition reaction
+
+
+
+
+ A reaction of two or more reacting molecular entities resulting in a single reaction product containing all atoms of all components with formation of two chemical bonds and a net reduction in bond multiplicity.
+ https://doi.org/10.1351/goldbook.A00133
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An all-degree polymerisation that proceeds by addition reactions.
+ MOP:0000643
+ polyaddition
+
+
+
+
+ An all-degree polymerisation that proceeds by addition reactions.
+ https://doi.org/10.1351/goldbook.P04720
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An all-degree polymerisation that proceeds by condensation reactions.
+ MOP:0000644
+ polycondensation
+
+
+
+
+ An all-degree polymerisation that proceeds by condensation reactions.
+ https://doi.org/10.1351/goldbook.P04722
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A chain polymerisation that proceeds by condensation steps.
+ MOP:0000645
+ condensative chain polymerisation
+
+
+
+
+ A chain polymerisation that proceeds by condensation steps.
+ https://doi.org/10.1351/goldbook.C01239
+
+
+
+
+
+
+
+
+ A chain polymerisation that consists only of chain initiation and chain propagation steps.
+ living polymerization
+ MOP:0000646
+ living polymerisation
+
+
+
+
+ A chain polymerisation that consists only of chain initiation and chain propagation steps.
+ https://doi.org/10.1351/goldbook.L03597
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An ionic polymerisation where the product is a copolymer.
+ ionic copolymerization
+ MOP:0000647
+ ionic copolymerisation
+
+
+
+
+ An ionic polymerisation where the product is a copolymer.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A radical polymerisation where the product is a copolymer.
+ free radical copolymerisation
+ free radical copolymerization
+ radical copolymerization
+ MOP:0000648
+ radical copolymerisation
+
+
+
+
+ A radical polymerisation where the product is a copolymer.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A living polymerisation where the product is a copolymer.
+ MOP:0000649
+ living copolymerisation
+
+
+
+
+ A living polymerisation where the product is a copolymer.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an amino group.
+ MOP:0000650
+ amination
+
+
+
+
+ Formation of a covalent bond between a substrate and an amino group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an amino group.
+ MOP:0000651
+ deamination
+
+
+
+
+ Breaking of a covalent bond between a substrate and an amino group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an amino group.
+ MOP:0000652
+ N-amination
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an amino group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an amino group.
+ MOP:0000653
+ O-amination
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an amino group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an amino group.
+ MOP:0000654
+ C-amination
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an amino group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an amino group.
+ MOP:0000655
+ S-amination
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an amino group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A molecular process where two groups are lost with concomitant formation of an unsaturation in the molecule or formation of a new ring.
+ MOP:0000656
+ elimination reaction
+
+
+
+
+ A molecular process where two groups are lost with concomitant formation of an unsaturation in the molecule or formation of a new ring.
+ https://doi.org/10.1351/goldbook.E02038
+
+
+
+
+
+
+
+
+ An elimination reaction where both groups are lost from the same atom.
+ 1,1-elimination
+ 1,1-elimination reaction
+ alpha-elimination
+ MOP:0000657
+ 1/1/elimination reaction
+
+
+
+
+ An elimination reaction where both groups are lost from the same atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An elimination reaction where the groups are lost from adjacent atoms.
+ 1,2-elimination
+ 1,2-elimination reaction
+ beta-elimination
+ MOP:0000658
+ 1/2/elimination reaction
+
+
+
+
+ An elimination reaction where the groups are lost from adjacent atoms.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An elimination reaction where the groups are lost from atoms that are 1,3- to each other.
+ 1,3-elimination
+ 1,3-elimination reaction
+ gamma-elimination
+ MOP:0000659
+ 1/3/elimination reaction
+
+
+
+
+ An elimination reaction where the groups are lost from atoms that are 1,3- to each other.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An elimination reaction where the groups are lost from atoms that are 1,4- to each other.
+ 1,4-elimination
+ 1,4-elimination reaction
+ delta-elimination
+ MOP:0000660
+ 1/4/elimination reaction
+
+
+
+
+ An elimination reaction where the groups are lost from atoms that are 1,4- to each other.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An elimination reaction where the groups are lost from atoms that are 1,5- to each other.
+ 1,5-elimination
+ 1,5-elimination reaction
+ epsilon-elimination
+ MOP:0000661
+ 1/5/elimination reaction
+
+
+
+
+ An elimination reaction where the groups are lost from atoms that are 1,5- to each other.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An elimination reaction where the groups are lost from atoms that are 1,6- to each other.
+ 1,6-elimination
+ 1,6-elimination reaction
+ MOP:0000662
+ 1/6/elimination reaction
+
+
+
+
+ An elimination reaction where the groups are lost from atoms that are 1,6- to each other.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An elimination reaction where the groups are lost from atoms that are 1,8- to each other.
+ 1,8-elimination
+ 1,8-elimination reaction
+ MOP:0000663
+ 1/8/elimination reaction
+
+
+
+
+ An elimination reaction where the groups are lost from atoms that are 1,8- to each other.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An addition reaction where the groups both add to the same atom.
+ 1,1-addition
+ 1,1-addition reaction
+ alpha-addition
+ MOP:0000664
+ 1/1/addition reaction
+
+
+
+
+ An addition reaction where the groups both add to the same atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An addition reaction where the groups add to adjacent atoms.
+ 1,2-addition
+ 1,2-addition reaction
+ beta-addition
+ MOP:0000665
+ 1/2/addition reaction
+
+
+
+
+ An addition reaction where the groups add to adjacent atoms.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An addition reaction where the groups add to atoms that are 1,3- to each other.
+ 1,3-addition
+ 1,3-addition reaction
+ gamma-addition
+ MOP:0000666
+ 1/3/addition reaction
+
+
+
+
+ An addition reaction where the groups add to atoms that are 1,3- to each other.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An addition reaction where the groups add to atoms that are 1,4- to each other.
+ 1,4-addition
+ 1,4-addition reaction
+ delta-addition
+ MOP:0000667
+ 1/4/addition reaction
+
+
+
+
+ An addition reaction where the groups add to atoms that are 1,4- to each other.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An addition reaction where the groups add to atoms that are 1,5- to each other.
+ 1,5-addition
+ 1,5-addition reaction
+ epsilon-addition
+ MOP:0000668
+ 1/5/addition reaction
+
+
+
+
+ An addition reaction where the groups add to atoms that are 1,5- to each other.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An addition reaction where the groups add to atoms that are 1,6- to each other.
+ 1,6-addition
+ 1,6-addition reaction
+ MOP:0000669
+ 1/6/addition reaction
+
+
+
+
+ An addition reaction where the groups add to atoms that are 1,6- to each other.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An addition reaction where the groups add to atoms that are 1,8- to each other.
+ 1,8-addition
+ 1,8-addition reaction
+ MOP:0000670
+ 1/8/addition reaction
+
+
+
+
+ An addition reaction where the groups add to atoms that are 1,8- to each other.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A molecular process that results in the formation of an epoxide.
+ MOP:0000671
+ epoxidation
+
+
+
+
+ A molecular process that results in the formation of an epoxide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A molecular process where a carbonyl compound is converted an enol. Usually this is a reversible tautomerization but it can be irreversible.
+ enolisation
+ MOP:0000672
+ enolization
+
+
+
+
+ A molecular process where a carbonyl compound is converted an enol. Usually this is a reversible tautomerization but it can be irreversible.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a hydroxy group.
+ MOP:0000673
+ hydroxylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a hydroxy group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a bond between a substrate and a metal atom.
+ metalation
+ MOP:0000674
+ has_participant metal atom when ChEBI get round to renaming those.
+ metallation
+
+
+
+
+ Formation of a bond between a substrate and a metal atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ Formation of two bonds between a metal atom and a substrate, resulting in a metallacycle.
+ cyclometalation
+ MOP:0000675
+ has_participant metal atom when ChEBI get round to renaming those.
+ cyclometallation
+
+
+
+
+ Formation of two bonds between a metal atom and a substrate, resulting in a metallacycle.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Breaking of a bond between a substrate and a metal atom.
+ demetalation
+ MOP:0000676
+ has_participant metal atom when ChEBI get round to renaming those.
+ demetallation
+
+
+
+
+ Breaking of a bond between a substrate and a metal atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Transfer of a metal atom from one substrate to another.
+ MOP:0000677
+ transmetallation
+
+
+
+
+ Transfer of a metal atom from one substrate to another.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ 1/2/addition across a double bond of a cyano group and a silyl group.
+ MOP:0000678
+ cyanosilylation
+
+
+
+
+ 1/2/addition across a double bond of a cyano group and a silyl group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A process where an electron pair is transferred from one molecular entity or part of a molecular entity to a different molecular entity or part of the same molecular entity.
+ MOP:0000679
+ electron pair transfer
+
+
+
+
+ A process where an electron pair is transferred from one molecular entity or part of a molecular entity to a different molecular entity or part of the same molecular entity.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A process where a proton is transferred from one binding site to another.
+ MOP:0000680
+ proton transfer
+
+
+
+
+ A process where a proton is transferred from one binding site to another.
+ https://doi.org/10.1351/goldbook.P04915
+
+
+
+
+
+
+
+
+ A proton transfer reaction between two identical molecules, one acting as a Broensted acid and the other as a Broensted base.
+ MOP:0000681
+ autoprotolysis
+
+
+
+
+ A proton transfer reaction between two identical molecules, one acting as a Broensted acid and the other as a Broensted base.
+ https://doi.org/10.1351/goldbook.A00351
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A process where a hydron is transferred from one binding site to another.
+ MOP:0000682
+ hydron transfer
+
+
+
+
+ A process where a hydron is transferred from one binding site to another.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A process where a deuteron is transferred from one binding site to another.
+ MOP:0000683
+ deuteron transfer
+
+
+
+
+ A process where a deuteron is transferred from one binding site to another.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A living polymerisation process where the chain initiation and chain propagation steps are atom transfer radical addition reactions. Often the atom transfer is a radical halogen atom and the reaction is catalysed by a transition metal species.
+ ATRP
+ atom-transfer radical polymerisation
+ MOP:0000684
+ atom-transfer radical polymerisation
+
+
+
+
+ A living polymerisation process where the chain initiation and chain propagation steps are atom transfer radical addition reactions. Often the atom transfer is a radical halogen atom and the reaction is catalysed by a transition metal species.
+ https://doi.org/10.1021/ja00125a035
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A ring-opening polymerisation that proceeds by metathesis steps.
+ ROMP
+ ring-opening metathesis polymerisation
+ MOP:0000685
+ ring-opening metathesis polymerisation
+
+
+
+
+ A ring-opening polymerisation that proceeds by metathesis steps.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A polymerisation in which a cyclic monomer yields a monomeric unit which is acyclic or contains fewer cycles than the monomer. If the monomer is polycyclic, the opening of a single ring is sufficient to classify the reaction as a ring-opening polymerisation.
+ ring-opening polymerization
+ MOP:0000686
+ ring-opening polymerisation
+
+
+
+
+ A polymerisation in which a cyclic monomer yields a monomeric unit which is acyclic or contains fewer cycles than the monomer. If the monomer is polycyclic, the opening of a single ring is sufficient to classify the reaction as a ring-opening polymerisation.
+ https://doi.org/10.1351/goldbook.R05396
+
+
+
+
+
+
+
+
+ A molecular process involving the exchange of a bond or bonds between similar interacting chemical species so that the bonding affiliations in the products are identical or closely similar to those in the reactants. An example is where RCH=CHR reacts with R'CH=CHR' to form 2RCH=CHR'.
+ metathesis reaction
+ MOP:0000687
+ metathesis
+
+
+
+
+ A molecular process involving the exchange of a bond or bonds between similar interacting chemical species so that the bonding affiliations in the products are identical or closely similar to those in the reactants. An example is where RCH=CHR reacts with R'CH=CHR' to form 2RCH=CHR'.
+ https://doi.org/10.1351/goldbook.M03878
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A ring-opening polymerisation where the product is a copolymer.
+ ring-opening copolymerization
+ MOP:0000688
+ ring-opening copolymerisation
+
+
+
+
+ A ring-opening polymerisation where the product is a copolymer.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A living polymerisation process where a transfer agent AX, reacts reversibly with an initiating radical R. or a propagating radical R(M)[n]. to give another transfer agent RX or R(M)[n]X and a species capable of initiating polymerisation.
+ RAFT polymerisation
+ RAFT polymerization
+ reversible addition--fragmentation chain transfer polymerization
+ reversible addition-fragmentation chain transfer polymerisation
+ reversible addition-fragmentation chain transfer polymerization
+ MOP:0000689
+ reversible addition-fragmentation chain transfer polymerisation
+
+
+
+
+ A living polymerisation process where a transfer agent AX, reacts reversibly with an initiating radical R. or a propagating radical R(M)[n]. to give another transfer agent RX or R(M)[n]X and a species capable of initiating polymerisation.
+ https://doi.org/10.1021/ma9804951
+
+
+
+
+
+
+
+
+ A living polymerisation process where the rate is controlled by a nitroxide (originally TEMPO) reacting with growing radicals to form an unreactive alkoxyamine.
+ nitroxide mediated polymerisation
+ nitroxide-mediated polymerisation
+ nitroxide-mediated polymerization
+ MOP:0000690
+ nitroxide-mediated polymerisation
+
+
+
+
+ A living polymerisation process where the rate is controlled by a nitroxide (originally TEMPO) reacting with growing radicals to form an unreactive alkoxyamine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A polymerisation process that is catalysed by an enzyme.
+ enzymatic polymerization
+ MOP:0000691
+ enzymatic polymerisation
+
+
+
+
+ A polymerisation process that is catalysed by an enzyme.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A polymerisation process that takes place in the liquid phase.
+ liquid-phase polymerization
+ MOP:0000692
+ liquid-phase polymerisation
+
+
+
+
+ A polymerisation process that takes place in the liquid phase.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A copolymerisation in which an alternating copolymer is formed.
+ alternating copolymerization
+ MOP:0000693
+ alternating copolymerisation
+
+
+
+
+ A copolymerisation in which an alternating copolymer is formed.
+ https://doi.org/10.1351/goldbook.A00251
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A copolymerisation in which a graft copolymer is formed.
+ graft copolymerization
+ MOP:0000694
+ graft copolymerisation
+
+
+
+
+ A copolymerisation in which a graft copolymer is formed.
+ https://doi.org/10.1351/goldbook.G02676
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A copolymerisation in which a periodic copolymer is formed.
+ periodic copolymerization
+ MOP:0000695
+ periodic copolymerisation
+
+
+
+
+ A copolymerisation in which a periodic copolymer is formed.
+ https://doi.org/10.1351/goldbook.P04495
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A copolymerisation in which a random copolymer is formed.
+ random copolymerization
+ MOP:0000696
+ random copolymerisation
+
+
+
+
+ A copolymerisation in which a random copolymer is formed.
+ https://doi.org/10.1351/goldbook.R05127
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A copolymerisation in which a statistical copolymer is formed.
+ statistical copolymerization
+ MOP:0000697
+ statistical copolymerisation
+
+
+
+
+ A copolymerisation in which a statistical copolymer is formed.
+ https://doi.org/10.1351/goldbook.S05956
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A copolymerisation in which a tactic copolymer is formed.
+ stereospecific copolymerization
+ MOP:0000698
+ stereospecific copolymerisation
+
+
+
+
+ A copolymerisation in which a tactic copolymer is formed.
+ https://doi.org/10.1351/goldbook.R05127
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A copolymerisation in which a block copolymer is formed.
+ block copolymerization
+ MOP:0000699
+ block copolymerisation
+
+
+
+
+ A copolymerisation in which a block copolymer is formed.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A copolymerisation in which a diblock copolymer is formed.
+ diblock copolymerization
+ MOP:0000700
+ diblock copolymerisation
+
+
+
+
+ A copolymerisation in which a diblock copolymer is formed.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A copolymerisation in which a triblock copolymer is formed.
+ triblock copolymerization
+ MOP:0000701
+ triblock copolymerisation
+
+
+
+
+ A copolymerisation in which a triblock copolymer is formed.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A polymerisation in which a graft polymer is formed.
+ graft polymerization
+ MOP:0000702
+ graft polymerisation
+
+
+
+
+ A polymerisation in which a graft polymer is formed.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A molecular process where a bond between an acetyl group and a nitrogen atom is broken.
+ MOP:0000703
+ N-deacetylation
+
+
+
+
+ A molecular process where a bond between an acetyl group and a nitrogen atom is broken.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A molecular process where a bond between an acetyl group and an oxygen atom is broken.
+ MOP:0000704
+ O-deacetylation
+
+
+
+
+ A molecular process where a bond between an acetyl group and an oxygen atom is broken.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An oxidation process where the oxidation state of at least one sulfur atom increases.
+ MOP:0000705
+ oxidation at sulfur
+
+
+
+
+ An oxidation process where the oxidation state of at least one sulfur atom increases.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An oxidation process where the oxidation state of at least one nitrogen atom increases.
+ MOP:0000706
+ oxidation at nitrogen
+
+
+
+
+ An oxidation process where the oxidation state of at least one nitrogen atom increases.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A bond-breaking process where the oxidation states of the reactive centres increase.
+ MOP:0000707
+ oxidative cleavage
+
+
+
+
+ A bond-breaking process where the oxidation states of the reactive centres increase.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ Oxidative cleavage of an alkene.
+ MOP:0000708
+ alkene oxidative cleavage
+
+
+
+
+ Oxidative cleavage of an alkene.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Oxidation of an allyl compound to an allylic alcohol.
+ MOP:0000709
+ allylic oxidation
+
+
+
+
+ Oxidation of an allyl compound to an allylic alcohol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Oxidation of an benzyl compound to an benzylic alcohol.
+ MOP:0000710
+ benzylic oxidation
+
+
+
+
+ Oxidation of an benzyl compound to an benzylic alcohol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reduction of a nitrile to the corresponding primary amine.
+ MOP:0000711
+ nitrile reduction
+
+
+
+
+ Reduction of a nitrile to the corresponding primary amine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Hydrogenation of an olefin to a paraffin.
+ MOP:0000712
+ olefin reduction
+
+
+
+
+ Hydrogenation of an olefin to a paraffin.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Hydrogenation of an acetylene to an olefin.
+ MOP:0000713
+ acetylene reduction
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A ligand exchange reaction is a molecular process, in which one or more ligands around a metal ion are replaced by other ligands without changing the oxidation state of the metal atom.
+
+ 2021-11-03T09:13:45Z
+ ligand substitution reaction
+ MOP:0000714
+ Typically, weakly bound ligands are replaced by more strongly bound ones, so that the resulting complex becomes thermodynamically more stable.
+ ligand exchange reaction
+
+
+
+
+ A ligand exchange reaction is a molecular process, in which one or more ligands around a metal ion are replaced by other ligands without changing the oxidation state of the metal atom.
+ https://doi.org/10.1093/oso/9780195301007.003.0005
+ A definition of this term in the Gold Book was not yet available at the time of addition. However, inclusion in the Gold Book was requested in October 2021.
+
+
+
+
+
+
+
+
+ The formation of a trimer from three molecular subunits.
+
+ 2022-02-01T09:40:48Z
+ MOP:0000715
+ trimerization
+
+
+
+
+ The formation of a trimer from three molecular subunits.
+ https://en.wiktionary.org/wiki/trimerization
+
+
+
+
+
+
+
+
+
+ The formation of a trimer by cycloaddition of three unsaturated compounds (e.g. alkynes, alkenes, nitriles or mixtures thereof). A metal catalyst is usually required for this type of reaction.
+
+ 2022-02-01T09:48:59Z
+ MOP:0000716
+ cyclotrimerization
+
+
+
+
+ The formation of a trimer by cycloaddition of three unsaturated compounds (e.g. alkynes, alkenes, nitriles or mixtures thereof). A metal catalyst is usually required for this type of reaction.
+ https://doi.org/10.1002/anie.200700802
+
+
+
+
+
+
+
+
+ A sigmatropic rearrangement where the intermediate consists of two three-electron fragments.
+ RXNO:0000027
+ MOP:0000721
+ This term was obsoleted from the RXNO namespace and transferred to MOP because it is a process identifiable by its mechanism rather than the intention of the experimenter.
+ [3,3]-sigmatropic rearrangement
+
+
+
+
+ A sigmatropic rearrangement where the intermediate consists of two three-electron fragments.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Isomerisation between tautomers.
+ MOP:0000724
+ tautomerisation
+
+
+
+
+ Isomerisation between tautomers.
+ https://doi.org/10.1351/goldbook.T06252
+
+
+
+
+
+
+
+
+ Isomerisation between the keto- and enol-forms of a molecule.
+ MOP:0000725
+ keto-enol tautomerisation
+
+
+
+
+ Isomerisation between the keto- and enol-forms of a molecule.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Tautomerisation that involves the breaking of a ring in one direction and formation of a ring in the other.
+ MOP:0000726
+ ring-chain tautomerisation
+
+
+
+
+ Tautomerisation that involves the breaking of a ring in one direction and formation of a ring in the other.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A tautomerisation process where the leaving group is a proton.
+ MOP:0000727
+ prototropy
+
+
+
+
+ A tautomerisation process where the leaving group is a proton.
+ https://doi.org/10.1351/goldbook.T06252
+
+
+
+
+
+
+
+
+ A molecular process that involves breaking a sigma bond, creating a sigma bond between two unconnected atoms and preserving the number of pi bonds in the system.
+ MOP:0000728
+ sigmatropic rearrangement
+
+
+
+
+ A molecular process that involves breaking a sigma bond, creating a sigma bond between two unconnected atoms and preserving the number of pi bonds in the system.
+ https://doi.org/10.1351/goldbook.S05660
+
+
+
+
+
+
+
+
+ A reversible molecular process that involves the breaking or formation of single or double bonds without migrating atoms or groups.
+ MOP:0000729
+ valence tautomerisation
+
+
+
+
+ A reversible molecular process that involves the breaking or formation of single or double bonds without migrating atoms or groups.
+ https://doi.org/10.1351/goldbook.V06591
+
+
+
+
+
+
+
+
+ Catalysis where the catalyst is a Brønsted acid.
+ batchelorc
+ 2014-04-09T10:00:00Z
+ MOP:0000730
+ Brønsted acid catalysis
+
+
+
+
+ Catalysis where the catalyst is a Brønsted acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Catalysis where the catalyst is a base.
+ batchelorc
+ 2014-04-09T10:00:00Z
+ MOP:0000731
+ base catalysis
+
+
+
+
+ Catalysis where the catalyst is a base.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A molecular process where a Brønsted acid donates a hydron to a Brønsted base.
+ batchelorc
+ 2014-04-09T10:00:00Z
+ MOP:0000732
+ hydron donation
+
+
+
+
+ A molecular process where a Brønsted acid donates a hydron to a Brønsted base.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A molecular process where a Lewis acid accepts an electron pair from a Lewis base.
+ batchelorc
+ 2014-04-09T10:00:00Z
+ MOP:0000733
+ accepting an electron pair in Lewis adduct formation
+
+
+
+
+ A molecular process where a Lewis acid accepts an electron pair from a Lewis base.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Catalysis where the catalyst is a Lewis acid.
+ batchelorc
+ 2014-04-09T10:00:00Z
+ MOP:0000734
+ Lewis acid catalysis
+
+
+
+
+ Catalysis where the catalyst is a Lewis acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Catalysis where the catalyst is a Lewis base.
+ batchelorc
+ 2014-04-09T10:00:00Z
+ MOP:0000735
+ Lewis base catalysis
+
+
+
+
+ Catalysis where the catalyst is a Lewis base.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Catalysis where the catalyst is a Brønsted base.
+ batchelorc
+ 2014-04-09T10:00:00Z
+ MOP:0000736
+ Brønsted base catalysis
+
+
+
+
+ Catalysis where the catalyst is a Brønsted base.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A molecular process where a Brønsted base accepts a hydron from a Brønsted acid.
+ batchelorc
+ 2014-04-09T10:00:00Z
+ MOP:0000737
+ accepting a hydron
+
+
+
+
+ A molecular process where a Brønsted base accepts a hydron from a Brønsted acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A molecular process where a Lewis base donates an electron pair to a Lewis acid.
+ batchelorc
+ 2014-04-09T10:00:00Z
+ MOP:0000738
+ electron pair donation in Lewis adduct formation
+
+
+
+
+ A molecular process where a Lewis base donates an electron pair to a Lewis acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A molecular process where a Lewis adduct is formed from a Lewis acid and a Lewis base.
+ MOP:0000739
+ Lewis adduct formation
+
+
+
+
+ A molecular process where a Lewis adduct is formed from a Lewis acid and a Lewis base.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Catalysis of a reaction where the catalyst either donates a hydron or accepts an electron pair.
+ MOP:0000740
+ acid catalysis
+
+
+
+
+ Catalysis of a reaction where the catalyst either donates a hydron or accepts an electron pair.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An exocyclization where a four-membered ring is formed with bond formation at a tetragonal centre.
+ 4-exo-tet cyclisation
+ MOP:0000741
+ 4-exo-tet cyclization
+
+
+
+
+ An exocyclization where a four-membered ring is formed with bond formation at a tetragonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An exocyclization where a five-membered ring is formed with bond formation at a tetragonal centre.
+ 5-exo-tet cyclisation
+ MOP:0000742
+ 5-exo-tet cyclization
+
+
+
+
+ An exocyclization where a five-membered ring is formed with bond formation at a tetragonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An exocyclization where a six-membered ring is formed with bond formation at a tetragonal centre.
+ 6-exo-tet cyclisation
+ MOP:0000743
+ 6-exo-tet cyclization
+
+
+
+
+ An exocyclization where a six-membered ring is formed with bond formation at a tetragonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An exocyclization where a seven-membered ring is formed with bond formation at a tetragonal centre.
+ 7-exo-tet cyclisation
+ MOP:0000744
+ 7-exo-tet cyclization
+
+
+
+
+ An exocyclization where a seven-membered ring is formed with bond formation at a tetragonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An endocyclization where a five-membered ring is formed with bond formation at a tetragonal centre.
+ 5-endo-tet cyclisation
+ MOP:0000745
+ 5-endo-tet cyclization
+
+
+
+
+ An endocyclization where a five-membered ring is formed with bond formation at a tetragonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An endocyclization where a six-membered ring is formed with bond formation at a tetragonal centre.
+ 6-endo-tet cyclisation
+ MOP:0000746
+ 6-endo-tet cyclization
+
+
+
+
+ An endocyclization where a six-membered ring is formed with bond formation at a tetragonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An endocyclization where a seven-membered ring is formed with bond formation at a tetragonal centre.
+ 7-endo-tet cyclisation
+ MOP:0000747
+ 7-endo-tet cyclization
+
+
+
+
+ An endocyclization where a seven-membered ring is formed with bond formation at a tetragonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An exocyclization where a three-membered ring is formed with bond formation at a trigonal centre.
+ 3-exo-trig cyclisation
+ MOP:0000748
+ 3-exo-trig cyclization
+
+
+
+
+ An exocyclization where a three-membered ring is formed with bond formation at a trigonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An exocyclization where a three-membered ring is formed with bond formation at a digonal centre.
+ 3-exo-dig cyclisation
+ MOP:0000749
+ 3-exo-dig cyclization
+
+
+
+
+ An exocyclization where a three-membered ring is formed with bond formation at a digonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An endocyclization where a three-membered ring is formed with bond formation at a digonal centre.
+ 3-endo-dig cyclisation
+ MOP:0000750
+ 3-endo-dig cyclization
+
+
+
+
+ An endocyclization where a three-membered ring is formed with bond formation at a digonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An endocyclization where a three-membered ring is formed with bond formation at a trigonal centre.
+ 3-endo-trig cyclisation
+ MOP:0000751
+ 3-endo-trig cyclization
+
+
+
+
+ An endocyclization where a three-membered ring is formed with bond formation at a trigonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An exocyclization where a four-membered ring is formed with bond formation at a trigonal centre.
+ 4-exo-trig cyclisation
+ MOP:0000752
+ 4-exo-trig cyclization
+
+
+
+
+ An exocyclization where a four-membered ring is formed with bond formation at a trigonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An endocyclization where a four-membered ring is formed with bond formation at a trigonal centre.
+ 4-endo-trig cyclisation
+ MOP:0000753
+ 4-endo-trig cyclization
+
+
+
+
+ An endocyclization where a four-membered ring is formed with bond formation at a trigonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An endocyclization where a four-membered ring is formed with bond formation at a digonal centre.
+ 4-endo-dig cyclisation
+ MOP:0000754
+ 4-endo-dig cyclization
+
+
+
+
+ An endocyclization where a four-membered ring is formed with bond formation at a digonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An exocyclization where a five-membered ring is formed with bond formation at a trigonal centre.
+ 5-exo-trig cyclisation
+ MOP:0000755
+ 5-exo-trig cyclization
+
+
+
+
+ An exocyclization where a five-membered ring is formed with bond formation at a trigonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An exocyclization where a five-membered ring is formed with bond formation at a digonal centre.
+ 5-exo-dig cyclisation
+ MOP:0000756
+ 5-exo-dig cyclization
+
+
+
+
+ An exocyclization where a five-membered ring is formed with bond formation at a digonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An endocyclization where a five-membered ring is formed with bond formation at a trigonal centre.
+ 5-endo-trig cyclisation
+ MOP:0000757
+ 5-endo-trig cyclization
+
+
+
+
+ An endocyclization where a five-membered ring is formed with bond formation at a trigonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An endocyclization where a five-membered ring is formed with bond formation at a digonal centre.
+ 5-endo-dig cyclisation
+ MOP:0000758
+ 5-endo-dig cyclization
+
+
+
+
+ An endocyclization where a five-membered ring is formed with bond formation at a digonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An endocyclization where a six-membered ring is formed with bond formation at a trigonal centre.
+ 6-endo-trig cyclisation
+ MOP:0000759
+ 6-endo-trig cyclization
+
+
+
+
+ An endocyclization where a six-membered ring is formed with bond formation at a trigonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An endocyclization where a seven-membered ring is formed with bond formation at a trigonal centre.
+ 7-endo-trig cyclisation
+ MOP:0000760
+ 7-endo-trig cyclization
+
+
+
+
+ An endocyclization where a seven-membered ring is formed with bond formation at a trigonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An endocyclization where a seven-membered ring is formed with bond formation at a digonal centre.
+ 7-endo-dig cyclisation
+ MOP:0000761
+ 7-endo-dig cyclization
+
+
+
+
+ An endocyclization where a seven-membered ring is formed with bond formation at a digonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An exocyclization where a four-membered ring is formed with bond formation at a digonal centre.
+ 4-exo-dig cyclisation
+ MOP:0000762
+ 4-exo-dig cyclization
+
+
+
+
+ An exocyclization where a four-membered ring is formed with bond formation at a digonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An exocyclization where a six-membered ring is formed with bond formation at a digonal centre.
+ 6-exo-dig cyclisation
+ MOP:0000763
+ 6-exo-dig cyclization
+
+
+
+
+ An exocyclization where a six-membered ring is formed with bond formation at a digonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An exocyclization where a seven-membered ring is formed with bond formation at a digonal centre.
+ 7-exo-dig cyclisation
+ MOP:0000764
+ 7-exo-dig cyclization
+
+
+
+
+ An exocyclization where a seven-membered ring is formed with bond formation at a digonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An exocyclization where a six-membered ring is formed with bond formation at a trigonal centre.
+ 6-exo-trig cyclisation
+ MOP:0000765
+ 6-exo-trig cyclization
+
+
+
+
+ An exocyclization where a six-membered ring is formed with bond formation at a trigonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An exocyclization where a seven-membered ring is formed with bond formation at a trigonal centre.
+ 7-exo-trig cyclisation
+ MOP:0000766
+ 7-exo-trig cyclization
+
+
+
+
+ An exocyclization where a seven-membered ring is formed with bond formation at a trigonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A reaction for which the overall standard enthalpy change is positive.
+ REX:0000368
+ MOP:0000767
+ endothermic reaction
+
+
+
+
+ A reaction for which the overall standard enthalpy change is positive.
+ https://doi.org/10.1351/goldbook.E02095
+
+
+
+
+
+
+
+
+ A reaction for which the overall standard enthalpy change is negative.
+ REX:0000369
+ MOP:0000768
+ exothermic reaction
+
+
+
+
+ A reaction for which the overall standard enthalpy change is negative.
+ https://doi.org/10.1351/goldbook.E02269
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An endocyclization where a six-membered ring is formed with bond formation at a digonal centre.
+ 6-endo-dig cyclisation
+ MOP:0000770
+ 6-endo-dig cyclization
+
+
+
+
+ An endocyclization where a six-membered ring is formed with bond formation at a digonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A cyclization where there is a reduction in bond order of a bond that ends up within the newly-formed ring.
+ endocyclisation
+ MOP:0000771
+ endocyclization
+
+
+
+
+ A cyclization where there is a reduction in bond order of a bond that ends up within the newly-formed ring.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A cyclization where there is a reduction in bond order of a bond that ends up outside the newly-formed ring.
+ exocyclisation
+ MOP:0000772
+ exocyclization
+
+
+
+
+ A cyclization where there is a reduction in bond order of a bond that ends up outside the newly-formed ring.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Profile of a cyclization that is favoured according to Baldwin's empirical rules. These apply best to neutral systems consisting of first-row atoms.
+ MOP:0000773
+ Baldwin-favoured profile
+
+
+
+
+ Profile of a cyclization that is favoured according to Baldwin's empirical rules. These apply best to neutral systems consisting of first-row atoms.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Profile of a cyclization that is disfavoured according to Baldwin's empirical rules. These apply best to neutral systems consisting of first-row atoms.
+ MOP:0000774
+ Baldwin-disfavoured profile
+
+
+
+
+ Profile of a cyclization that is disfavoured according to Baldwin's empirical rules. These apply best to neutral systems consisting of first-row atoms.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A covalent bond formation where the active centre has sp hybridization.
+ MOP:0000775
+ bond formation to digonal centre
+
+
+
+
+ A covalent bond formation where the active centre has sp hybridization.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A bond formation where the active centre has sp2 hybridization.
+ MOP:0000776
+ bond formation to trigonal centre
+
+
+
+
+ A bond formation where the active centre has sp2 hybridization.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A bond formation where the active centre has sp3 hybridization.
+ MOP:0000777
+ bond formation to tetragonal centre
+
+
+
+
+ A bond formation where the active centre has sp3 hybridization.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An exocyclization where a three-membered ring is formed with bond formation at a tetragonal centre.
+ 3-exo-tet cyclisation
+ MOP:0000778
+ 3-exo-tet cyclization
+
+
+
+
+ An exocyclization where a three-membered ring is formed with bond formation at a tetragonal centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A molecular process in which a covalent bond is formed.
+ MOP:0000779
+ formation of covalent bond
+
+
+
+
+ A molecular process in which a covalent bond is formed.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A molecular process in which a covalent bond is broken.
+ MOP:0000780
+ breaking of covalent bond
+
+
+
+
+ A molecular process in which a covalent bond is broken.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A molecular process resulting in the rate of another molecular process being increased without modifying the other process's overall Gibbs standard energy change.
+ MOP:0000781
+ catalysis
+
+
+
+
+ A molecular process resulting in the rate of another molecular process being increased without modifying the other process's overall Gibbs standard energy change.
+ https://doi.org//10.1351/goldbook.C00876
+
+
+
+
+
+
+
+
+ A Brønsted acid catalysis where all species that can contribute protons contribute to the increase in reaction rate.
+ batchelorc
+ 2014-09-02T13:15:00Z
+ MOP:0000782
+ general acid catalysis
+
+
+
+
+ A Brønsted acid catalysis where all species that can contribute protons contribute to the increase in reaction rate.
+ https://doi.org//10.1359/goldbook.G02609
+
+
+
+
+
+
+
+
+ A Brønsted acid catalysis where the reaction rate is proportional to the concentration of protonated solvent molecules.
+ batchelorc
+ 2014-09-02T13:15:00Z
+ MOP:0000783
+ specific acid catalysis
+
+
+
+
+ A Brønsted acid catalysis where the reaction rate is proportional to the concentration of protonated solvent molecules.
+ https://doi.org//10.1359/goldbook.S05796
+
+
+
+
+
+
+
+
+ A Brønsted base catalysis where the reaction rate is proportional to the concentration of hydroxide ions.
+ batchelorc
+ 2014-09-02T13:15:00Z
+ MOP:0000784
+ general base catalysis
+
+
+
+
+ A Brønsted base catalysis where the reaction rate is proportional to the concentration of hydroxide ions.
+ https://doi.org//10.1359/goldbook.G02610
+
+
+
+
+
+
+
+
+ A Brønsted base catalysis where the reaction rate is proportional to the concentration of hydron acceptors.
+ batchelorc
+ 2014-09-02T13:15:00Z
+ MOP:0000785
+ specific base catalysis
+
+
+
+
+ A Brønsted base catalysis where the reaction rate is proportional to the concentration of hydron acceptors.
+ https://doi.org//10.1359/goldbook.S05796
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A molecular process in which a molecular entity possessing an unpaired electron is formed.
+ MOP:0000786
+ radical formation
+
+
+
+
+ A molecular process in which a molecular entity possessing an unpaired electron is formed.
+ RSC:xp
+
+
+
+
+
+
+
+
+ An alcoholysis reaction of an ester which produces a different alcohol and a different ester.
+ MOP:0000787
+ transesterification
+
+
+
+
+ An alcoholysis reaction of an ester which produces a different alcohol and a different ester.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A covalent-bond-breaking reaction where the attacking group is a phosphate ion.
+ MOP:0000788
+ phosphorolysis
+
+
+
+
+ A covalent-bond-breaking reaction where the attacking group is a phosphate ion.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A molecular process where the product is an isomer of the reactant.
+ MOP:0000789
+ isomerisation
+
+
+
+
+ A molecular process where the product is an isomer of the reactant.
+ https://doi.org/10.1359/goldbook.I03295
+
+
+
+
+
+
+
+
+ A reaction in which one singly-bonded group, but not the hydrogen atom, is replaced by another singly-bonded group.
+ RXNO:0000019
+ MOP:0000790
+ The Gold Book says hydrogen atoms count, but this differs from everyone's intuition. See http://goldbook.iupac.org/S06078.html
+ substitution reaction
+
+
+
+
+ A reaction in which one singly-bonded group, but not the hydrogen atom, is replaced by another singly-bonded group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A substitution reaction in which one singly-bonded substituent on an aromatic skeleton is replaced by another singly-bonded substituent.
+ RXNO:0000020
+ MOP:0000791
+ aromatic substitution
+
+
+
+
+ A substitution reaction in which one singly-bonded substituent on an aromatic skeleton is replaced by another singly-bonded substituent.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A substitution reaction in an allylic system with concomitant migration of the allyl double bond.
+ RXNO:0000033
+ MOP:0000792
+ allylic rearrangement
+
+
+
+
+ A substitution reaction in an allylic system with concomitant migration of the allyl double bond.
+ RSC:cc
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A substitution reaction where the reactive centre is a nitrogen atom.
+ RXNO:0000319
+ MOP:0000793
+ N-substitution
+
+
+
+
+ A substitution reaction where the reactive centre is a nitrogen atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A substitution reaction where the reactive centre is an oxygen atom.
+ RXNO:0000318
+ NAMERXN:1.7
+ MOP:0000794
+ O-substitution
+
+
+
+
+ A substitution reaction where the reactive centre is an oxygen atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A substitution reaction where the reactive centre is a sulfur atom.
+ batchelorc
+ 2012-03-22T12:22:59Z
+ RXNO:0000336
+ NAMERXN:1.8
+ MOP:0000795
+ S-substitution
+
+
+
+
+ A substitution reaction where the reactive centre is a sulfur atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An aromatic substitution reaction where a chloro substituent is replaced by a hydroxy substituent.
+ MOP:0000796
+ chloro- to hydroxy- aromatic substitution
+
+
+
+
+ An aromatic substitution reaction where a chloro substituent is replaced by a hydroxy substituent.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond where the two shared electrons have come from only one of the reactants.
+ MOP:0000797
+ coordination
+
+
+
+
+ Formation of a covalent bond where the two shared electrons have come from only one of the reactants.
+ https://doi.org/10.1351/goldbook.C01329
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a sulfur centre.
+ MOP:0000798
+ formation of covalent bond with sulfur centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a sulfur centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a chlorine centre.
+ MOP:0000799
+ formation of covalent bond with chlorine centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a chlorine centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a carbon centre.
+ MOP:0000800
+ formation of covalent bond with carbon centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a carbon centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a boron centre.
+ MOP:0000801
+ formation of covalent bond with boron centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a boron centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a nitrogen centre.
+ MOP:0000802
+ formation of covalent bond with nitrogen centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a nitrogen centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a oxygen centre.
+ MOP:0000803
+ formation of covalent bond with oxygen centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a oxygen centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a selenium centre.
+ MOP:0000804
+ formation of covalent bond with selenium centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a selenium centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a tellurium centre.
+ MOP:0000805
+ formation of covalent bond with tellurium centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a tellurium centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a phosphorus centre.
+ MOP:0000806
+ formation of covalent bond with phosphorus centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a phosphorus centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a arsenic centre.
+ MOP:0000807
+ formation of covalent bond with arsenic centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a arsenic centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a antimony centre.
+ MOP:0000808
+ formation of covalent bond with antimony centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a antimony centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a germanium centre.
+ MOP:0000809
+ formation of covalent bond with germanium centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a germanium centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a silicon centre.
+ MOP:0000810
+ formation of covalent bond with silicon centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a silicon centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on an aluminium centre.
+ MOP:0000811
+ formation of covalent bond with aluminium centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on an aluminium centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a tin centre.
+ MOP:0000812
+ formation of covalent bond with tin centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a tin centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a lead centre.
+ MOP:0000813
+ formation of covalent bond with lead centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a lead centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a gallium centre.
+ MOP:0000814
+ formation of covalent bond with gallium centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a gallium centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on an indium centre.
+ MOP:0000815
+ formation of covalent bond with indium centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on an indium centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a thallium centre.
+ MOP:0000816
+ formation of covalent bond with thallium centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a thallium centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a bromine centre.
+ MOP:0000817
+ formation of covalent bond with bromine centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a bromine centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on an iodine centre.
+ MOP:0000818
+ formation of covalent bond with iodine centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on an iodine centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a fluorine centre.
+ MOP:0000819
+ formation of covalent bond with fluorine centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a fluorine centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a halogen centre.
+ MOP:0000820
+ formation of covalent bond with halogen centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a halogen centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a metal atom and a nitrosyl group.
+ MOP:0000821
+ metal nitrosylation
+
+
+
+
+ Formation of a covalent bond between a metal atom and a nitrosyl group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an iron atom and a nitrosyl group.
+ MOP:0000822
+ iron nitrosylation
+
+
+
+
+ Formation of a covalent bond between an iron atom and a nitrosyl group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a propargyl group.
+ MOP:0000823
+ propargylation
+
+
+
+
+ Formation of a covalent bond with a propargyl group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with an alkynyl group.
+ MOP:0000824
+ alkynylation
+
+
+
+
+ Formation of a covalent bond with an alkynyl group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a boryl group (-BR'R').
+ MOP:0001000
+ Submitted to ChEBI
+ deborylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a boryl group (-BR'R').
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a methanidyl group.
+ MOP:0001001
+ has_participant: CHEBI:29361
+ demethanidylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a methanidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an azaniumyl group.
+ MOP:0001002
+ has_participant: CHEBI:48284
+ deazaniumylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an azaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a formyl group.
+ MOP:0001003
+ has_participant: CHEBI:42485
+ deformylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a formyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acetonyl group.
+ MOP:0001004
+ has_participant: CHEBI:48056
+ deacetonylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acetonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-cystyl group.
+ MOP:0001005
+ has_participant: CHEBI:50057
+ de-L-cystylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-cystinyl group.
+ MOP:0001006
+ has_participant: CHEBI:50066
+ de-L-cystinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-cystinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-cystyl group.
+ MOP:0001007
+ has_participant: CHEBI:50049
+ de-D-cystylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cystinyl group.
+ MOP:0001008
+ has_participant: CHEBI:50050
+ decystinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cystinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cystyl group.
+ MOP:0001009
+ has_participant: CHEBI:23514
+ decystylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cysteinyl group.
+ MOP:0001010
+ has_participant: CHEBI:23511
+ decysteinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-cysteinyl group.
+ MOP:0001011
+ has_participant: CHEBI:32447
+ de-L-cysteinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-cysteinyl group.
+ MOP:0001012
+ has_participant: CHEBI:32452
+ de-D-cysteinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cystein-S-yl group.
+ MOP:0001013
+ has_participant: CHEBI:32795
+ decystein-S-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-cystein-S-yl group.
+ MOP:0001014
+ has_participant: CHEBI:32794
+ de-D-cystein-S-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-cystein-S-yl group.
+ MOP:0001015
+ has_participant: CHEBI:32793
+ de-L-cystein-S-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a methionyl group.
+ MOP:0001016
+ has_participant: CHEBI:37902
+ demethionylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-methionyl group.
+ MOP:0001017
+ has_participant: CHEBI:49038
+ de-L-methionylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-formyl-L-methionyl group.
+ MOP:0001018
+ has_participant: CHEBI:49298
+ de-N-formyl-L-methionylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-formyl-L-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-methionyl group.
+ MOP:0001019
+ has_participant: CHEBI:32640
+ de-D-methionylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an (R)-lipoyl group.
+ MOP:0001020
+ has_participant: CHEBI:38232
+ de-(R)-lipoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an (R)-lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an (S)-lipoyl group.
+ MOP:0001021
+ has_participant: CHEBI:38233
+ de-(S)-lipoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an (S)-lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a lipoyl group.
+ MOP:0001022
+ has_participant: CHEBI:25064
+ delipoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an (R)-dihydrolipoyl group.
+ MOP:0001023
+ has_participant: CHEBI:30319
+ de-(R)-dihydrolipoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an (R)-dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an (S)-dihydrolipoyl group.
+ MOP:0001024
+ has_participant: CHEBI:50489
+ de-(S)-dihydrolipoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an (S)-dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-sialoyl group.
+ MOP:0001025
+ has_participant: CHEBI:32960
+ de-alpha-sialoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-sialoyl group.
+ MOP:0001026
+ has_participant: CHEBI:32961
+ de-beta-sialoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glyceroyl group.
+ MOP:0001027
+ has_participant: CHEBI:30750
+ deglyceroylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glyceroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carboacyl group.
+ MOP:0001028
+ has_participant: CHEBI:37838
+ decarboacylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an univalent carboacyl group.
+ MOP:0001029
+ has_participant: CHEBI:27207
+ deunivalent carboacylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an univalent carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acetyl group.
+ MOP:0001030
+ has_participant: CHEBI:40574
+ deacetylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-aminoacyl group.
+ MOP:0001031
+ has_participant: CHEBI:22487
+ de-alpha-aminoacylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-aminoacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alanyl group.
+ MOP:0001032
+ has_participant: CHEBI:22280
+ dealanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-alanyl group.
+ MOP:0001033
+ has_participant: CHEBI:32433
+ de-L-alanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-alanyl group.
+ MOP:0001034
+ has_participant: CHEBI:32437
+ de-D-alanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-aspartyl group.
+ MOP:0001035
+ has_participant: CHEBI:22445
+ de-alpha-aspartylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-alpha-aspartyl group.
+ MOP:0001036
+ has_participant: CHEBI:32462
+ de-L-alpha-aspartylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-alpha-aspartyl group.
+ MOP:0001037
+ has_participant: CHEBI:32466
+ de-D-alpha-aspartylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-glutamyl group.
+ MOP:0001038
+ has_participant: CHEBI:22453
+ de-alpha-glutamylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-alpha-glutamyl group.
+ MOP:0001039
+ has_participant: CHEBI:46855
+ de-L-alpha-glutamylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-alpha-glutamyl group.
+ MOP:0001040
+ has_participant: CHEBI:32479
+ de-D-alpha-glutamylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pteroylglutamyl group.
+ MOP:0001041
+ has_participant: CHEBI:26380
+ depteroylglutamylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pteroylglutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phenylalanyl group.
+ MOP:0001042
+ has_participant: CHEBI:25987
+ dephenylalanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-phenylalanyl group.
+ MOP:0001043
+ has_participant: CHEBI:32496
+ de-L-phenylalanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-phenylalanyl group.
+ MOP:0001044
+ has_participant: CHEBI:32500
+ de-D-phenylalanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glycyl group.
+ MOP:0001045
+ has_participant: CHEBI:46740
+ deglycylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glycyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a histidyl group.
+ MOP:0001046
+ has_participant: CHEBI:37906
+ dehistidylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-histidyl group.
+ MOP:0001047
+ has_participant: CHEBI:32514
+ de-L-histidylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-histidyl group.
+ MOP:0001048
+ has_participant: CHEBI:32522
+ de-D-histidylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an isoleucyl group.
+ MOP:0001049
+ has_participant: CHEBI:37905
+ deisoleucylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-isoleucyl group.
+ MOP:0001050
+ has_participant: CHEBI:32606
+ de-L-isoleucylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-isoleucyl group.
+ MOP:0001051
+ has_participant: CHEBI:32610
+ de-D-isoleucylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a lysyl group.
+ MOP:0001052
+ has_participant: CHEBI:37903
+ delysylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-lysyl group.
+ MOP:0001053
+ has_participant: CHEBI:32553
+ de-L-lysylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a deoxyhypusinyl group.
+ MOP:0001054
+ has_participant: CHEBI:50039
+ dedeoxyhypusinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a deoxyhypusinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-lysyl group.
+ MOP:0001055
+ has_participant: CHEBI:32559
+ de-D-lysylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a leucyl group.
+ MOP:0001056
+ has_participant: CHEBI:37904
+ deleucylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-leucyl group.
+ MOP:0001057
+ has_participant: CHEBI:32621
+ de-L-leucylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-leucyl group.
+ MOP:0001058
+ has_participant: CHEBI:32625
+ de-D-leucylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an asparaginyl group.
+ MOP:0001059
+ has_participant: CHEBI:22656
+ deasparaginylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-asparaginyl group.
+ MOP:0001060
+ has_participant: CHEBI:50348
+ de-L-asparaginylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-asparaginyl group.
+ MOP:0001061
+ has_participant: CHEBI:32653
+ de-D-asparaginylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a prolyl group.
+ MOP:0001062
+ has_participant: CHEBI:26274
+ deprolylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-prolyl group.
+ MOP:0001063
+ has_participant: CHEBI:32865
+ de-L-prolylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-prolyl group.
+ MOP:0001064
+ has_participant: CHEBI:32869
+ de-D-prolylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glutaminyl group.
+ MOP:0001065
+ has_participant: CHEBI:24320
+ deglutaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-glutaminyl group.
+ MOP:0001066
+ has_participant: CHEBI:32667
+ de-L-glutaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-glutaminyl group.
+ MOP:0001067
+ has_participant: CHEBI:32674
+ de-D-glutaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a seryl group.
+ MOP:0001068
+ has_participant: CHEBI:37901
+ deserylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-seryl group.
+ MOP:0001069
+ has_participant: CHEBI:32838
+ de-L-serylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-seryl group.
+ MOP:0001070
+ has_participant: CHEBI:32842
+ de-D-serylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a threonyl group.
+ MOP:0001071
+ has_participant: CHEBI:37900
+ dethreonylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-threonyl group.
+ MOP:0001072
+ has_participant: CHEBI:32823
+ de-L-threonylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-threonyl group.
+ MOP:0001073
+ has_participant: CHEBI:32829
+ de-D-threonylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a selenocysteinyl group.
+ MOP:0001074
+ has_participant: CHEBI:32755
+ deselenocysteinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-selenocysteinyl group.
+ MOP:0001075
+ has_participant: CHEBI:32745
+ de-L-selenocysteinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-selenocysteinyl group.
+ MOP:0001076
+ has_participant: CHEBI:32749
+ de-D-selenocysteinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a valyl group.
+ MOP:0001077
+ has_participant: CHEBI:37897
+ devalylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-valyl group.
+ MOP:0001078
+ has_participant: CHEBI:32853
+ de-L-valylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-valyl group.
+ MOP:0001079
+ has_participant: CHEBI:32857
+ de-D-valylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tryptophyl group.
+ MOP:0001080
+ has_participant: CHEBI:37899
+ detryptophylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-tryptophyl group.
+ MOP:0001081
+ has_participant: CHEBI:32706
+ de-L-tryptophylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-tryptophyl group.
+ MOP:0001082
+ has_participant: CHEBI:32718
+ de-D-tryptophylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tyrosyl group.
+ MOP:0001083
+ has_participant: CHEBI:37898
+ detyrosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-tyrosyl group.
+ MOP:0001084
+ has_participant: CHEBI:32764
+ de-L-tyrosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-tyrosyl group.
+ MOP:0001085
+ has_participant: CHEBI:32778
+ de-D-tyrosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arginyl group.
+ MOP:0001086
+ has_participant: CHEBI:22619
+ dearginylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-arginyl group.
+ MOP:0001087
+ has_participant: CHEBI:32684
+ de-L-arginylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-arginyl group.
+ MOP:0001088
+ has_participant: CHEBI:32691
+ de-D-arginylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a benzoyl group.
+ MOP:0001089
+ has_participant: CHEBI:22733
+ debenzoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a benzoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-aspartyl group.
+ MOP:0001090
+ has_participant: CHEBI:22832
+ de-beta-aspartylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-beta-aspartyl group.
+ MOP:0001091
+ has_participant: CHEBI:32467
+ de-D-beta-aspartylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-beta-aspartyl group.
+ MOP:0001092
+ has_participant: CHEBI:48098
+ de-L-beta-aspartylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a biotinyl group.
+ MOP:0001093
+ has_participant: CHEBI:22885
+ debiotinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a biotinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a butyryl group.
+ MOP:0001094
+ has_participant: CHEBI:22972
+ debutyrylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a butyryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carbamoyl group.
+ MOP:0001095
+ has_participant: CHEBI:23004
+ decarbamoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carbamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a C-aminocarbonohydrazonoyl group.
+ MOP:0001096
+ has_participant: CHEBI:48223
+ de-C-aminocarbonohydrazonoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a C-aminocarbonohydrazonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-(aminomethylidene)hydrazinyl group.
+ MOP:0001097
+ has_participant: CHEBI:48244
+ de-2-(aminomethylidene)hydrazinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-(aminomethylidene)hydrazinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carbamoylcarbamoyl group.
+ MOP:0001098
+ has_participant: CHEBI:48083
+ decarbamoylcarbamoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carbamoylcarbamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carbamothioyl group.
+ MOP:0001099
+ has_participant: CHEBI:48225
+ decarbamothioylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carbamothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acetylazanediyl group.
+ MOP:0001100
+ has_participant: CHEBI:48073
+ deacetylazanediylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acetylazanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an oxamoyl group.
+ MOP:0001101
+ has_participant: CHEBI:48246
+ deoxamoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an oxamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cholyl group.
+ MOP:0001102
+ has_participant: CHEBI:23220
+ decholylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cholyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an enoyl group.
+ MOP:0001103
+ has_participant: CHEBI:23916
+ deenoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a fatty-acyl group.
+ MOP:0001104
+ has_participant: CHEBI:24027
+ defatty-acylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a fatty-acyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arachidonoyl group.
+ MOP:0001105
+ has_participant: CHEBI:22610
+ dearachidonoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arachidonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arachidoyl group.
+ MOP:0001106
+ has_participant: CHEBI:22614
+ dearachidoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arachidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a behenoyl group.
+ MOP:0001107
+ has_participant: CHEBI:22696
+ debehenoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a behenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cerotoyl group.
+ MOP:0001108
+ has_participant: CHEBI:23080
+ decerotoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cerotoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a decanoyl group.
+ MOP:0001109
+ has_participant: CHEBI:23574
+ dedecanoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a decanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a dodecenoyl group.
+ MOP:0001110
+ has_participant: CHEBI:23868
+ dedodecenoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a dodecenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an eleostearoyl group.
+ MOP:0001111
+ has_participant: CHEBI:23908
+ deeleostearoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an eleostearoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a mycolyl group.
+ MOP:0001112
+ has_participant: CHEBI:25439
+ demycolylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a mycolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nervonoyl group.
+ MOP:0001113
+ has_participant: CHEBI:25503
+ denervonoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nervonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an octanoyl group.
+ MOP:0001114
+ has_participant: CHEBI:25650
+ deoctanoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an octanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a palmitoleoyl group.
+ MOP:0001115
+ has_participant: CHEBI:25837
+ depalmitoleoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a palmitoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a palmitoyl group.
+ MOP:0001116
+ has_participant: CHEBI:45021
+ depalmitoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a palmitoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a stearoyl group.
+ MOP:0001117
+ has_participant: CHEBI:26753
+ destearoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a stearoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an undecanoyl group.
+ MOP:0001118
+ has_participant: CHEBI:27190
+ deundecanoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an undecanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a valeryl group.
+ MOP:0001119
+ has_participant: CHEBI:27265
+ devalerylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a valeryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a hexanoyl group.
+ MOP:0001120
+ has_participant: CHEBI:24574
+ dehexanoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a hexanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a heptanoyl group.
+ MOP:0001121
+ has_participant: CHEBI:32363
+ deheptanoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a heptanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nonanoyl group.
+ MOP:0001122
+ has_participant: CHEBI:25580
+ denonanoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nonanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a lauroyl group.
+ MOP:0001123
+ has_participant: CHEBI:32359
+ delauroylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a lauroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a myristoyl group.
+ MOP:0001124
+ has_participant: CHEBI:25456
+ demyristoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a myristoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a docosenoyl group.
+ MOP:0001125
+ has_participant: CHEBI:50479
+ dedocosenoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a docosenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cetoleoyl group.
+ MOP:0001126
+ has_participant: CHEBI:32430
+ decetoleoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cetoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an erucoyl group.
+ MOP:0001127
+ has_participant: CHEBI:32394
+ deerucoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an erucoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an icosenoyl group.
+ MOP:0001128
+ has_participant: CHEBI:50480
+ deicosenoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an icosenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a gadelaidoyl group.
+ MOP:0001129
+ has_participant: CHEBI:32424
+ degadelaidoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a gadelaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a gadoleoyl group.
+ MOP:0001130
+ has_participant: CHEBI:32421
+ degadoleoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a gadoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a gondoyl group.
+ MOP:0001131
+ has_participant: CHEBI:32427
+ degondoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a gondoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a heptatrienoyl group.
+ MOP:0001132
+ has_participant: CHEBI:50486
+ deheptatrienoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a heptatrienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trans,trans-hepta-2,4,6-trienoyl group.
+ MOP:0001133
+ has_participant: CHEBI:30771
+ de-trans,trans-hepta-2,4,6-trienoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trans,trans-hepta-2,4,6-trienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an octadecenoyl group.
+ MOP:0001134
+ has_participant: CHEBI:50499
+ deoctadecenoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an octadecenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an octadec-6-enoyl group.
+ MOP:0001135
+ has_participant: CHEBI:50497
+ deoctadec-6-enoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an octadec-6-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a petroselaidoyl group.
+ MOP:0001136
+ has_participant: CHEBI:32378
+ depetroselaidoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a petroselaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a petroselinoyl group.
+ MOP:0001137
+ has_participant: CHEBI:32376
+ depetroselinoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a petroselinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a vaccenoyl group.
+ MOP:0001138
+ has_participant: CHEBI:27261
+ devaccenoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cis-vaccenoyl group.
+ MOP:0001139
+ has_participant: CHEBI:23313
+ de-cis-vaccenoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cis-vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trans-vaccenoyl group.
+ MOP:0001140
+ has_participant: CHEBI:27080
+ de-trans-vaccenoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trans-vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an octadec-9-enoyl group.
+ MOP:0001141
+ has_participant: CHEBI:50500
+ deoctadec-9-enoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an octadec-9-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an oleoyl group.
+ MOP:0001142
+ has_participant: CHEBI:25667
+ deoleoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an oleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an elaidoyl group.
+ MOP:0001143
+ has_participant: CHEBI:23904
+ deelaidoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an elaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a margaroyl group.
+ MOP:0001144
+ has_participant: CHEBI:32367
+ demargaroylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a margaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a melissoyl group.
+ MOP:0001145
+ has_participant: CHEBI:31016
+ demelissoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a melissoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a myristoleoyl group.
+ MOP:0001146
+ has_participant: CHEBI:32371
+ demyristoleoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a myristoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an obtusiloyl group.
+ MOP:0001147
+ has_participant: CHEBI:33162
+ deobtusiloylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an obtusiloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a lignoceroyl group.
+ MOP:0001148
+ has_participant: CHEBI:31015
+ delignoceroylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a lignoceroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a linoleoyl group.
+ MOP:0001149
+ has_participant: CHEBI:32386
+ delinoleoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a linoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a parinaroyl group.
+ MOP:0001150
+ has_participant: CHEBI:50501
+ deparinaroylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cis-parinaroyl group.
+ MOP:0001151
+ has_participant: CHEBI:32415
+ de-cis-parinaroylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cis-parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trans-parinaroyl group.
+ MOP:0001152
+ has_participant: CHEBI:32417
+ de-trans-parinaroylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trans-parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a gamma-glutamyl group.
+ MOP:0001153
+ has_participant: CHEBI:24190
+ de-gamma-glutamylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-gamma-glutamyl group.
+ MOP:0001154
+ has_participant: CHEBI:32474
+ de-L-gamma-glutamylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-gamma-glutamyl group.
+ MOP:0001155
+ has_participant: CHEBI:32480
+ de-D-gamma-glutamylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glucuronosyl group.
+ MOP:0001156
+ has_participant: CHEBI:24303
+ deglucuronosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glucuronosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-glucuronoyl group.
+ MOP:0001157
+ has_participant: CHEBI:24307
+ de-D-glucuronoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-glucuronoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glyceroyl 2,3-dihydroxypropanoyl group.
+ MOP:0001158
+ has_participant: CHEBI:24363
+ deglyceroyl 2,3-dihydroxypropanoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glyceroyl 2,3-dihydroxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glyceryl group.
+ MOP:0001159
+ has_participant: CHEBI:24364
+ deglycerylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glyceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glycidoyl 2,3-epoxypropanoyl group.
+ MOP:0001160
+ has_participant: CHEBI:24365
+ deglycidoyl 2,3-epoxypropanoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glycidoyl 2,3-epoxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glycoloyl group.
+ MOP:0001161
+ has_participant: CHEBI:30884
+ deglycoloylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glycoloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glycosyl group.
+ MOP:0001162
+ has_participant: CHEBI:24403
+ deglycosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glycosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a galactosyl group.
+ MOP:0001163
+ has_participant: CHEBI:24164
+ degalactosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-D-galactosyl group.
+ MOP:0001168
+ MOP:0001164
+ has_participant: CHEBI:22778
+ de-beta-D-galactosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-L-fucosyl-1,2-beta-D-galactosyl group.
+ MOP:0001165
+ has_participant: CHEBI:16124
+ de-alpha-L-fucosyl-1,2-beta-D-galactosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-L-fucosyl-1,2-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ MOP:0001166
+ has_participant: CHEBI:16361
+ de-alpha-N-acetylneuraminyl-2,3-beta-D-galactosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ MOP:0001167
+ has_participant: CHEBI:17483
+ de-alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glucosyl group.
+ MOP:0001172
+ MOP:0001169
+ has_participant: CHEBI:24281
+ deglucosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosyl group.
+ MOP:0001170
+ has_participant: CHEBI:17227
+ de-D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-galactosyl-1,4beta-D-glucosyl group.
+ MOP:0001171
+ has_participant: CHEBI:20966
+ de-D-galactosyl-1,4beta-D-glucosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-galactosyl-1,4beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-glucosyl group.
+ MOP:0001173
+ has_participant: CHEBI:30684
+ de-alpha-glucosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-glucosyl group.
+ MOP:0001174
+ has_participant: CHEBI:30697
+ de-beta-glucosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-galactosyl-(1->4)-beta-D-glucosyl group.
+ MOP:0001175
+ has_participant: CHEBI:18018
+ de-D-galactosyl-(1->4)-beta-D-glucosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-galactosyl-(1->4)-beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glycosaminyl group.
+ MOP:0001176
+ has_participant: CHEBI:24399
+ deglycosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glycosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a galactosaminyl group.
+ MOP:0001177
+ has_participant: CHEBI:24160
+ degalactosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-D-galactosaminyl group.
+ MOP:0001178
+ has_participant: CHEBI:21507
+ de-N-acetyl-D-galactosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0001179
+ has_participant: CHEBI:17850
+ de-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ MOP:0001180
+ has_participant: CHEBI:16565
+ de-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ MOP:0001181
+ has_participant: CHEBI:16901
+ de-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0001182
+ has_participant: CHEBI:15876
+ de-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0001183
+ has_participant: CHEBI:17723
+ de-beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ MOP:0001184
+ has_participant: CHEBI:16117
+ de-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ MOP:0001185
+ has_participant: CHEBI:22783
+ de-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0001186
+ has_participant: CHEBI:17581
+ de-N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminyl group.
+ MOP:0001187
+ has_participant: CHEBI:16250
+ de-N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminyl group.
+ MOP:0001188
+ has_participant: CHEBI:16478
+ de-N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glucosaminyl group.
+ MOP:0001189
+ has_participant: CHEBI:24272
+ deglucosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-D-glucosaminyl group.
+ MOP:0001190
+ has_participant: CHEBI:21524
+ de-N-acetyl-D-glucosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ MOP:0001191
+ has_participant: CHEBI:18914
+ de-1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 3-O-beta-D-galactosyl-N-acetyl-D-glucosaminyl group.
+ MOP:0001192
+ has_participant: CHEBI:18915
+ de-3-O-beta-D-galactosyl-N-acetyl-D-glucosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 3-O-beta-D-galactosyl-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ MOP:0001193
+ has_participant: CHEBI:18939
+ de-1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0001194
+ has_participant: CHEBI:17571
+ de-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0001195
+ has_participant: CHEBI:17785
+ de-alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0001196
+ has_participant: CHEBI:22381
+ de-alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminyl group.
+ MOP:0001197
+ has_participant: CHEBI:22779
+ de-beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0001198
+ has_participant: CHEBI:21580
+ de-N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0001199
+ has_participant: CHEBI:21581
+ de-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0001200
+ has_participant: CHEBI:21582
+ de-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0001201
+ has_participant: CHEBI:21583
+ de-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0001202
+ has_participant: CHEBI:16059
+ de-N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0001203
+ has_participant: CHEBI:16198
+ de-N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an iduronosyl group.
+ MOP:0001204
+ has_participant: CHEBI:24770
+ deiduronosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an iduronosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-inosinyl group.
+ MOP:0001205
+ has_participant: CHEBI:24845
+ de-5'-inosinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-inosinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a mannosyl group.
+ MOP:0001209
+ MOP:0001206
+ has_participant: CHEBI:25171
+ demannosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a (N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ MOP:0001207
+ has_participant: CHEBI:18638
+ de-(N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a (N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-D-mannosyl-1,3-(r1)-beta-D-mannosyl group.
+ MOP:0001208
+ has_participant: CHEBI:22406
+ de-alpha-D-mannosyl-1,3-(r1)-beta-D-mannosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-D-mannosyl-1,3-(r1)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-mannosyl group.
+ MOP:0001210
+ has_participant: CHEBI:30689
+ de-alpha-mannosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosyl group.
+ MOP:0001211
+ has_participant: CHEBI:32618
+ de-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosyl group.
+ MOP:0001212
+ has_participant: CHEBI:32890
+ de-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ MOP:0001213
+ has_participant: CHEBI:21589
+ de-N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosyl group.
+ MOP:0001214
+ has_participant: CHEBI:32601
+ de-N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosyl group.
+ MOP:0001215
+ has_participant: CHEBI:32602
+ de-N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-D-mannosyl-(1->3)-beta-D-mannosyl group.
+ MOP:0001216
+ has_participant: CHEBI:32591
+ de-alpha-D-mannosyl-(1->3)-beta-D-mannosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-D-mannosyl-(1->3)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a neuraminosyl group.
+ MOP:0001217
+ has_participant: CHEBI:25509
+ deneuraminosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a neuraminosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a neuraminoyl group.
+ MOP:0001218
+ has_participant: CHEBI:25510
+ deneuraminoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a neuraminoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a ribosyl group.
+ MOP:0001221
+ MOP:0001219
+ has_participant: CHEBI:26566
+ deribosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a ribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an adenosinediphosphoribosyl group.
+ MOP:0001220
+ has_participant: CHEBI:22259
+ deadenosinediphosphoribosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an adenosinediphosphoribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-deoxyribosyl group.
+ MOP:0001222
+ has_participant: CHEBI:30720
+ de-2-deoxyribosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-deoxyribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sialosyl group.
+ MOP:0001223
+ has_participant: CHEBI:26668
+ desialosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sialosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a hemicystyl group.
+ MOP:0001224
+ has_participant: CHEBI:24492
+ dehemicystylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a hemicystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a mevalonoyl group.
+ MOP:0001225
+ has_participant: CHEBI:25353
+ demevalonoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a mevalonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a montanoyl group.
+ MOP:0001226
+ has_participant: CHEBI:25417
+ demontanoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a montanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a muramyl group.
+ MOP:0001227
+ has_participant: CHEBI:25433
+ demuramylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nucleotidyl group.
+ MOP:0001228
+ has_participant: CHEBI:25613
+ denucleotidylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nucleotidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-adenylyl group.
+ MOP:0001229
+ has_participant: CHEBI:22263
+ de-5'-adenylylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-adenylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-cytidylyl group.
+ MOP:0001230
+ has_participant: CHEBI:23526
+ de-5'-cytidylylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-cytidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-thymidylyl group.
+ MOP:0001231
+ has_participant: CHEBI:27003
+ de-5'-thymidylylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-thymidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-uridylyl group.
+ MOP:0001232
+ has_participant: CHEBI:27244
+ de-5'-uridylylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-uridylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-guanylyl group.
+ MOP:0001233
+ has_participant: CHEBI:24460
+ de-5'-guanylylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-guanylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-ribothymidylyl group.
+ MOP:0001234
+ has_participant: CHEBI:26569
+ de-5'-ribothymidylylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-ribothymidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-inosinylyl group.
+ MOP:0001235
+ has_participant: CHEBI:33512
+ de-5'-inosinylylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-inosinylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pantothenyl group.
+ MOP:0001236
+ has_participant: CHEBI:25850
+ depantothenylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pantothenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pantoyl group.
+ MOP:0001237
+ has_participant: CHEBI:25851
+ depantoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pantoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a peptidyl group.
+ MOP:0001238
+ has_participant: CHEBI:25907
+ depeptidylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a peptidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phthalyl group.
+ MOP:0001239
+ has_participant: CHEBI:26096
+ dephthalylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phthalyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a propionyl group.
+ MOP:0001240
+ has_participant: CHEBI:26294
+ depropionylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a propionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pyruvoyl group.
+ MOP:0001241
+ has_participant: CHEBI:45360
+ depyruvoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pyruvoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a retinoyl group.
+ MOP:0001242
+ has_participant: CHEBI:26539
+ deretinoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a retinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sialoyl group.
+ MOP:0001243
+ has_participant: CHEBI:26670
+ desialoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 3-carboxypropanoyl group.
+ MOP:0001244
+ has_participant: CHEBI:26810
+ de-3-carboxypropanoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 3-carboxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trienoyl group.
+ MOP:0001245
+ has_participant: CHEBI:27107
+ detrienoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an anilinocarbonyl group.
+ MOP:0001246
+ has_participant: CHEBI:30692
+ deanilinocarbonylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an anilinocarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pteroyl group.
+ MOP:0001247
+ has_participant: CHEBI:26379
+ depteroylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pteroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 3-carboxyprop-2-enoyl group.
+ MOP:0001248
+ has_participant: CHEBI:37953
+ de-3-carboxyprop-2-enoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a (Z)-3-carboxyprop-2-enoyl group.
+ MOP:0001249
+ has_participant: CHEBI:25122
+ de-(Z)-3-carboxyprop-2-enoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a (Z)-3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a (E)-3-carboxyprop-2-enoyl group.
+ MOP:0001250
+ has_participant: CHEBI:24126
+ de-(E)-3-carboxyprop-2-enoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a (E)-3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2,6-dichlorobenzoyl group.
+ MOP:0001251
+ has_participant: CHEBI:48625
+ de-2,6-dichlorobenzoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2,6-dichlorobenzoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-muramyl group.
+ MOP:0001252
+ has_participant: CHEBI:30701
+ de-alpha-muramylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-muramyl group.
+ MOP:0001253
+ has_participant: CHEBI:30702
+ de-beta-muramylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a beta-muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a dihydrolipoyl group.
+ MOP:0001254
+ has_participant: CHEBI:50488
+ dedihydrolipoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sinapoyl group.
+ MOP:0001255
+ has_participant: CHEBI:50561
+ desinapoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sinapoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carboxyacetyl group.
+ MOP:0001256
+ has_participant: CHEBI:50650
+ decarboxyacetylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carboxyacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a divalent carboacyl group.
+ MOP:0001257
+ has_participant: CHEBI:23855
+ dedivalent carboacylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a divalent carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an aspartoyl group.
+ MOP:0001258
+ has_participant: CHEBI:22663
+ deaspartoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-aspartoyl group.
+ MOP:0001259
+ has_participant: CHEBI:32464
+ de-L-aspartoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-aspartoyl group.
+ MOP:0001260
+ has_participant: CHEBI:32468
+ de-D-aspartoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a citraconoyl group.
+ MOP:0001261
+ has_participant: CHEBI:23315
+ decitraconoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a citraconoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glutamoyl group.
+ MOP:0001262
+ has_participant: CHEBI:24322
+ deglutamoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-glutamoyl group.
+ MOP:0001263
+ has_participant: CHEBI:32481
+ de-D-glutamoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-glutamoyl group.
+ MOP:0001264
+ has_participant: CHEBI:32475
+ de-L-glutamoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a maloyl group.
+ MOP:0001265
+ has_participant: CHEBI:25138
+ demaloylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a maloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phthaloyl group.
+ MOP:0001266
+ has_participant: CHEBI:26095
+ dephthaloylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phthaloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a succinyl group.
+ MOP:0001267
+ has_participant: CHEBI:37952
+ desuccinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a succinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a butenedioyl group.
+ MOP:0001268
+ has_participant: CHEBI:37954
+ debutenedioylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a butenedioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a fumaroyl group.
+ MOP:0001269
+ has_participant: CHEBI:24125
+ defumaroylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a fumaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a maleoyl group.
+ MOP:0001270
+ has_participant: CHEBI:25121
+ demaleoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a maleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a hexanedioyl group.
+ MOP:0001271
+ has_participant: CHEBI:48082
+ dehexanedioylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a hexanedioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a malonyl group.
+ MOP:0001272
+ has_participant: CHEBI:25134
+ demalonylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a malonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an ornithyl group.
+ MOP:0001273
+ has_participant: CHEBI:46929
+ deornithylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an ornithyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-ornithyl group.
+ MOP:0001274
+ has_participant: CHEBI:44700
+ de-L-ornithylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-ornithyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a half-cystyl group.
+ MOP:0001275
+ has_participant: CHEBI:30770
+ dehalf-cystylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a half-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-tyrosin-O(4)-yl group.
+ MOP:0001276
+ has_participant: CHEBI:32768
+ de-L-tyrosin-O(4)-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-threonin-O(3)-yl group.
+ MOP:0001277
+ has_participant: CHEBI:32825
+ de-L-threonin-O(3)-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an L-threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-tyrosin-O(4)-yl group.
+ MOP:0001278
+ has_participant: CHEBI:32780
+ de-D-tyrosin-O(4)-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-threonin-O(3)-yl group.
+ MOP:0001279
+ has_participant: CHEBI:32831
+ de-D-threonin-O(3)-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a D-threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tyrosin-O(4)-yl group.
+ MOP:0001280
+ has_participant: CHEBI:32788
+ detyrosin-O(4)-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a threonin-O(3)-yl group.
+ MOP:0001281
+ has_participant: CHEBI:26985
+ dethreonin-O(3)-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an oxalyl group.
+ MOP:0001282
+ has_participant: CHEBI:30870
+ deoxalylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an oxalyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a fumagillin-2-yl group.
+ MOP:0001283
+ has_participant: CHEBI:42601
+ defumagillin-2-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a fumagillin-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acetoacetyl group.
+ MOP:0001284
+ has_participant: CHEBI:48051
+ deacetoacetylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acetoacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-linolenoyl group.
+ MOP:0001285
+ has_participant: CHEBI:32388
+ de-alpha-linolenoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alpha-linolenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a gamma-linolenoyl group.
+ MOP:0001286
+ has_participant: CHEBI:32390
+ de-gamma-linolenoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a gamma-linolenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carbamimidoyl group.
+ MOP:0001287
+ has_participant: CHEBI:48090
+ decarbamimidoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carbamimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a formimidoyl group.
+ MOP:0001288
+ has_participant: CHEBI:24084
+ deformimidoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a formimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trifluoroacetyl group.
+ MOP:0001289
+ has_participant: CHEBI:45888
+ detrifluoroacetylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trifluoroacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carboxymethyl group.
+ MOP:0001290
+ has_participant: CHEBI:41402
+ decarboxymethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carboxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a methylenecarbonyl group.
+ MOP:0001291
+ has_participant: CHEBI:43923
+ demethylenecarbonylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a methylenecarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-hydroxyacetimidoyl group.
+ MOP:0001292
+ has_participant: CHEBI:48055
+ de-N-hydroxyacetimidoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-hydroxyacetimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acryloyl group.
+ MOP:0001293
+ has_participant: CHEBI:48077
+ deacryloylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acryloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tert-butoxycarbonyl group.
+ MOP:0001294
+ has_participant: CHEBI:48502
+ de-tert-butoxycarbonylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tert-butoxycarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfanediyl group.
+ MOP:0001295
+ has_participant: CHEBI:29830
+ desulfanediylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phenylsulfanyl group.
+ MOP:0001296
+ has_participant: CHEBI:48499
+ dephenylsulfanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phenylsulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a methylsulfanyl group.
+ MOP:0001297
+ has_participant: CHEBI:48563
+ demethylsulfanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a methylsulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfaniumyl group.
+ MOP:0001298
+ has_participant: CHEBI:36945
+ desulfaniumylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a disulfanidyl group.
+ MOP:0001299
+ has_participant: CHEBI:29838
+ dedisulfanidylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a disulfanidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a disulfanediyl group.
+ MOP:0001300
+ has_participant: CHEBI:29826
+ dedisulfanediylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a disulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a disulfanyl group.
+ MOP:0001301
+ has_participant: CHEBI:30605
+ dedisulfanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a disulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tetrasulfanyl group.
+ MOP:0001302
+ has_participant: CHEBI:30607
+ detetrasulfanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tetrasulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tetrasulfanediyl group.
+ MOP:0001303
+ has_participant: CHEBI:29836
+ detetrasulfanediylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tetrasulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trisulfanyl group.
+ MOP:0001304
+ has_participant: CHEBI:30606
+ detrisulfanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trisulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trisulfanediyl group.
+ MOP:0001305
+ has_participant: CHEBI:29834
+ detrisulfanediylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trisulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pentasulfanyl group.
+ MOP:0001306
+ has_participant: CHEBI:30608
+ depentasulfanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pentasulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a diselanyl group.
+ MOP:0001307
+ has_participant: CHEBI:30602
+ dediselanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a diselanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tellanyl group.
+ MOP:0001308
+ has_participant: CHEBI:30458
+ detellanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tellanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tellanediyl group.
+ MOP:0001309
+ has_participant: CHEBI:30455
+ detellanediylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tellanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tellaniumyl group.
+ MOP:0001310
+ has_participant: CHEBI:30447
+ detellaniumylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tellaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a ditellanyl group.
+ MOP:0001311
+ has_participant: CHEBI:30601
+ deditellanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a ditellanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an amidyl group.
+ MOP:0001312
+ has_participant: CHEBI:48373
+ deamidylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an amidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an azanediyl group.
+ MOP:0001313
+ has_participant: CHEBI:29343
+ deazanediylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an azanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-aminoethyl group.
+ MOP:0001314
+ has_participant: CHEBI:22502
+ de-2-aminoethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-aminoethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 4-aminobutyl group.
+ MOP:0001315
+ has_participant: CHEBI:50339
+ de-4-aminobutylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 4-aminobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an azanetriyl group.
+ MOP:0001316
+ has_participant: CHEBI:30228
+ deazanetriylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an azanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a hydrazine-1,2-diyl group.
+ MOP:0001317
+ has_participant: CHEBI:30098
+ dehydrazine-1,2-diylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a hydrazine-1,2-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a diazyn-1-ium-1-yl group.
+ MOP:0001318
+ has_participant: CHEBI:30108
+ dediazyn-1-ium-1-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a diazyn-1-ium-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phosphanetriyl group.
+ MOP:0001319
+ has_participant: CHEBI:30206
+ dephosphanetriylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phosphanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phosphanediyl group.
+ MOP:0001320
+ has_participant: CHEBI:29944
+ dephosphanediylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phosphanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phosphanyl group.
+ MOP:0001321
+ has_participant: CHEBI:29936
+ dephosphanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phosphanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a lambda(5)-phosphanyl group.
+ MOP:0001322
+ has_participant: CHEBI:30284
+ delambda(5)-phosphanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a lambda(5)-phosphanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phosphaniumyl group.
+ MOP:0001323
+ has_participant: CHEBI:30279
+ dephosphaniumylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phosphaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arsanyl group.
+ MOP:0001324
+ has_participant: CHEBI:29759
+ dearsanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arsanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arsanediyl group.
+ MOP:0001325
+ has_participant: CHEBI:29763
+ dearsanediylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arsanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arsanetriyl group.
+ MOP:0001326
+ has_participant: CHEBI:29766
+ dearsanetriylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arsanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arsaniumyl group.
+ MOP:0001327
+ has_participant: CHEBI:29842
+ dearsaniumylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arsaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a lambda(5)-arsanyl group.
+ MOP:0001328
+ has_participant: CHEBI:30273
+ delambda(5)-arsanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a lambda(5)-arsanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a stibaniumyl group.
+ MOP:0001329
+ has_participant: CHEBI:30291
+ destibaniumylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a stibaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a lambda(5)-stibanyl group.
+ MOP:0001330
+ has_participant: CHEBI:30293
+ delambda(5)-stibanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a lambda(5)-stibanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a boranyl group.
+ MOP:0001331
+ has_participant: CHEBI:33604
+ deboranylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a boranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a boranetriyl group.
+ MOP:0001332
+ has_participant: CHEBI:30169
+ deboranetriylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a boranetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a boranediyl group.
+ MOP:0001333
+ has_participant: CHEBI:38988
+ deboranediylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a boranediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a boranuidyl group.
+ MOP:0001334
+ has_participant: CHEBI:30159
+ deboranuidylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a boranuidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a germyl group.
+ MOP:0001335
+ has_participant: CHEBI:30542
+ degermylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a germyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a germanediyl group.
+ MOP:0001336
+ has_participant: CHEBI:30554
+ degermanediylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a germanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a germanetetrayl group.
+ MOP:0001337
+ has_participant: CHEBI:30547
+ degermanetetraylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a germanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a germanetriyl group.
+ MOP:0001338
+ has_participant: CHEBI:30544
+ degermanetriylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a germanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a silyl group.
+ MOP:0001339
+ has_participant: CHEBI:30541
+ desilylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a silyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a silanediyl group.
+ MOP:0001340
+ has_participant: CHEBI:30587
+ desilanediylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a silanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a silanetriyl group.
+ MOP:0001341
+ has_participant: CHEBI:30576
+ desilanetriylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a silanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a silanetetrayl group.
+ MOP:0001342
+ has_participant: CHEBI:30583
+ desilanetetraylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a silanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a disilanyl group.
+ MOP:0001343
+ has_participant: CHEBI:30594
+ dedisilanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a disilanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alumanyl group.
+ MOP:0001344
+ has_participant: CHEBI:30135
+ dealumanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alumanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a stannyl group.
+ MOP:0001345
+ has_participant: CHEBI:30540
+ destannylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a stannyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a stannanetriyl group.
+ MOP:0001346
+ has_participant: CHEBI:30575
+ destannanetriylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a stannanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a plumbanetriyl group.
+ MOP:0001347
+ has_participant: CHEBI:30577
+ deplumbanetriylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a plumbanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a plumbyl group.
+ MOP:0001348
+ has_participant: CHEBI:30543
+ deplumbylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a plumbyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a gallanyl group.
+ MOP:0001349
+ has_participant: CHEBI:37119
+ degallanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a gallanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an indiganyl group.
+ MOP:0001350
+ has_participant: CHEBI:30431
+ deindiganylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an indiganyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a thallanyl group.
+ MOP:0001351
+ has_participant: CHEBI:30442
+ dethallanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a thallanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phosphatidyl group.
+ MOP:0001352
+ has_participant: CHEBI:26025
+ dephosphatidylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phosphatidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nucleosidyl group.
+ MOP:0001353
+ has_participant: CHEBI:33494
+ denucleosidylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nucleosidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a guanosyl group.
+ MOP:0001354
+ has_participant: CHEBI:24459
+ deguanosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a guanosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an inosyl group.
+ MOP:0001355
+ has_participant: CHEBI:24849
+ deinosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an inosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a thymidyl group.
+ MOP:0001356
+ has_participant: CHEBI:27002
+ dethymidylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a thymidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an adenosyl group.
+ MOP:0001357
+ has_participant: CHEBI:33505
+ deadenosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an adenosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-adenosyl group.
+ MOP:0001358
+ has_participant: CHEBI:22261
+ de-5'-adenosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 5'-adenosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an uridyl group.
+ MOP:0001359
+ has_participant: CHEBI:27243
+ deuridylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an uridyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cytidyl group.
+ MOP:0001360
+ has_participant: CHEBI:23525
+ decytidylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cytidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a dolichyl group.
+ MOP:0001361
+ has_participant: CHEBI:23883
+ dedolichylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a dolichyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-trans,6-trans-farnesyl group.
+ MOP:0001362
+ has_participant: CHEBI:36535
+ de-2-trans,6-trans-farnesylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-trans,6-trans-farnesyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a margaryl group.
+ MOP:0001363
+ has_participant: CHEBI:32925
+ demargarylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a margaryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a methyl group.
+ MOP:0001364
+ has_participant: CHEBI:32875
+ demethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a methyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a methanetetrayl group.
+ MOP:0001365
+ has_participant: CHEBI:30039
+ demethanetetraylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a methanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a methanetriyl group.
+ MOP:0001366
+ has_participant: CHEBI:29433
+ demethanetriylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a methanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trichloromethyl group.
+ MOP:0001367
+ has_participant: CHEBI:30736
+ detrichloromethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trichloromethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trifluoromethyl group.
+ MOP:0001368
+ has_participant: CHEBI:50127
+ detrifluoromethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trifluoromethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alkyl group.
+ MOP:0001369
+ has_participant: CHEBI:22323
+ dealkylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a butyl group.
+ MOP:0001370
+ has_participant: CHEBI:41264
+ debutylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a ceryl group.
+ MOP:0001371
+ has_participant: CHEBI:23081
+ decerylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a ceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a decyl group.
+ MOP:0001372
+ has_participant: CHEBI:23580
+ dedecylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a decyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a dodecyl group.
+ MOP:0001373
+ has_participant: CHEBI:23870
+ dedodecylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a dodecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a heptyl group.
+ MOP:0001374
+ has_participant: CHEBI:24526
+ deheptylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a heptyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a hexyl group.
+ MOP:0001375
+ has_participant: CHEBI:24593
+ dehexylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a hexyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a myricyl group.
+ MOP:0001376
+ has_participant: CHEBI:25453
+ demyricylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a myricyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a myristyl group.
+ MOP:0001377
+ has_participant: CHEBI:25457
+ demyristylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a myristyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nonyl group.
+ MOP:0001378
+ has_participant: CHEBI:25589
+ denonylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an octyl group.
+ MOP:0001379
+ has_participant: CHEBI:25657
+ deoctylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an octyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a palmityl group.
+ MOP:0001380
+ has_participant: CHEBI:25842
+ depalmitylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a palmityl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pentyl group.
+ MOP:0001381
+ has_participant: CHEBI:25902
+ depentylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a propyl group.
+ MOP:0001382
+ has_participant: CHEBI:26308
+ depropylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a propyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a stearyl group.
+ MOP:0001383
+ has_participant: CHEBI:26755
+ destearylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a stearyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an isopropyl group.
+ MOP:0001384
+ has_participant: CHEBI:30353
+ deisopropylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an isopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an ethyl group.
+ de-ethylation
+ MOP:0001385
+ has_participant: CHEBI:37807
+ deethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an ethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an isobutyl group.
+ MOP:0001386
+ has_participant: CHEBI:30356
+ deisobutylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an isobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pentan-2-yl group.
+ MOP:0001387
+ has_participant: CHEBI:32880
+ depentan-2-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pentan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an isopentyl group.
+ MOP:0001388
+ has_participant: CHEBI:30359
+ deisopentylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an isopentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 3-methylbutan-2-yl group.
+ MOP:0001389
+ has_participant: CHEBI:32882
+ de-3-methylbutan-2-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 3-methylbutan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tert-pentyl group.
+ MOP:0001390
+ has_participant: CHEBI:30360
+ de-tert-pentylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tert-pentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a neopentyl group.
+ MOP:0001391
+ has_participant: CHEBI:30357
+ deneopentylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a neopentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an undecyl group.
+ MOP:0001392
+ has_participant: CHEBI:32900
+ deundecylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an undecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tridecyl group.
+ MOP:0001393
+ has_participant: CHEBI:32908
+ detridecylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tridecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pentadecyl group.
+ MOP:0001394
+ has_participant: CHEBI:32909
+ depentadecylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pentadecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nonadecyl group.
+ MOP:0001395
+ has_participant: CHEBI:32928
+ denonadecylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nonadecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arachidyl group.
+ MOP:0001396
+ has_participant: CHEBI:32930
+ dearachidylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arachidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a henicosyl group.
+ MOP:0001397
+ has_participant: CHEBI:32932
+ dehenicosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a henicosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a behenyl group.
+ MOP:0001398
+ has_participant: CHEBI:32933
+ debehenylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a behenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tricosyl group.
+ MOP:0001399
+ has_participant: CHEBI:32935
+ detricosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tricosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a lignoceryl group.
+ MOP:0001400
+ has_participant: CHEBI:32937
+ delignocerylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a lignoceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pentacosyl group.
+ MOP:0001401
+ has_participant: CHEBI:32939
+ depentacosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pentacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a heptacosyl group.
+ MOP:0001402
+ has_participant: CHEBI:32942
+ deheptacosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a heptacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a montanyl group.
+ MOP:0001403
+ has_participant: CHEBI:32944
+ demontanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a montanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nonacosyl group.
+ MOP:0001404
+ has_participant: CHEBI:32945
+ denonacosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nonacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sec-butyl group.
+ MOP:0001405
+ has_participant: CHEBI:45557
+ de-sec-butylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sec-butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tert-butyl group.
+ MOP:0001406
+ has_participant: CHEBI:30355
+ de-tert-butylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tert-butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pentan-3-yl group.
+ MOP:0001407
+ has_participant: CHEBI:32881
+ depentan-3-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a pentan-3-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-chloroethyl group.
+ MOP:0001408
+ has_participant: CHEBI:47553
+ de-2-chloroethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-chloroethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 1-chloroethyl group.
+ MOP:0001409
+ has_participant: CHEBI:48099
+ de-1-chloroethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 1-chloroethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a hydrocarbyl group.
+ MOP:0001410
+ has_participant: CHEBI:33248
+ dehydrocarbylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a hydrocarbyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an aryl group.
+ MOP:0001411
+ has_participant: CHEBI:33338
+ dearylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an aryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phenyl group.
+ MOP:0001412
+ has_participant: CHEBI:30396
+ dephenylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a biphenyl-4-yl group.
+ MOP:0001413
+ has_participant: CHEBI:35447
+ debiphenyl-4-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a biphenyl-4-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a naphthyl group.
+ MOP:0001414
+ has_participant: CHEBI:51140
+ denaphthylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 1-naphthyl group.
+ MOP:0001415
+ has_participant: CHEBI:51138
+ de-1-naphthylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 1-naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-naphthyl group.
+ MOP:0001416
+ has_participant: CHEBI:51139
+ de-2-naphthylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cycloalkyl group.
+ MOP:0001417
+ has_participant: CHEBI:33441
+ decycloalkylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cycloalkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cyclobutyl group.
+ MOP:0001418
+ has_participant: CHEBI:30376
+ decyclobutylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cyclobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cyclopropyl group.
+ MOP:0001419
+ has_participant: CHEBI:30364
+ decyclopropylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cyclopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alkenyl group.
+ MOP:0001420
+ has_participant: CHEBI:37614
+ dealkenylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alkenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an oleyl group.
+ MOP:0001421
+ has_participant: CHEBI:25670
+ deoleylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an oleyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an allyl group.
+ MOP:0001422
+ has_participant: CHEBI:30361
+ deallylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an allyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an isopropenyl group.
+ MOP:0001423
+ has_participant: CHEBI:30354
+ deisopropenylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an isopropenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a vinyl group.
+ MOP:0001424
+ has_participant: CHEBI:37603
+ devinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a vinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a prenyl group.
+ MOP:0001427
+ MOP:0001425
+ has_participant: CHEBI:26248
+ deprenylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a prenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phytyl group.
+ MOP:0001426
+ has_participant: CHEBI:26126
+ dephytylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phytyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a polyprenyl group.
+ MOP:0001428
+ has_participant: CHEBI:26201
+ depolyprenylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a polyprenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a farnesyl group.
+ MOP:0001429
+ has_participant: CHEBI:24017
+ defarnesylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a farnesyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a geranyl group.
+ MOP:0001430
+ has_participant: CHEBI:24224
+ degeranylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a geranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a geranylgeranyl group.
+ MOP:0001431
+ has_participant: CHEBI:24231
+ degeranylgeranylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a geranylgeranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a retinyl group.
+ MOP:0001432
+ has_participant: CHEBI:26541
+ deretinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a retinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an adamantan-2-yl group.
+ MOP:0001433
+ has_participant: CHEBI:48078
+ deadamantan-2-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an adamantan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cycloalkenyl group.
+ MOP:0001434
+ has_participant: CHEBI:48886
+ decycloalkenylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cycloalkenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a campholenic cyclohexenyl group.
+ MOP:0001435
+ has_participant: CHEBI:48885
+ decampholenic cyclohexenylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a campholenic cyclohexenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cyclopentadienyl group.
+ MOP:0001436
+ has_participant: CHEBI:30663
+ decyclopentadienylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an eta(5)-cyclopentadienyl group.
+ MOP:0001437
+ has_participant: CHEBI:36763
+ deeta(5)-cyclopentadienylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an eta(5)-cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an eta(1)-cyclopentadienyl group.
+ MOP:0001438
+ has_participant: CHEBI:36764
+ deeta(1)-cyclopentadienylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an eta(1)-cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an ethene-1,2-diyl group.
+ MOP:0001439
+ has_participant: CHEBI:46880
+ deethene-1,2-diylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an ethene-1,2-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arachidonyl group.
+ MOP:0001440
+ has_participant: CHEBI:22612
+ dearachidonylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arachidonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a benzyl group.
+ MOP:0001441
+ has_participant: CHEBI:22744
+ debenzylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a benzyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an anthracen-1-yl group.
+ MOP:0001442
+ has_participant: CHEBI:48287
+ deanthracen-1-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an anthracen-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an anthracen-2-yl group.
+ MOP:0001443
+ has_participant: CHEBI:48371
+ deanthracen-2-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an anthracen-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an imidazolyl group.
+ MOP:0001444
+ has_participant: CHEBI:50052
+ deimidazolylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an imidazolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an imidazol-1-yl group.
+ MOP:0001445
+ has_participant: CHEBI:50053
+ deimidazol-1-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an imidazol-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an imidazol-2-yl group.
+ MOP:0001446
+ has_participant: CHEBI:50054
+ deimidazol-2-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an imidazol-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an imidazol-5-yl group.
+ MOP:0001447
+ has_participant: CHEBI:50055
+ deimidazol-5-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an imidazol-5-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an imidazol-4-yl group.
+ MOP:0001448
+ has_participant: CHEBI:50056
+ deimidazol-4-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an imidazol-4-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a furyl group.
+ MOP:0001449
+ has_participant: CHEBI:24131
+ defurylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-furyl group.
+ MOP:0001450
+ has_participant: CHEBI:19586
+ de-2-furylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 3-furyl group.
+ MOP:0001451
+ has_participant: CHEBI:20025
+ de-3-furylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 3-furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a thienyl group.
+ MOP:0001452
+ has_participant: CHEBI:37991
+ dethienylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-thienyl group.
+ MOP:0001453
+ has_participant: CHEBI:35849
+ de-2-thienylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 3-thienyl group.
+ MOP:0001454
+ has_participant: CHEBI:37992
+ de-3-thienylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 3-thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an adenin-9-yl group.
+ MOP:0001455
+ has_participant: CHEBI:30756
+ deadenin-9-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an adenin-9-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a guanin-9-yl group.
+ MOP:0001456
+ has_participant: CHEBI:30755
+ deguanin-9-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a guanin-9-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acetimidoyl group.
+ MOP:0001457
+ has_participant: CHEBI:48050
+ deacetimidoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acetimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an organyl group.
+ MOP:0001458
+ has_participant: CHEBI:33249
+ deorganylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an organyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an organic heterocyclyl group.
+ MOP:0001459
+ has_participant: CHEBI:33453
+ deorganic heterocyclylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an organic heterocyclyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a heteroaryl group.
+ MOP:0001460
+ has_participant: CHEBI:33470
+ deheteroarylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a heteroaryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 4,4'-dimethoxytriphenylmethyl group.
+ MOP:0001461
+ has_participant: CHEBI:51095
+ de-4,4'-dimethoxytriphenylmethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 4,4'-dimethoxytriphenylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tauryl group.
+ MOP:0001462
+ has_participant: CHEBI:26861
+ detaurylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tauryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a triflyl group.
+ MOP:0001463
+ has_participant: CHEBI:48548
+ detriflylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a triflyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glycidyl group.
+ MOP:0001464
+ has_participant: CHEBI:24366
+ deglycidylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a glycidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfanylmethyl group.
+ MOP:0001465
+ has_participant: CHEBI:50326
+ desulfanylmethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfanylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a selanylmethyl group.
+ MOP:0001466
+ has_participant: CHEBI:50327
+ deselanylmethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a selanylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-carboxyethyl group.
+ MOP:0001467
+ has_participant: CHEBI:50329
+ de-2-carboxyethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-carboxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-amino-2-oxoethyl group.
+ MOP:0001468
+ has_participant: CHEBI:50330
+ de-2-amino-2-oxoethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-amino-2-oxoethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 3-amino-3-oxopropyl group.
+ MOP:0001469
+ has_participant: CHEBI:50331
+ de-3-amino-3-oxopropylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 3-amino-3-oxopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-(methylsulfanyl)ethyl group.
+ MOP:0001470
+ has_participant: CHEBI:50332
+ de-2-(methylsulfanyl)ethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-(methylsulfanyl)ethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 4-hydroxybenzyl group.
+ MOP:0001471
+ has_participant: CHEBI:50336
+ de-4-hydroxybenzylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 4-hydroxybenzyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 1H-indol-3-ylmethyl group.
+ MOP:0001472
+ has_participant: CHEBI:50337
+ de-1H-indol-3-ylmethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 1H-indol-3-ylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 1H-imidazol-4-ylmethyl group.
+ MOP:0001473
+ has_participant: CHEBI:50338
+ de-1H-imidazol-4-ylmethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 1H-imidazol-4-ylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 3-carbamimidamidopropyl group.
+ MOP:0001474
+ has_participant: CHEBI:50340
+ de-3-carbamimidamidopropylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 3-carbamimidamidopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a hydroxymethyl group.
+ MOP:0001475
+ has_participant: CHEBI:24712
+ dehydroxymethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a hydroxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 1-hydroxyethyl group.
+ MOP:0001476
+ has_participant: CHEBI:50341
+ de-1-hydroxyethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 1-hydroxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a haloalkyl group.
+ MOP:0001477
+ has_participant: CHEBI:50491
+ dehaloalkylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a haloalkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-(trimethylsilyl)ethoxymethyl group.
+ MOP:0001478
+ has_participant: CHEBI:51093
+ de-2-(trimethylsilyl)ethoxymethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-(trimethylsilyl)ethoxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acyl group.
+ MOP:0001479
+ has_participant: CHEBI:22221
+ deacylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an organoheteryl group.
+ MOP:0001480
+ has_participant: CHEBI:33456
+ deorganoheterylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an organoheteryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an oxalosulfanyl group.
+ MOP:0001481
+ has_participant: CHEBI:30874
+ deoxalosulfanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an oxalosulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an organosilyl group.
+ MOP:0001482
+ has_participant: CHEBI:33478
+ deorganosilylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an organosilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trimethylsilyl group.
+ MOP:0001483
+ has_participant: CHEBI:51088
+ detrimethylsilylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trimethylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a triisopropylsilyl group.
+ MOP:0001484
+ has_participant: CHEBI:51089
+ detriisopropylsilylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a triisopropylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tert-butyldiphenylsilyl group.
+ MOP:0001485
+ has_participant: CHEBI:51090
+ de-tert-butyldiphenylsilylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tert-butyldiphenylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tert-butyldimethylsilyl group.
+ MOP:0001486
+ has_participant: CHEBI:51091
+ de-tert-butyldimethylsilylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tert-butyldimethylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a thioacyl group.
+ MOP:0001487
+ has_participant: CHEBI:49063
+ dethioacylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a thioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carbothioacyl group.
+ MOP:0001488
+ has_participant: CHEBI:49066
+ decarbothioacylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an univalent carbothioacyl group.
+ MOP:0001489
+ has_participant: CHEBI:49067
+ deunivalent carbothioacylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an univalent carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a divalent carbothioacyl group.
+ MOP:0001490
+ has_participant: CHEBI:49068
+ dedivalent carbothioacylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a divalent carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carbonimidoyl group.
+ MOP:0001491
+ has_participant: CHEBI:29815
+ decarbonimidoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carbonimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a thiocarbonyl group.
+ MOP:0001492
+ has_participant: CHEBI:30256
+ dethiocarbonylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a thiocarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a (fluoren-9-ylmethoxy)carbonyl group.
+ MOP:0001493
+ has_participant: CHEBI:48605
+ de-(fluoren-9-ylmethoxy)carbonylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a (fluoren-9-ylmethoxy)carbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carbonyl group.
+ MOP:0001494
+ has_participant: CHEBI:23019
+ decarbonylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a carbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cytosin-1-yl group.
+ MOP:0001495
+ has_participant: CHEBI:30758
+ decytosin-1-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a cytosin-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a thymin-1-yl group.
+ MOP:0001496
+ has_participant: CHEBI:30757
+ dethymin-1-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a thymin-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an uracil-1-yl group.
+ MOP:0001497
+ has_participant: CHEBI:30759
+ deuracil-1-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an uracil-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a morpholin-4-ylsulfonyl group.
+ MOP:0001498
+ has_participant: CHEBI:45701
+ demorpholin-4-ylsulfonylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a morpholin-4-ylsulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acetohydrazonoyl group.
+ MOP:0001499
+ has_participant: CHEBI:48054
+ deacetohydrazonoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acetohydrazonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-hydroxyethyl group.
+ MOP:0001500
+ has_participant: CHEBI:44730
+ de-2-hydroxyethylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a 2-hydroxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an aminosulfinyl group.
+ MOP:0001501
+ has_participant: CHEBI:48257
+ deaminosulfinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an aminosulfinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a disiloxanyl group.
+ MOP:0001502
+ has_participant: CHEBI:48142
+ dedisiloxanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a disiloxanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a disiloxane-1,3-diyl group.
+ MOP:0001503
+ has_participant: CHEBI:48143
+ dedisiloxane-1,3-diylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a disiloxane-1,3-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an azinoyl group.
+ MOP:0001504
+ has_participant: CHEBI:29771
+ deazinoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an azinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an azonoyl group.
+ MOP:0001505
+ has_participant: CHEBI:37768
+ deazonoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an azonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phosphorothioyl group.
+ MOP:0001506
+ has_participant: CHEBI:32412
+ dephosphorothioylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phosphorothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phosphonothioyl group.
+ MOP:0001507
+ has_participant: CHEBI:32413
+ dephosphonothioylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phosphonothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arsonoyl group.
+ MOP:0001508
+ has_participant: CHEBI:29848
+ dearsonoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arsonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arsinoyl group.
+ MOP:0001509
+ has_participant: CHEBI:30277
+ dearsinoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arsinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a stiboryl group.
+ MOP:0001510
+ has_participant: CHEBI:48439
+ destiborylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a stiboryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfamoyl group.
+ MOP:0001511
+ has_participant: CHEBI:48266
+ desulfamoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a S-aminosulfinimidoyl group.
+ MOP:0001512
+ has_participant: CHEBI:48254
+ de-S-aminosulfinimidoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a S-aminosulfinimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a S-aminosulfonimidoyl group.
+ MOP:0001513
+ has_participant: CHEBI:48264
+ de-S-aminosulfonimidoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a S-aminosulfonimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a chloryl group.
+ MOP:0001514
+ has_participant: CHEBI:29883
+ dechlorylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a chloryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a chlorosyl group.
+ MOP:0001515
+ has_participant: CHEBI:29878
+ dechlorosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a chlorosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a perchloryl group.
+ MOP:0001516
+ has_participant: CHEBI:29877
+ deperchlorylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a perchloryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a bromosyl group.
+ MOP:0001517
+ has_participant: CHEBI:29871
+ debromosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a bromosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a bromyl group.
+ MOP:0001518
+ has_participant: CHEBI:29881
+ debromylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a bromyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a perbromyl group.
+ MOP:0001519
+ has_participant: CHEBI:29891
+ deperbromylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a perbromyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an iodosyl group.
+ MOP:0001520
+ has_participant: CHEBI:29897
+ deiodosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an iodosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an iodyl group.
+ MOP:0001521
+ has_participant: CHEBI:29904
+ deiodylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an iodyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a periodyl group.
+ MOP:0001522
+ has_participant: CHEBI:29908
+ deperiodylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a periodyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a fluorosyl group.
+ MOP:0001523
+ has_participant: CHEBI:30241
+ defluorosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a fluorosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfonyl group.
+ MOP:0001539
+ MOP:0001524
+ has_participant: CHEBI:29825
+ desulfonylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acetoxysulfonyl group.
+ MOP:0001525
+ has_participant: CHEBI:48065
+ deacetoxysulfonylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an acetoxysulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfonothioyl group.
+ MOP:0001526
+ has_participant: CHEBI:29828
+ desulfonothioylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfonothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfinothioyl group.
+ MOP:0001527
+ has_participant: CHEBI:29827
+ desulfinothioylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfinothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfonodithioyl group.
+ MOP:0001528
+ has_participant: CHEBI:29835
+ desulfonodithioylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfonodithioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trioxidanyl group.
+ MOP:0001529
+ has_participant: CHEBI:29791
+ detrioxidanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trioxidanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trioxidanediyl group.
+ MOP:0001530
+ has_participant: CHEBI:30493
+ detrioxidanediylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a trioxidanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a heterocyclyl group.
+ MOP:0001531
+ has_participant: CHEBI:48271
+ deheterocyclylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a heterocyclyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phosphoramidochloridoyl group.
+ MOP:0001532
+ has_participant: CHEBI:48229
+ dephosphoramidochloridoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a phosphoramidochloridoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a S-aminosulfonodiimidoyl group.
+ MOP:0001533
+ has_participant: CHEBI:48265
+ de-S-aminosulfonodiimidoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a S-aminosulfonodiimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an aminosulfanyl group.
+ MOP:0001534
+ has_participant: CHEBI:48252
+ deaminosulfanylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an aminosulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfinyl group.
+ MOP:0001535
+ has_participant: CHEBI:29822
+ desulfinylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arsoryl group.
+ MOP:0001536
+ has_participant: CHEBI:30274
+ dearsorylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an arsoryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an azanediidyl group.
+ MOP:0001537
+ has_participant: CHEBI:30227
+ deazanediidylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an azanediidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfinimidoyl group.
+ MOP:0001538
+ has_participant: CHEBI:29829
+ desulfinimidoylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfinimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tosyl group.
+ MOP:0001540
+ has_participant: CHEBI:51094
+ detosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a tosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a brosyl group.
+ MOP:0001541
+ has_participant: CHEBI:51101
+ debrosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a brosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nosyl group.
+ MOP:0001542
+ has_participant: CHEBI:51102
+ denosylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an indolyl group.
+ MOP:0001544
+ has_participant: CHEBI:51609
+ deindolylamination
+
+
+
+
+ Breaking of a covalent bond between a substrate and an indolyl group.
+ RSC:xp
+ rsc:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an indol-1-yl group.
+ MOP:0001545
+ has_participant: CHEBI:51610
+ deindol-1-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an indol-1-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an indol-2-yl group.
+ MOP:0001546
+ has_participant: CHEBI:51611
+ deindol-2-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an indol-2-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an indol-3-yl group.
+ MOP:0001547
+ has_participant: CHEBI:51612
+ deindol-3-ylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an indol-3-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-oxindolyl group.
+ MOP:0001548
+ has_participant: CHEBI:51613
+ de-N-oxindolylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an N-oxindolyl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alkylamino group.
+ MOP:0001549
+ has_participant: CHEBI:22332
+ dealkylamination
+
+
+
+
+ Breaking of a covalent bond between a substrate and an alkylamino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a halo group.
+ MOP:0001550
+ has_participant: CHEBI:47854
+ dehalogenation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a halo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a bromo group.
+ MOP:0001551
+ has_participant: CHEBI:47265
+ debromination
+
+
+
+
+ Breaking of a covalent bond between a substrate and a bromo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a chloro group.
+ MOP:0001552
+ has_participant: CHEBI:47853
+ dechlorination
+
+
+
+
+ Breaking of a covalent bond between a substrate and a chloro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a fluoro group.
+ MOP:0001553
+ has_participant: CHEBI:42645
+ defluorination
+
+
+
+
+ Breaking of a covalent bond between a substrate and a fluoro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an iodo group.
+ MOP:0001554
+ has_participant: CHEBI:43448
+ deiodination
+
+
+
+
+ Breaking of a covalent bond between a substrate and an iodo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an imino group.
+ MOP:0001555
+ has_participant: CHEBI:29342
+ deimination
+
+
+
+
+ Breaking of a covalent bond between a substrate and an imino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nitro group.
+ MOP:0001556
+ has_participant: CHEBI:29785
+ denitration
+
+
+
+
+ Breaking of a covalent bond between a substrate and a nitro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a hydroxyamino group.
+ MOP:0001557
+ has_participant: CHEBI:29769
+ dehydroxyamination
+
+
+
+
+ Breaking of a covalent bond between a substrate and a hydroxyamino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a thioxo group.
+ MOP:0001558
+ has_participant: CHEBI:29833
+ dethioxonation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a thioxo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfo group.
+ MOP:0001559
+ has_participant: CHEBI:29922
+ desulfonation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a sulfo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a selenono group.
+ MOP:0001560
+ has_participant: CHEBI:29923
+ deselenonation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a selenono group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a boryl group (-BR'R').
+ MOP:0002000
+ Submitted to ChEBI
+ N-borylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a boryl group (-BR'R').
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a methanidyl group.
+ MOP:0002001
+ has_participant: CHEBI:29361
+ N-methanidylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a methanidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an azaniumyl group.
+ MOP:0002002
+ has_participant: CHEBI:48284
+ N-azaniumylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an azaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a formyl group.
+ MOP:0002003
+ has_participant: CHEBI:42485
+ N-formylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a formyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acetonyl group.
+ MOP:0002004
+ has_participant: CHEBI:48056
+ N-acetonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acetonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-cystyl group.
+ MOP:0002005
+ has_participant: CHEBI:50057
+ N-L-cystylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-cystinyl group.
+ MOP:0002006
+ has_participant: CHEBI:50066
+ N-L-cystinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-cystinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-cystyl group.
+ MOP:0002007
+ has_participant: CHEBI:50049
+ N-D-cystylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cystinyl group.
+ MOP:0002008
+ has_participant: CHEBI:50050
+ N-cystinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cystinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cystyl group.
+ MOP:0002009
+ has_participant: CHEBI:23514
+ N-cystylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cysteinyl group.
+ MOP:0002010
+ has_participant: CHEBI:23511
+ N-cysteinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-cysteinyl group.
+ MOP:0002011
+ has_participant: CHEBI:32447
+ N-L-cysteinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-cysteinyl group.
+ MOP:0002012
+ has_participant: CHEBI:32452
+ N-D-cysteinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cystein-S-yl group.
+ MOP:0002013
+ has_participant: CHEBI:32795
+ N-cystein-S-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-cystein-S-yl group.
+ MOP:0002014
+ has_participant: CHEBI:32794
+ N-D-cystein-S-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-cystein-S-yl group.
+ MOP:0002015
+ has_participant: CHEBI:32793
+ N-L-cystein-S-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a methionyl group.
+ MOP:0002016
+ has_participant: CHEBI:37902
+ N-methionylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-methionyl group.
+ MOP:0002017
+ has_participant: CHEBI:49038
+ N-L-methionylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-formyl-L-methionyl group.
+ MOP:0002018
+ has_participant: CHEBI:49298
+ N-N-formyl-L-methionylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-formyl-L-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-methionyl group.
+ MOP:0002019
+ has_participant: CHEBI:32640
+ N-D-methionylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an (R)-lipoyl group.
+ MOP:0002020
+ has_participant: CHEBI:38232
+ N-(R)-lipoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an (R)-lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an (S)-lipoyl group.
+ MOP:0002021
+ has_participant: CHEBI:38233
+ N-(S)-lipoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an (S)-lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a lipoyl group.
+ MOP:0002022
+ has_participant: CHEBI:25064
+ N-lipoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an (R)-dihydrolipoyl group.
+ MOP:0002023
+ has_participant: CHEBI:30319
+ N-(R)-dihydrolipoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an (R)-dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an (S)-dihydrolipoyl group.
+ MOP:0002024
+ has_participant: CHEBI:50489
+ N-(S)-dihydrolipoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an (S)-dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-sialoyl group.
+ MOP:0002025
+ has_participant: CHEBI:32960
+ N-alpha-sialoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-sialoyl group.
+ MOP:0002026
+ has_participant: CHEBI:32961
+ N-beta-sialoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glyceroyl group.
+ MOP:0002027
+ has_participant: CHEBI:30750
+ N-glyceroylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glyceroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carboacyl group.
+ MOP:0002028
+ has_participant: CHEBI:37838
+ N-carboacylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an univalent carboacyl group.
+ MOP:0002029
+ has_participant: CHEBI:27207
+ N-univalent carboacylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an univalent carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acetyl group.
+ MOP:0002030
+ has_participant: CHEBI:40574
+ N-acetylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-aminoacyl group.
+ MOP:0002031
+ has_participant: CHEBI:22487
+ N-alpha-aminoacylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-aminoacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alanyl group.
+ MOP:0002032
+ has_participant: CHEBI:22280
+ N-alanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-alanyl group.
+ MOP:0002033
+ has_participant: CHEBI:32433
+ N-L-alanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-alanyl group.
+ MOP:0002034
+ has_participant: CHEBI:32437
+ N-D-alanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-aspartyl group.
+ MOP:0002035
+ has_participant: CHEBI:22445
+ N-alpha-aspartylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-alpha-aspartyl group.
+ MOP:0002036
+ has_participant: CHEBI:32462
+ N-L-alpha-aspartylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-alpha-aspartyl group.
+ MOP:0002037
+ has_participant: CHEBI:32466
+ N-D-alpha-aspartylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-glutamyl group.
+ MOP:0002038
+ has_participant: CHEBI:22453
+ N-alpha-glutamylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-alpha-glutamyl group.
+ MOP:0002039
+ has_participant: CHEBI:46855
+ N-L-alpha-glutamylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-alpha-glutamyl group.
+ MOP:0002040
+ has_participant: CHEBI:32479
+ N-D-alpha-glutamylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pteroylglutamyl group.
+ MOP:0002041
+ has_participant: CHEBI:26380
+ N-pteroylglutamylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pteroylglutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phenylalanyl group.
+ MOP:0002042
+ has_participant: CHEBI:25987
+ N-phenylalanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-phenylalanyl group.
+ MOP:0002043
+ has_participant: CHEBI:32496
+ N-L-phenylalanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-phenylalanyl group.
+ MOP:0002044
+ has_participant: CHEBI:32500
+ N-D-phenylalanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glycyl group.
+ MOP:0002045
+ has_participant: CHEBI:46740
+ N-glycylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glycyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a histidyl group.
+ MOP:0002046
+ has_participant: CHEBI:37906
+ N-histidylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-histidyl group.
+ MOP:0002047
+ has_participant: CHEBI:32514
+ N-L-histidylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-histidyl group.
+ MOP:0002048
+ has_participant: CHEBI:32522
+ N-D-histidylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an isoleucyl group.
+ MOP:0002049
+ has_participant: CHEBI:37905
+ N-isoleucylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-isoleucyl group.
+ MOP:0002050
+ has_participant: CHEBI:32606
+ N-L-isoleucylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-isoleucyl group.
+ MOP:0002051
+ has_participant: CHEBI:32610
+ N-D-isoleucylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a lysyl group.
+ MOP:0002052
+ has_participant: CHEBI:37903
+ N-lysylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-lysyl group.
+ MOP:0002053
+ has_participant: CHEBI:32553
+ N-L-lysylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a deoxyhypusinyl group.
+ MOP:0002054
+ has_participant: CHEBI:50039
+ N-deoxyhypusinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a deoxyhypusinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-lysyl group.
+ MOP:0002055
+ has_participant: CHEBI:32559
+ N-D-lysylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a leucyl group.
+ MOP:0002056
+ has_participant: CHEBI:37904
+ N-leucylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-leucyl group.
+ MOP:0002057
+ has_participant: CHEBI:32621
+ N-L-leucylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-leucyl group.
+ MOP:0002058
+ has_participant: CHEBI:32625
+ N-D-leucylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an asparaginyl group.
+ MOP:0002059
+ has_participant: CHEBI:22656
+ N-asparaginylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-asparaginyl group.
+ MOP:0002060
+ has_participant: CHEBI:50348
+ N-L-asparaginylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-asparaginyl group.
+ MOP:0002061
+ has_participant: CHEBI:32653
+ N-D-asparaginylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a prolyl group.
+ MOP:0002062
+ has_participant: CHEBI:26274
+ N-prolylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-prolyl group.
+ MOP:0002063
+ has_participant: CHEBI:32865
+ N-L-prolylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-prolyl group.
+ MOP:0002064
+ has_participant: CHEBI:32869
+ N-D-prolylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glutaminyl group.
+ MOP:0002065
+ has_participant: CHEBI:24320
+ N-glutaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-glutaminyl group.
+ MOP:0002066
+ has_participant: CHEBI:32667
+ N-L-glutaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-glutaminyl group.
+ MOP:0002067
+ has_participant: CHEBI:32674
+ N-D-glutaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a seryl group.
+ MOP:0002068
+ has_participant: CHEBI:37901
+ N-serylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-seryl group.
+ MOP:0002069
+ has_participant: CHEBI:32838
+ N-L-serylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-seryl group.
+ MOP:0002070
+ has_participant: CHEBI:32842
+ N-D-serylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a threonyl group.
+ MOP:0002071
+ has_participant: CHEBI:37900
+ N-threonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-threonyl group.
+ MOP:0002072
+ has_participant: CHEBI:32823
+ N-L-threonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-threonyl group.
+ MOP:0002073
+ has_participant: CHEBI:32829
+ N-D-threonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a selenocysteinyl group.
+ MOP:0002074
+ has_participant: CHEBI:32755
+ N-selenocysteinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-selenocysteinyl group.
+ MOP:0002075
+ has_participant: CHEBI:32745
+ N-L-selenocysteinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-selenocysteinyl group.
+ MOP:0002076
+ has_participant: CHEBI:32749
+ N-D-selenocysteinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a valyl group.
+ MOP:0002077
+ has_participant: CHEBI:37897
+ N-valylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-valyl group.
+ MOP:0002078
+ has_participant: CHEBI:32853
+ N-L-valylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-valyl group.
+ MOP:0002079
+ has_participant: CHEBI:32857
+ N-D-valylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tryptophyl group.
+ MOP:0002080
+ has_participant: CHEBI:37899
+ N-tryptophylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-tryptophyl group.
+ MOP:0002081
+ has_participant: CHEBI:32706
+ N-L-tryptophylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-tryptophyl group.
+ MOP:0002082
+ has_participant: CHEBI:32718
+ N-D-tryptophylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tyrosyl group.
+ MOP:0002083
+ has_participant: CHEBI:37898
+ N-tyrosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-tyrosyl group.
+ MOP:0002084
+ has_participant: CHEBI:32764
+ N-L-tyrosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-tyrosyl group.
+ MOP:0002085
+ has_participant: CHEBI:32778
+ N-D-tyrosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arginyl group.
+ MOP:0002086
+ has_participant: CHEBI:22619
+ N-arginylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-arginyl group.
+ MOP:0002087
+ has_participant: CHEBI:32684
+ N-L-arginylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-arginyl group.
+ MOP:0002088
+ has_participant: CHEBI:32691
+ N-D-arginylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a benzoyl group.
+ MOP:0002089
+ has_participant: CHEBI:22733
+ N-benzoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a benzoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-aspartyl group.
+ MOP:0002090
+ has_participant: CHEBI:22832
+ N-beta-aspartylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-beta-aspartyl group.
+ MOP:0002091
+ has_participant: CHEBI:32467
+ N-D-beta-aspartylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-beta-aspartyl group.
+ MOP:0002092
+ has_participant: CHEBI:48098
+ N-L-beta-aspartylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a biotinyl group.
+ MOP:0002093
+ has_participant: CHEBI:22885
+ N-biotinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a biotinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a butyryl group.
+ MOP:0002094
+ has_participant: CHEBI:22972
+ N-butyrylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a butyryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carbamoyl group.
+ MOP:0002095
+ has_participant: CHEBI:23004
+ N-carbamoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carbamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a C-aminocarbonohydrazonoyl group.
+ MOP:0002096
+ has_participant: CHEBI:48223
+ N-C-aminocarbonohydrazonoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a C-aminocarbonohydrazonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-(aminomethylidene)hydrazinyl group.
+ MOP:0002097
+ has_participant: CHEBI:48244
+ N-2-(aminomethylidene)hydrazinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-(aminomethylidene)hydrazinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carbamoylcarbamoyl group.
+ MOP:0002098
+ has_participant: CHEBI:48083
+ N-carbamoylcarbamoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carbamoylcarbamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carbamothioyl group.
+ MOP:0002099
+ has_participant: CHEBI:48225
+ N-carbamothioylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carbamothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acetylazanediyl group.
+ MOP:0002100
+ has_participant: CHEBI:48073
+ N-acetylazanediylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acetylazanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an oxamoyl group.
+ MOP:0002101
+ has_participant: CHEBI:48246
+ N-oxamoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an oxamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cholyl group.
+ MOP:0002102
+ has_participant: CHEBI:23220
+ N-cholylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cholyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an enoyl group.
+ MOP:0002103
+ has_participant: CHEBI:23916
+ N-enoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a fatty-acyl group.
+ MOP:0002104
+ has_participant: CHEBI:24027
+ N-fatty-acylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a fatty-acyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arachidonoyl group.
+ MOP:0002105
+ has_participant: CHEBI:22610
+ N-arachidonoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arachidonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arachidoyl group.
+ MOP:0002106
+ has_participant: CHEBI:22614
+ N-arachidoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arachidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a behenoyl group.
+ MOP:0002107
+ has_participant: CHEBI:22696
+ N-behenoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a behenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cerotoyl group.
+ MOP:0002108
+ has_participant: CHEBI:23080
+ N-cerotoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cerotoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a decanoyl group.
+ MOP:0002109
+ has_participant: CHEBI:23574
+ N-decanoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a decanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a dodecenoyl group.
+ MOP:0002110
+ has_participant: CHEBI:23868
+ N-dodecenoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a dodecenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an eleostearoyl group.
+ MOP:0002111
+ has_participant: CHEBI:23908
+ N-eleostearoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an eleostearoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a mycolyl group.
+ MOP:0002112
+ has_participant: CHEBI:25439
+ N-mycolylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a mycolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nervonoyl group.
+ MOP:0002113
+ has_participant: CHEBI:25503
+ N-nervonoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nervonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an octanoyl group.
+ MOP:0002114
+ has_participant: CHEBI:25650
+ N-octanoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an octanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a palmitoleoyl group.
+ MOP:0002115
+ has_participant: CHEBI:25837
+ N-palmitoleoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a palmitoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a palmitoyl group.
+ MOP:0002116
+ has_participant: CHEBI:45021
+ N-palmitoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a palmitoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a stearoyl group.
+ MOP:0002117
+ has_participant: CHEBI:26753
+ N-stearoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a stearoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an undecanoyl group.
+ MOP:0002118
+ has_participant: CHEBI:27190
+ N-undecanoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an undecanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a valeryl group.
+ MOP:0002119
+ has_participant: CHEBI:27265
+ N-valerylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a valeryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a hexanoyl group.
+ MOP:0002120
+ has_participant: CHEBI:24574
+ N-hexanoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a hexanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a heptanoyl group.
+ MOP:0002121
+ has_participant: CHEBI:32363
+ N-heptanoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a heptanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nonanoyl group.
+ MOP:0002122
+ has_participant: CHEBI:25580
+ N-nonanoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nonanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a lauroyl group.
+ MOP:0002123
+ has_participant: CHEBI:32359
+ N-lauroylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a lauroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a myristoyl group.
+ MOP:0002124
+ has_participant: CHEBI:25456
+ N-myristoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a myristoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a docosenoyl group.
+ MOP:0002125
+ has_participant: CHEBI:50479
+ N-docosenoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a docosenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cetoleoyl group.
+ MOP:0002126
+ has_participant: CHEBI:32430
+ N-cetoleoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cetoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an erucoyl group.
+ MOP:0002127
+ has_participant: CHEBI:32394
+ N-erucoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an erucoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an icosenoyl group.
+ MOP:0002128
+ has_participant: CHEBI:50480
+ N-icosenoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an icosenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a gadelaidoyl group.
+ MOP:0002129
+ has_participant: CHEBI:32424
+ N-gadelaidoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a gadelaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a gadoleoyl group.
+ MOP:0002130
+ has_participant: CHEBI:32421
+ N-gadoleoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a gadoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a gondoyl group.
+ MOP:0002131
+ has_participant: CHEBI:32427
+ N-gondoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a gondoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a heptatrienoyl group.
+ MOP:0002132
+ has_participant: CHEBI:50486
+ N-heptatrienoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a heptatrienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trans,trans-hepta-2,4,6-trienoyl group.
+ MOP:0002133
+ has_participant: CHEBI:30771
+ N-trans,trans-hepta-2,4,6-trienoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trans,trans-hepta-2,4,6-trienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an octadecenoyl group.
+ MOP:0002134
+ has_participant: CHEBI:50499
+ N-octadecenoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an octadecenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an octadec-6-enoyl group.
+ MOP:0002135
+ has_participant: CHEBI:50497
+ N-octadec-6-enoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an octadec-6-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a petroselaidoyl group.
+ MOP:0002136
+ has_participant: CHEBI:32378
+ N-petroselaidoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a petroselaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a petroselinoyl group.
+ MOP:0002137
+ has_participant: CHEBI:32376
+ N-petroselinoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a petroselinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a vaccenoyl group.
+ MOP:0002138
+ has_participant: CHEBI:27261
+ N-vaccenoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cis-vaccenoyl group.
+ MOP:0002139
+ has_participant: CHEBI:23313
+ N-cis-vaccenoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cis-vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trans-vaccenoyl group.
+ MOP:0002140
+ has_participant: CHEBI:27080
+ N-trans-vaccenoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trans-vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an octadec-9-enoyl group.
+ MOP:0002141
+ has_participant: CHEBI:50500
+ N-octadec-9-enoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an octadec-9-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an oleoyl group.
+ MOP:0002142
+ has_participant: CHEBI:25667
+ N-oleoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an oleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an elaidoyl group.
+ MOP:0002143
+ has_participant: CHEBI:23904
+ N-elaidoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an elaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a margaroyl group.
+ MOP:0002144
+ has_participant: CHEBI:32367
+ N-margaroylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a margaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a melissoyl group.
+ MOP:0002145
+ has_participant: CHEBI:31016
+ N-melissoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a melissoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a myristoleoyl group.
+ MOP:0002146
+ has_participant: CHEBI:32371
+ N-myristoleoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a myristoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an obtusiloyl group.
+ MOP:0002147
+ has_participant: CHEBI:33162
+ N-obtusiloylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an obtusiloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a lignoceroyl group.
+ MOP:0002148
+ has_participant: CHEBI:31015
+ N-lignoceroylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a lignoceroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a linoleoyl group.
+ MOP:0002149
+ has_participant: CHEBI:32386
+ N-linoleoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a linoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a parinaroyl group.
+ MOP:0002150
+ has_participant: CHEBI:50501
+ N-parinaroylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cis-parinaroyl group.
+ MOP:0002151
+ has_participant: CHEBI:32415
+ N-cis-parinaroylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cis-parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trans-parinaroyl group.
+ MOP:0002152
+ has_participant: CHEBI:32417
+ N-trans-parinaroylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trans-parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a gamma-glutamyl group.
+ MOP:0002153
+ has_participant: CHEBI:24190
+ N-gamma-glutamylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-gamma-glutamyl group.
+ MOP:0002154
+ has_participant: CHEBI:32474
+ N-L-gamma-glutamylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-gamma-glutamyl group.
+ MOP:0002155
+ has_participant: CHEBI:32480
+ N-D-gamma-glutamylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glucuronosyl group.
+ MOP:0002156
+ has_participant: CHEBI:24303
+ N-glucuronosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glucuronosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-glucuronoyl group.
+ MOP:0002157
+ has_participant: CHEBI:24307
+ N-D-glucuronoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-glucuronoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glyceroyl 2,3-dihydroxypropanoyl group.
+ MOP:0002158
+ has_participant: CHEBI:24363
+ N-glyceroyl 2,3-dihydroxypropanoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glyceroyl 2,3-dihydroxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glyceryl group.
+ MOP:0002159
+ has_participant: CHEBI:24364
+ N-glycerylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glyceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glycidoyl 2,3-epoxypropanoyl group.
+ MOP:0002160
+ has_participant: CHEBI:24365
+ N-glycidoyl 2,3-epoxypropanoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glycidoyl 2,3-epoxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glycoloyl group.
+ MOP:0002161
+ has_participant: CHEBI:30884
+ N-glycoloylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glycoloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glycosyl group.
+ MOP:0002162
+ has_participant: CHEBI:24403
+ N-glycosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glycosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a galactosyl group.
+ MOP:0002163
+ has_participant: CHEBI:24164
+ N-galactosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-D-galactosyl group.
+ MOP:0002168
+ MOP:0002164
+ has_participant: CHEBI:22778
+ N-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-L-fucosyl-1,2-beta-D-galactosyl group.
+ MOP:0002165
+ has_participant: CHEBI:16124
+ N-alpha-L-fucosyl-1,2-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-L-fucosyl-1,2-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ MOP:0002166
+ has_participant: CHEBI:16361
+ N-alpha-N-acetylneuraminyl-2,3-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ MOP:0002167
+ has_participant: CHEBI:17483
+ N-alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glucosyl group.
+ MOP:0002172
+ MOP:0002169
+ has_participant: CHEBI:24281
+ N-glucosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosyl group.
+ MOP:0002170
+ has_participant: CHEBI:17227
+ N-D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-galactosyl-1,4beta-D-glucosyl group.
+ MOP:0002171
+ has_participant: CHEBI:20966
+ N-D-galactosyl-1,4beta-D-glucosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-galactosyl-1,4beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-glucosyl group.
+ MOP:0002173
+ has_participant: CHEBI:30684
+ N-alpha-glucosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-glucosyl group.
+ MOP:0002174
+ has_participant: CHEBI:30697
+ N-beta-glucosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-galactosyl-(1->4)-beta-D-glucosyl group.
+ MOP:0002175
+ has_participant: CHEBI:18018
+ N-D-galactosyl-(1->4)-beta-D-glucosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-galactosyl-(1->4)-beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glycosaminyl group.
+ MOP:0002176
+ has_participant: CHEBI:24399
+ N-glycosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glycosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a galactosaminyl group.
+ MOP:0002177
+ has_participant: CHEBI:24160
+ N-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-D-galactosaminyl group.
+ MOP:0002178
+ has_participant: CHEBI:21507
+ N-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0002179
+ has_participant: CHEBI:17850
+ N-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ MOP:0002180
+ has_participant: CHEBI:16565
+ N-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ MOP:0002181
+ has_participant: CHEBI:16901
+ N-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0002182
+ has_participant: CHEBI:15876
+ N-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0002183
+ has_participant: CHEBI:17723
+ N-beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ MOP:0002184
+ has_participant: CHEBI:16117
+ N-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ MOP:0002185
+ has_participant: CHEBI:22783
+ N-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0002186
+ has_participant: CHEBI:17581
+ N-N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminyl group.
+ MOP:0002187
+ has_participant: CHEBI:16250
+ N-N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminyl group.
+ MOP:0002188
+ has_participant: CHEBI:16478
+ N-N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glucosaminyl group.
+ MOP:0002189
+ has_participant: CHEBI:24272
+ N-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-D-glucosaminyl group.
+ MOP:0002190
+ has_participant: CHEBI:21524
+ N-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ MOP:0002191
+ has_participant: CHEBI:18914
+ N-1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 3-O-beta-D-galactosyl-N-acetyl-D-glucosaminyl group.
+ MOP:0002192
+ has_participant: CHEBI:18915
+ N-3-O-beta-D-galactosyl-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 3-O-beta-D-galactosyl-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ MOP:0002193
+ has_participant: CHEBI:18939
+ N-1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0002194
+ has_participant: CHEBI:17571
+ N-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0002195
+ has_participant: CHEBI:17785
+ N-alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0002196
+ has_participant: CHEBI:22381
+ N-alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminyl group.
+ MOP:0002197
+ has_participant: CHEBI:22779
+ N-beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0002198
+ has_participant: CHEBI:21580
+ N-N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0002199
+ has_participant: CHEBI:21581
+ N-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0002200
+ has_participant: CHEBI:21582
+ N-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0002201
+ has_participant: CHEBI:21583
+ N-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0002202
+ has_participant: CHEBI:16059
+ N-N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0002203
+ has_participant: CHEBI:16198
+ N-N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an iduronosyl group.
+ MOP:0002204
+ has_participant: CHEBI:24770
+ N-iduronosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an iduronosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-inosinyl group.
+ MOP:0002205
+ has_participant: CHEBI:24845
+ N-5'-inosinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-inosinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a mannosyl group.
+ MOP:0002209
+ MOP:0002206
+ has_participant: CHEBI:25171
+ N-mannosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a (N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ MOP:0002207
+ has_participant: CHEBI:18638
+ N-(N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a (N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-D-mannosyl-1,3-(r1)-beta-D-mannosyl group.
+ MOP:0002208
+ has_participant: CHEBI:22406
+ N-alpha-D-mannosyl-1,3-(r1)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-D-mannosyl-1,3-(r1)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-mannosyl group.
+ MOP:0002210
+ has_participant: CHEBI:30689
+ N-alpha-mannosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosyl group.
+ MOP:0002211
+ has_participant: CHEBI:32618
+ N-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosyl group.
+ MOP:0002212
+ has_participant: CHEBI:32890
+ N-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ MOP:0002213
+ has_participant: CHEBI:21589
+ N-N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosyl group.
+ MOP:0002214
+ has_participant: CHEBI:32601
+ N-N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosyl group.
+ MOP:0002215
+ has_participant: CHEBI:32602
+ N-N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-D-mannosyl-(1->3)-beta-D-mannosyl group.
+ MOP:0002216
+ has_participant: CHEBI:32591
+ N-alpha-D-mannosyl-(1->3)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-D-mannosyl-(1->3)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a neuraminosyl group.
+ MOP:0002217
+ has_participant: CHEBI:25509
+ N-neuraminosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a neuraminosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a neuraminoyl group.
+ MOP:0002218
+ has_participant: CHEBI:25510
+ N-neuraminoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a neuraminoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a ribosyl group.
+ MOP:0002221
+ MOP:0002219
+ has_participant: CHEBI:26566
+ N-ribosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a ribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an adenosinediphosphoribosyl group.
+ MOP:0002220
+ has_participant: CHEBI:22259
+ N-adenosinediphosphoribosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an adenosinediphosphoribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-deoxyribosyl group.
+ MOP:0002222
+ has_participant: CHEBI:30720
+ N-2-deoxyribosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-deoxyribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sialosyl group.
+ MOP:0002223
+ has_participant: CHEBI:26668
+ N-sialosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sialosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a hemicystyl group.
+ MOP:0002224
+ has_participant: CHEBI:24492
+ N-hemicystylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a hemicystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a mevalonoyl group.
+ MOP:0002225
+ has_participant: CHEBI:25353
+ N-mevalonoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a mevalonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a montanoyl group.
+ MOP:0002226
+ has_participant: CHEBI:25417
+ N-montanoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a montanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a muramyl group.
+ MOP:0002227
+ has_participant: CHEBI:25433
+ N-muramylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nucleotidyl group.
+ MOP:0002228
+ has_participant: CHEBI:25613
+ N-nucleotidylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nucleotidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-adenylyl group.
+ MOP:0002229
+ has_participant: CHEBI:22263
+ N-5'-adenylylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-adenylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-cytidylyl group.
+ MOP:0002230
+ has_participant: CHEBI:23526
+ N-5'-cytidylylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-cytidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-thymidylyl group.
+ MOP:0002231
+ has_participant: CHEBI:27003
+ N-5'-thymidylylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-thymidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-uridylyl group.
+ MOP:0002232
+ has_participant: CHEBI:27244
+ N-5'-uridylylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-uridylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-guanylyl group.
+ MOP:0002233
+ has_participant: CHEBI:24460
+ N-5'-guanylylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-guanylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-ribothymidylyl group.
+ MOP:0002234
+ has_participant: CHEBI:26569
+ N-5'-ribothymidylylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-ribothymidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-inosinylyl group.
+ MOP:0002235
+ has_participant: CHEBI:33512
+ N-5'-inosinylylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-inosinylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pantothenyl group.
+ MOP:0002236
+ has_participant: CHEBI:25850
+ N-pantothenylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pantothenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pantoyl group.
+ MOP:0002237
+ has_participant: CHEBI:25851
+ N-pantoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pantoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a peptidyl group.
+ MOP:0002238
+ has_participant: CHEBI:25907
+ N-peptidylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a peptidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phthalyl group.
+ MOP:0002239
+ has_participant: CHEBI:26096
+ N-phthalylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phthalyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a propionyl group.
+ MOP:0002240
+ has_participant: CHEBI:26294
+ N-propionylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a propionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pyruvoyl group.
+ MOP:0002241
+ has_participant: CHEBI:45360
+ N-pyruvoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pyruvoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a retinoyl group.
+ MOP:0002242
+ has_participant: CHEBI:26539
+ N-retinoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a retinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sialoyl group.
+ MOP:0002243
+ has_participant: CHEBI:26670
+ N-sialoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 3-carboxypropanoyl group.
+ MOP:0002244
+ has_participant: CHEBI:26810
+ N-3-carboxypropanoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 3-carboxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trienoyl group.
+ MOP:0002245
+ has_participant: CHEBI:27107
+ N-trienoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an anilinocarbonyl group.
+ MOP:0002246
+ has_participant: CHEBI:30692
+ N-anilinocarbonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an anilinocarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pteroyl group.
+ MOP:0002247
+ has_participant: CHEBI:26379
+ N-pteroylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pteroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 3-carboxyprop-2-enoyl group.
+ MOP:0002248
+ has_participant: CHEBI:37953
+ N-3-carboxyprop-2-enoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a (Z)-3-carboxyprop-2-enoyl group.
+ MOP:0002249
+ has_participant: CHEBI:25122
+ N-(Z)-3-carboxyprop-2-enoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a (Z)-3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a (E)-3-carboxyprop-2-enoyl group.
+ MOP:0002250
+ has_participant: CHEBI:24126
+ N-(E)-3-carboxyprop-2-enoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a (E)-3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2,6-dichlorobenzoyl group.
+ MOP:0002251
+ has_participant: CHEBI:48625
+ N-2,6-dichlorobenzoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2,6-dichlorobenzoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-muramyl group.
+ MOP:0002252
+ has_participant: CHEBI:30701
+ N-alpha-muramylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-muramyl group.
+ MOP:0002253
+ has_participant: CHEBI:30702
+ N-beta-muramylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a beta-muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a dihydrolipoyl group.
+ MOP:0002254
+ has_participant: CHEBI:50488
+ N-dihydrolipoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sinapoyl group.
+ MOP:0002255
+ has_participant: CHEBI:50561
+ N-sinapoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sinapoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carboxyacetyl group.
+ MOP:0002256
+ has_participant: CHEBI:50650
+ N-carboxyacetylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carboxyacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a divalent carboacyl group.
+ MOP:0002257
+ has_participant: CHEBI:23855
+ N-divalent carboacylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a divalent carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an aspartoyl group.
+ MOP:0002258
+ has_participant: CHEBI:22663
+ N-aspartoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-aspartoyl group.
+ MOP:0002259
+ has_participant: CHEBI:32464
+ N-L-aspartoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-aspartoyl group.
+ MOP:0002260
+ has_participant: CHEBI:32468
+ N-D-aspartoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a citraconoyl group.
+ MOP:0002261
+ has_participant: CHEBI:23315
+ N-citraconoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a citraconoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glutamoyl group.
+ MOP:0002262
+ has_participant: CHEBI:24322
+ N-glutamoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-glutamoyl group.
+ MOP:0002263
+ has_participant: CHEBI:32481
+ N-D-glutamoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-glutamoyl group.
+ MOP:0002264
+ has_participant: CHEBI:32475
+ N-L-glutamoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a maloyl group.
+ MOP:0002265
+ has_participant: CHEBI:25138
+ N-maloylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a maloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phthaloyl group.
+ MOP:0002266
+ has_participant: CHEBI:26095
+ N-phthaloylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phthaloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a succinyl group.
+ MOP:0002267
+ has_participant: CHEBI:37952
+ N-succinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a succinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a butenedioyl group.
+ MOP:0002268
+ has_participant: CHEBI:37954
+ N-butenedioylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a butenedioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a fumaroyl group.
+ MOP:0002269
+ has_participant: CHEBI:24125
+ N-fumaroylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a fumaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a maleoyl group.
+ MOP:0002270
+ has_participant: CHEBI:25121
+ N-maleoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a maleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a hexanedioyl group.
+ MOP:0002271
+ has_participant: CHEBI:48082
+ N-hexanedioylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a hexanedioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a malonyl group.
+ MOP:0002272
+ has_participant: CHEBI:25134
+ N-malonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a malonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an ornithyl group.
+ MOP:0002273
+ has_participant: CHEBI:46929
+ N-ornithylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an ornithyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-ornithyl group.
+ MOP:0002274
+ has_participant: CHEBI:44700
+ N-L-ornithylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-ornithyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a half-cystyl group.
+ MOP:0002275
+ has_participant: CHEBI:30770
+ N-half-cystylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a half-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-tyrosin-O(4)-yl group.
+ MOP:0002276
+ has_participant: CHEBI:32768
+ N-L-tyrosin-O(4)-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-threonin-O(3)-yl group.
+ MOP:0002277
+ has_participant: CHEBI:32825
+ N-L-threonin-O(3)-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an L-threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-tyrosin-O(4)-yl group.
+ MOP:0002278
+ has_participant: CHEBI:32780
+ N-D-tyrosin-O(4)-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-threonin-O(3)-yl group.
+ MOP:0002279
+ has_participant: CHEBI:32831
+ N-D-threonin-O(3)-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a D-threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tyrosin-O(4)-yl group.
+ MOP:0002280
+ has_participant: CHEBI:32788
+ N-tyrosin-O(4)-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a threonin-O(3)-yl group.
+ MOP:0002281
+ has_participant: CHEBI:26985
+ N-threonin-O(3)-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an oxalyl group.
+ MOP:0002282
+ has_participant: CHEBI:30870
+ N-oxalylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an oxalyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a fumagillin-2-yl group.
+ MOP:0002283
+ has_participant: CHEBI:42601
+ N-fumagillin-2-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a fumagillin-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acetoacetyl group.
+ MOP:0002284
+ has_participant: CHEBI:48051
+ N-acetoacetylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acetoacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-linolenoyl group.
+ MOP:0002285
+ has_participant: CHEBI:32388
+ N-alpha-linolenoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alpha-linolenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a gamma-linolenoyl group.
+ MOP:0002286
+ has_participant: CHEBI:32390
+ N-gamma-linolenoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a gamma-linolenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carbamimidoyl group.
+ MOP:0002287
+ has_participant: CHEBI:48090
+ N-carbamimidoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carbamimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a formimidoyl group.
+ MOP:0002288
+ has_participant: CHEBI:24084
+ N-formimidoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a formimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trifluoroacetyl group.
+ MOP:0002289
+ has_participant: CHEBI:45888
+ N-trifluoroacetylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trifluoroacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carboxymethyl group.
+ MOP:0002290
+ has_participant: CHEBI:41402
+ N-carboxymethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carboxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a methylenecarbonyl group.
+ MOP:0002291
+ has_participant: CHEBI:43923
+ N-methylenecarbonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a methylenecarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-hydroxyacetimidoyl group.
+ MOP:0002292
+ has_participant: CHEBI:48055
+ N-N-hydroxyacetimidoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-hydroxyacetimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acryloyl group.
+ MOP:0002293
+ has_participant: CHEBI:48077
+ N-acryloylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acryloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tert-butoxycarbonyl group.
+ MOP:0002294
+ has_participant: CHEBI:48502
+ N-tert-butoxycarbonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tert-butoxycarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfanediyl group.
+ MOP:0002295
+ has_participant: CHEBI:29830
+ N-sulfanediylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phenylsulfanyl group.
+ MOP:0002296
+ has_participant: CHEBI:48499
+ N-phenylsulfanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phenylsulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a methylsulfanyl group.
+ MOP:0002297
+ has_participant: CHEBI:48563
+ N-methylsulfanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a methylsulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfaniumyl group.
+ MOP:0002298
+ has_participant: CHEBI:36945
+ N-sulfaniumylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a disulfanidyl group.
+ MOP:0002299
+ has_participant: CHEBI:29838
+ N-disulfanidylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a disulfanidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a disulfanediyl group.
+ MOP:0002300
+ has_participant: CHEBI:29826
+ N-disulfanediylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a disulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a disulfanyl group.
+ MOP:0002301
+ has_participant: CHEBI:30605
+ N-disulfanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a disulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tetrasulfanyl group.
+ MOP:0002302
+ has_participant: CHEBI:30607
+ N-tetrasulfanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tetrasulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tetrasulfanediyl group.
+ MOP:0002303
+ has_participant: CHEBI:29836
+ N-tetrasulfanediylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tetrasulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trisulfanyl group.
+ MOP:0002304
+ has_participant: CHEBI:30606
+ N-trisulfanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trisulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trisulfanediyl group.
+ MOP:0002305
+ has_participant: CHEBI:29834
+ N-trisulfanediylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trisulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pentasulfanyl group.
+ MOP:0002306
+ has_participant: CHEBI:30608
+ N-pentasulfanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pentasulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a diselanyl group.
+ MOP:0002307
+ has_participant: CHEBI:30602
+ N-diselanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a diselanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tellanyl group.
+ MOP:0002308
+ has_participant: CHEBI:30458
+ N-tellanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tellanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tellanediyl group.
+ MOP:0002309
+ has_participant: CHEBI:30455
+ N-tellanediylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tellanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tellaniumyl group.
+ MOP:0002310
+ has_participant: CHEBI:30447
+ N-tellaniumylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tellaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a ditellanyl group.
+ MOP:0002311
+ has_participant: CHEBI:30601
+ N-ditellanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a ditellanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an amidyl group.
+ MOP:0002312
+ has_participant: CHEBI:48373
+ N-amidylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an amidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an azanediyl group.
+ MOP:0002313
+ has_participant: CHEBI:29343
+ N-azanediylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an azanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-aminoethyl group.
+ MOP:0002314
+ has_participant: CHEBI:22502
+ N-2-aminoethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-aminoethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 4-aminobutyl group.
+ MOP:0002315
+ has_participant: CHEBI:50339
+ N-4-aminobutylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 4-aminobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an azanetriyl group.
+ MOP:0002316
+ has_participant: CHEBI:30228
+ N-azanetriylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an azanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a hydrazine-1,2-diyl group.
+ MOP:0002317
+ has_participant: CHEBI:30098
+ N-hydrazine-1,2-diylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a hydrazine-1,2-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a diazyn-1-ium-1-yl group.
+ MOP:0002318
+ has_participant: CHEBI:30108
+ N-diazyn-1-ium-1-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a diazyn-1-ium-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phosphanetriyl group.
+ MOP:0002319
+ has_participant: CHEBI:30206
+ N-phosphanetriylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phosphanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phosphanediyl group.
+ MOP:0002320
+ has_participant: CHEBI:29944
+ N-phosphanediylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phosphanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phosphanyl group.
+ MOP:0002321
+ has_participant: CHEBI:29936
+ N-phosphanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phosphanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a lambda(5)-phosphanyl group.
+ MOP:0002322
+ has_participant: CHEBI:30284
+ N-lambda(5)-phosphanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a lambda(5)-phosphanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phosphaniumyl group.
+ MOP:0002323
+ has_participant: CHEBI:30279
+ N-phosphaniumylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phosphaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arsanyl group.
+ MOP:0002324
+ has_participant: CHEBI:29759
+ N-arsanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arsanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arsanediyl group.
+ MOP:0002325
+ has_participant: CHEBI:29763
+ N-arsanediylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arsanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arsanetriyl group.
+ MOP:0002326
+ has_participant: CHEBI:29766
+ N-arsanetriylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arsanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arsaniumyl group.
+ MOP:0002327
+ has_participant: CHEBI:29842
+ N-arsaniumylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arsaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a lambda(5)-arsanyl group.
+ MOP:0002328
+ has_participant: CHEBI:30273
+ N-lambda(5)-arsanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a lambda(5)-arsanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a stibaniumyl group.
+ MOP:0002329
+ has_participant: CHEBI:30291
+ N-stibaniumylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a stibaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a lambda(5)-stibanyl group.
+ MOP:0002330
+ has_participant: CHEBI:30293
+ N-lambda(5)-stibanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a lambda(5)-stibanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a boranyl group.
+ MOP:0002331
+ has_participant: CHEBI:33604
+ N-boranylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a boranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a boranetriyl group.
+ MOP:0002332
+ has_participant: CHEBI:30169
+ N-boranetriylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a boranetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a boranediyl group.
+ MOP:0002333
+ has_participant: CHEBI:38988
+ N-boranediylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a boranediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a boranuidyl group.
+ MOP:0002334
+ has_participant: CHEBI:30159
+ N-boranuidylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a boranuidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a germyl group.
+ MOP:0002335
+ has_participant: CHEBI:30542
+ N-germylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a germyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a germanediyl group.
+ MOP:0002336
+ has_participant: CHEBI:30554
+ N-germanediylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a germanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a germanetetrayl group.
+ MOP:0002337
+ has_participant: CHEBI:30547
+ N-germanetetraylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a germanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a germanetriyl group.
+ MOP:0002338
+ has_participant: CHEBI:30544
+ N-germanetriylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a germanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a silyl group.
+ MOP:0002339
+ has_participant: CHEBI:30541
+ N-silylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a silyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a silanediyl group.
+ MOP:0002340
+ has_participant: CHEBI:30587
+ N-silanediylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a silanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a silanetriyl group.
+ MOP:0002341
+ has_participant: CHEBI:30576
+ N-silanetriylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a silanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a silanetetrayl group.
+ MOP:0002342
+ has_participant: CHEBI:30583
+ N-silanetetraylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a silanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a disilanyl group.
+ MOP:0002343
+ has_participant: CHEBI:30594
+ N-disilanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a disilanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alumanyl group.
+ MOP:0002344
+ has_participant: CHEBI:30135
+ N-alumanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alumanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a stannyl group.
+ MOP:0002345
+ has_participant: CHEBI:30540
+ N-stannylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a stannyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a stannanetriyl group.
+ MOP:0002346
+ has_participant: CHEBI:30575
+ N-stannanetriylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a stannanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a plumbanetriyl group.
+ MOP:0002347
+ has_participant: CHEBI:30577
+ N-plumbanetriylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a plumbanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a plumbyl group.
+ MOP:0002348
+ has_participant: CHEBI:30543
+ N-plumbylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a plumbyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a gallanyl group.
+ MOP:0002349
+ has_participant: CHEBI:37119
+ N-gallanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a gallanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an indiganyl group.
+ MOP:0002350
+ has_participant: CHEBI:30431
+ N-indiganylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an indiganyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a thallanyl group.
+ MOP:0002351
+ has_participant: CHEBI:30442
+ N-thallanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a thallanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phosphatidyl group.
+ MOP:0002352
+ has_participant: CHEBI:26025
+ N-phosphatidylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phosphatidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nucleosidyl group.
+ MOP:0002353
+ has_participant: CHEBI:33494
+ N-nucleosidylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nucleosidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a guanosyl group.
+ MOP:0002354
+ has_participant: CHEBI:24459
+ N-guanosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a guanosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an inosyl group.
+ MOP:0002355
+ has_participant: CHEBI:24849
+ N-inosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an inosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a thymidyl group.
+ MOP:0002356
+ has_participant: CHEBI:27002
+ N-thymidylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a thymidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an adenosyl group.
+ MOP:0002357
+ has_participant: CHEBI:33505
+ N-adenosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an adenosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-adenosyl group.
+ MOP:0002358
+ has_participant: CHEBI:22261
+ N-5'-adenosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 5'-adenosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an uridyl group.
+ MOP:0002359
+ has_participant: CHEBI:27243
+ N-uridylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an uridyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cytidyl group.
+ MOP:0002360
+ has_participant: CHEBI:23525
+ N-cytidylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cytidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a dolichyl group.
+ MOP:0002361
+ has_participant: CHEBI:23883
+ N-dolichylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a dolichyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-trans,6-trans-farnesyl group.
+ MOP:0002362
+ has_participant: CHEBI:36535
+ N-2-trans,6-trans-farnesylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-trans,6-trans-farnesyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a margaryl group.
+ MOP:0002363
+ has_participant: CHEBI:32925
+ N-margarylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a margaryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a methyl group.
+ MOP:0002364
+ has_participant: CHEBI:32875
+ N-methylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a methyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a methanetetrayl group.
+ MOP:0002365
+ has_participant: CHEBI:30039
+ N-methanetetraylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a methanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a methanetriyl group.
+ MOP:0002366
+ has_participant: CHEBI:29433
+ N-methanetriylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a methanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trichloromethyl group.
+ MOP:0002367
+ has_participant: CHEBI:30736
+ N-trichloromethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trichloromethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trifluoromethyl group.
+ MOP:0002368
+ has_participant: CHEBI:50127
+ N-trifluoromethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trifluoromethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alkyl group.
+ MOP:0002369
+ has_participant: CHEBI:22323
+ N-alkylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a butyl group.
+ MOP:0002370
+ has_participant: CHEBI:41264
+ N-butylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a ceryl group.
+ MOP:0002371
+ has_participant: CHEBI:23081
+ N-cerylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a ceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a decyl group.
+ MOP:0002372
+ has_participant: CHEBI:23580
+ N-decylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a decyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a dodecyl group.
+ MOP:0002373
+ has_participant: CHEBI:23870
+ N-dodecylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a dodecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a heptyl group.
+ MOP:0002374
+ has_participant: CHEBI:24526
+ N-heptylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a heptyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a hexyl group.
+ MOP:0002375
+ has_participant: CHEBI:24593
+ N-hexylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a hexyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a myricyl group.
+ MOP:0002376
+ has_participant: CHEBI:25453
+ N-myricylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a myricyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a myristyl group.
+ MOP:0002377
+ has_participant: CHEBI:25457
+ N-myristylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a myristyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nonyl group.
+ MOP:0002378
+ has_participant: CHEBI:25589
+ N-nonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an octyl group.
+ MOP:0002379
+ has_participant: CHEBI:25657
+ N-octylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an octyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a palmityl group.
+ MOP:0002380
+ has_participant: CHEBI:25842
+ N-palmitylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a palmityl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pentyl group.
+ MOP:0002381
+ has_participant: CHEBI:25902
+ N-pentylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a propyl group.
+ MOP:0002382
+ has_participant: CHEBI:26308
+ N-propylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a propyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a stearyl group.
+ MOP:0002383
+ has_participant: CHEBI:26755
+ N-stearylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a stearyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an isopropyl group.
+ MOP:0002384
+ has_participant: CHEBI:30353
+ N-isopropylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an isopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an ethyl group.
+ MOP:0002385
+ has_participant: CHEBI:37807
+ N-ethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an ethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an isobutyl group.
+ MOP:0002386
+ has_participant: CHEBI:30356
+ N-isobutylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an isobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pentan-2-yl group.
+ MOP:0002387
+ has_participant: CHEBI:32880
+ N-pentan-2-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pentan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an isopentyl group.
+ MOP:0002388
+ has_participant: CHEBI:30359
+ N-isopentylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an isopentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 3-methylbutan-2-yl group.
+ MOP:0002389
+ has_participant: CHEBI:32882
+ N-3-methylbutan-2-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 3-methylbutan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tert-pentyl group.
+ MOP:0002390
+ has_participant: CHEBI:30360
+ N-tert-pentylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tert-pentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a neopentyl group.
+ MOP:0002391
+ has_participant: CHEBI:30357
+ N-neopentylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a neopentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an undecyl group.
+ MOP:0002392
+ has_participant: CHEBI:32900
+ N-undecylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an undecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tridecyl group.
+ MOP:0002393
+ has_participant: CHEBI:32908
+ N-tridecylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tridecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pentadecyl group.
+ MOP:0002394
+ has_participant: CHEBI:32909
+ N-pentadecylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pentadecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nonadecyl group.
+ MOP:0002395
+ has_participant: CHEBI:32928
+ N-nonadecylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nonadecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arachidyl group.
+ MOP:0002396
+ has_participant: CHEBI:32930
+ N-arachidylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arachidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a henicosyl group.
+ MOP:0002397
+ has_participant: CHEBI:32932
+ N-henicosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a henicosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a behenyl group.
+ MOP:0002398
+ has_participant: CHEBI:32933
+ N-behenylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a behenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tricosyl group.
+ MOP:0002399
+ has_participant: CHEBI:32935
+ N-tricosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tricosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a lignoceryl group.
+ MOP:0002400
+ has_participant: CHEBI:32937
+ N-lignocerylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a lignoceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pentacosyl group.
+ MOP:0002401
+ has_participant: CHEBI:32939
+ N-pentacosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pentacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a heptacosyl group.
+ MOP:0002402
+ has_participant: CHEBI:32942
+ N-heptacosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a heptacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a montanyl group.
+ MOP:0002403
+ has_participant: CHEBI:32944
+ N-montanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a montanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nonacosyl group.
+ MOP:0002404
+ has_participant: CHEBI:32945
+ N-nonacosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nonacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sec-butyl group.
+ MOP:0002405
+ has_participant: CHEBI:45557
+ N-sec-butylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sec-butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tert-butyl group.
+ MOP:0002406
+ has_participant: CHEBI:30355
+ N-tert-butylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tert-butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pentan-3-yl group.
+ MOP:0002407
+ has_participant: CHEBI:32881
+ N-pentan-3-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a pentan-3-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-chloroethyl group.
+ MOP:0002408
+ has_participant: CHEBI:47553
+ N-2-chloroethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-chloroethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 1-chloroethyl group.
+ MOP:0002409
+ has_participant: CHEBI:48099
+ N-1-chloroethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 1-chloroethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a hydrocarbyl group.
+ MOP:0002410
+ has_participant: CHEBI:33248
+ N-hydrocarbylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a hydrocarbyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an aryl group.
+ MOP:0002411
+ has_participant: CHEBI:33338
+ N-arylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an aryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phenyl group.
+ MOP:0002412
+ has_participant: CHEBI:30396
+ N-phenylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a biphenyl-4-yl group.
+ MOP:0002413
+ has_participant: CHEBI:35447
+ N-biphenyl-4-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a biphenyl-4-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a naphthyl group.
+ MOP:0002414
+ has_participant: CHEBI:51140
+ N-naphthylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 1-naphthyl group.
+ MOP:0002415
+ has_participant: CHEBI:51138
+ N-1-naphthylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 1-naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-naphthyl group.
+ MOP:0002416
+ has_participant: CHEBI:51139
+ N-2-naphthylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cycloalkyl group.
+ MOP:0002417
+ has_participant: CHEBI:33441
+ N-cycloalkylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cycloalkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cyclobutyl group.
+ MOP:0002418
+ has_participant: CHEBI:30376
+ N-cyclobutylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cyclobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cyclopropyl group.
+ MOP:0002419
+ has_participant: CHEBI:30364
+ N-cyclopropylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cyclopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alkenyl group.
+ MOP:0002420
+ has_participant: CHEBI:37614
+ N-alkenylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alkenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an oleyl group.
+ MOP:0002421
+ has_participant: CHEBI:25670
+ N-oleylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an oleyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an allyl group.
+ MOP:0002422
+ has_participant: CHEBI:30361
+ N-allylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an allyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an isopropenyl group.
+ MOP:0002423
+ has_participant: CHEBI:30354
+ N-isopropenylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an isopropenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a vinyl group.
+ MOP:0002424
+ has_participant: CHEBI:37603
+ N-vinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a vinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a prenyl group.
+ MOP:0002427
+ MOP:0002425
+ has_participant: CHEBI:26248
+ N-prenylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a prenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phytyl group.
+ MOP:0002426
+ has_participant: CHEBI:26126
+ N-phytylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phytyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a polyprenyl group.
+ MOP:0002428
+ has_participant: CHEBI:26201
+ N-polyprenylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a polyprenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a farnesyl group.
+ MOP:0002429
+ has_participant: CHEBI:24017
+ N-farnesylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a farnesyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a geranyl group.
+ MOP:0002430
+ has_participant: CHEBI:24224
+ N-geranylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a geranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a geranylgeranyl group.
+ MOP:0002431
+ has_participant: CHEBI:24231
+ N-geranylgeranylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a geranylgeranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a retinyl group.
+ MOP:0002432
+ has_participant: CHEBI:26541
+ N-retinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a retinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an adamantan-2-yl group.
+ MOP:0002433
+ has_participant: CHEBI:48078
+ N-adamantan-2-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an adamantan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cycloalkenyl group.
+ MOP:0002434
+ has_participant: CHEBI:48886
+ N-cycloalkenylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cycloalkenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a campholenic cyclohexenyl group.
+ MOP:0002435
+ has_participant: CHEBI:48885
+ N-campholenic cyclohexenylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a campholenic cyclohexenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cyclopentadienyl group.
+ MOP:0002436
+ has_participant: CHEBI:30663
+ N-cyclopentadienylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an eta(5)-cyclopentadienyl group.
+ MOP:0002437
+ has_participant: CHEBI:36763
+ N-eta(5)-cyclopentadienylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an eta(5)-cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an eta(1)-cyclopentadienyl group.
+ MOP:0002438
+ has_participant: CHEBI:36764
+ N-eta(1)-cyclopentadienylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an eta(1)-cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an ethene-1,2-diyl group.
+ MOP:0002439
+ has_participant: CHEBI:46880
+ N-ethene-1,2-diylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an ethene-1,2-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arachidonyl group.
+ MOP:0002440
+ has_participant: CHEBI:22612
+ N-arachidonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arachidonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a benzyl group.
+ MOP:0002441
+ has_participant: CHEBI:22744
+ N-benzylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a benzyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an anthracen-1-yl group.
+ MOP:0002442
+ has_participant: CHEBI:48287
+ N-anthracen-1-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an anthracen-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an anthracen-2-yl group.
+ MOP:0002443
+ has_participant: CHEBI:48371
+ N-anthracen-2-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an anthracen-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an imidazolyl group.
+ MOP:0002444
+ has_participant: CHEBI:50052
+ N-imidazolylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an imidazolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an imidazol-1-yl group.
+ MOP:0002445
+ has_participant: CHEBI:50053
+ N-imidazol-1-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an imidazol-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an imidazol-2-yl group.
+ MOP:0002446
+ has_participant: CHEBI:50054
+ N-imidazol-2-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an imidazol-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an imidazol-5-yl group.
+ MOP:0002447
+ has_participant: CHEBI:50055
+ N-imidazol-5-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an imidazol-5-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an imidazol-4-yl group.
+ MOP:0002448
+ has_participant: CHEBI:50056
+ N-imidazol-4-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an imidazol-4-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a furyl group.
+ MOP:0002449
+ has_participant: CHEBI:24131
+ N-furylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-furyl group.
+ MOP:0002450
+ has_participant: CHEBI:19586
+ N-2-furylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 3-furyl group.
+ MOP:0002451
+ has_participant: CHEBI:20025
+ N-3-furylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 3-furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a thienyl group.
+ MOP:0002452
+ has_participant: CHEBI:37991
+ N-thienylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-thienyl group.
+ MOP:0002453
+ has_participant: CHEBI:35849
+ N-2-thienylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 3-thienyl group.
+ MOP:0002454
+ has_participant: CHEBI:37992
+ N-3-thienylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 3-thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an adenin-9-yl group.
+ MOP:0002455
+ has_participant: CHEBI:30756
+ N-adenin-9-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an adenin-9-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a guanin-9-yl group.
+ MOP:0002456
+ has_participant: CHEBI:30755
+ N-guanin-9-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a guanin-9-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acetimidoyl group.
+ MOP:0002457
+ has_participant: CHEBI:48050
+ N-acetimidoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acetimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an organyl group.
+ MOP:0002458
+ has_participant: CHEBI:33249
+ N-organylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an organyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an organic heterocyclyl group.
+ MOP:0002459
+ has_participant: CHEBI:33453
+ N-organic heterocyclylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an organic heterocyclyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a heteroaryl group.
+ MOP:0002460
+ has_participant: CHEBI:33470
+ N-heteroarylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a heteroaryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 4,4'-dimethoxytriphenylmethyl group.
+ MOP:0002461
+ has_participant: CHEBI:51095
+ N-4,4'-dimethoxytriphenylmethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 4,4'-dimethoxytriphenylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tauryl group.
+ MOP:0002462
+ has_participant: CHEBI:26861
+ N-taurylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tauryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a triflyl group.
+ MOP:0002463
+ has_participant: CHEBI:48548
+ N-triflylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a triflyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glycidyl group.
+ MOP:0002464
+ has_participant: CHEBI:24366
+ N-glycidylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a glycidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfanylmethyl group.
+ MOP:0002465
+ has_participant: CHEBI:50326
+ N-sulfanylmethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfanylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a selanylmethyl group.
+ MOP:0002466
+ has_participant: CHEBI:50327
+ N-selanylmethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a selanylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-carboxyethyl group.
+ MOP:0002467
+ has_participant: CHEBI:50329
+ N-2-carboxyethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-carboxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-amino-2-oxoethyl group.
+ MOP:0002468
+ has_participant: CHEBI:50330
+ N-2-amino-2-oxoethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-amino-2-oxoethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 3-amino-3-oxopropyl group.
+ MOP:0002469
+ has_participant: CHEBI:50331
+ N-3-amino-3-oxopropylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 3-amino-3-oxopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-(methylsulfanyl)ethyl group.
+ MOP:0002470
+ has_participant: CHEBI:50332
+ N-2-(methylsulfanyl)ethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-(methylsulfanyl)ethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 4-hydroxybenzyl group.
+ MOP:0002471
+ has_participant: CHEBI:50336
+ N-4-hydroxybenzylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 4-hydroxybenzyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 1H-indol-3-ylmethyl group.
+ MOP:0002472
+ has_participant: CHEBI:50337
+ N-1H-indol-3-ylmethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 1H-indol-3-ylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 1H-imidazol-4-ylmethyl group.
+ MOP:0002473
+ has_participant: CHEBI:50338
+ N-1H-imidazol-4-ylmethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 1H-imidazol-4-ylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 3-carbamimidamidopropyl group.
+ MOP:0002474
+ has_participant: CHEBI:50340
+ N-3-carbamimidamidopropylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 3-carbamimidamidopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a hydroxymethyl group.
+ MOP:0002475
+ has_participant: CHEBI:24712
+ N-hydroxymethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a hydroxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 1-hydroxyethyl group.
+ MOP:0002476
+ has_participant: CHEBI:50341
+ N-1-hydroxyethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 1-hydroxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a haloalkyl group.
+ MOP:0002477
+ has_participant: CHEBI:50491
+ N-haloalkylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a haloalkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-(trimethylsilyl)ethoxymethyl group.
+ MOP:0002478
+ has_participant: CHEBI:51093
+ N-2-(trimethylsilyl)ethoxymethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-(trimethylsilyl)ethoxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acyl group.
+ MOP:0002479
+ has_participant: CHEBI:22221
+ N-acylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an organoheteryl group.
+ MOP:0002480
+ has_participant: CHEBI:33456
+ N-organoheterylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an organoheteryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an oxalosulfanyl group.
+ MOP:0002481
+ has_participant: CHEBI:30874
+ N-oxalosulfanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an oxalosulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an organosilyl group.
+ MOP:0002482
+ has_participant: CHEBI:33478
+ N-organosilylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an organosilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trimethylsilyl group.
+ MOP:0002483
+ has_participant: CHEBI:51088
+ N-trimethylsilylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trimethylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a triisopropylsilyl group.
+ MOP:0002484
+ has_participant: CHEBI:51089
+ N-triisopropylsilylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a triisopropylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tert-butyldiphenylsilyl group.
+ MOP:0002485
+ has_participant: CHEBI:51090
+ N-tert-butyldiphenylsilylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tert-butyldiphenylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tert-butyldimethylsilyl group.
+ MOP:0002486
+ has_participant: CHEBI:51091
+ N-tert-butyldimethylsilylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tert-butyldimethylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a thioacyl group.
+ MOP:0002487
+ has_participant: CHEBI:49063
+ N-thioacylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a thioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carbothioacyl group.
+ MOP:0002488
+ has_participant: CHEBI:49066
+ N-carbothioacylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an univalent carbothioacyl group.
+ MOP:0002489
+ has_participant: CHEBI:49067
+ N-univalent carbothioacylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an univalent carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a divalent carbothioacyl group.
+ MOP:0002490
+ has_participant: CHEBI:49068
+ N-divalent carbothioacylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a divalent carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carbonimidoyl group.
+ MOP:0002491
+ has_participant: CHEBI:29815
+ N-carbonimidoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carbonimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a thiocarbonyl group.
+ MOP:0002492
+ has_participant: CHEBI:30256
+ N-thiocarbonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a thiocarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a (fluoren-9-ylmethoxy)carbonyl group.
+ MOP:0002493
+ has_participant: CHEBI:48605
+ N-(fluoren-9-ylmethoxy)carbonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a (fluoren-9-ylmethoxy)carbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carbonyl group.
+ MOP:0002494
+ has_participant: CHEBI:23019
+ N-carbonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a carbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cytosin-1-yl group.
+ MOP:0002495
+ has_participant: CHEBI:30758
+ N-cytosin-1-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a cytosin-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a thymin-1-yl group.
+ MOP:0002496
+ has_participant: CHEBI:30757
+ N-thymin-1-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a thymin-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an uracil-1-yl group.
+ MOP:0002497
+ has_participant: CHEBI:30759
+ N-uracil-1-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an uracil-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a morpholin-4-ylsulfonyl group.
+ MOP:0002498
+ has_participant: CHEBI:45701
+ N-morpholin-4-ylsulfonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a morpholin-4-ylsulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acetohydrazonoyl group.
+ MOP:0002499
+ has_participant: CHEBI:48054
+ N-acetohydrazonoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acetohydrazonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-hydroxyethyl group.
+ MOP:0002500
+ has_participant: CHEBI:44730
+ N-2-hydroxyethylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a 2-hydroxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an aminosulfinyl group.
+ MOP:0002501
+ has_participant: CHEBI:48257
+ N-aminosulfinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an aminosulfinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a disiloxanyl group.
+ MOP:0002502
+ has_participant: CHEBI:48142
+ N-disiloxanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a disiloxanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a disiloxane-1,3-diyl group.
+ MOP:0002503
+ has_participant: CHEBI:48143
+ N-disiloxane-1,3-diylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a disiloxane-1,3-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an azinoyl group.
+ MOP:0002504
+ has_participant: CHEBI:29771
+ N-azinoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an azinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an azonoyl group.
+ MOP:0002505
+ has_participant: CHEBI:37768
+ N-azonoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an azonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phosphorothioyl group.
+ MOP:0002506
+ has_participant: CHEBI:32412
+ N-phosphorothioylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phosphorothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phosphonothioyl group.
+ MOP:0002507
+ has_participant: CHEBI:32413
+ N-phosphonothioylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phosphonothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arsonoyl group.
+ MOP:0002508
+ has_participant: CHEBI:29848
+ N-arsonoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arsonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arsinoyl group.
+ MOP:0002509
+ has_participant: CHEBI:30277
+ N-arsinoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arsinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a stiboryl group.
+ MOP:0002510
+ has_participant: CHEBI:48439
+ N-stiborylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a stiboryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfamoyl group.
+ MOP:0002511
+ has_participant: CHEBI:48266
+ N-sulfamoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a S-aminosulfinimidoyl group.
+ MOP:0002512
+ has_participant: CHEBI:48254
+ N-S-aminosulfinimidoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a S-aminosulfinimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a S-aminosulfonimidoyl group.
+ MOP:0002513
+ has_participant: CHEBI:48264
+ N-S-aminosulfonimidoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a S-aminosulfonimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a chloryl group.
+ MOP:0002514
+ has_participant: CHEBI:29883
+ N-chlorylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a chloryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a chlorosyl group.
+ MOP:0002515
+ has_participant: CHEBI:29878
+ N-chlorosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a chlorosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a perchloryl group.
+ MOP:0002516
+ has_participant: CHEBI:29877
+ N-perchlorylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a perchloryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a bromosyl group.
+ MOP:0002517
+ has_participant: CHEBI:29871
+ N-bromosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a bromosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a bromyl group.
+ MOP:0002518
+ has_participant: CHEBI:29881
+ N-bromylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a bromyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a perbromyl group.
+ MOP:0002519
+ has_participant: CHEBI:29891
+ N-perbromylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a perbromyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an iodosyl group.
+ MOP:0002520
+ has_participant: CHEBI:29897
+ N-iodosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an iodosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an iodyl group.
+ MOP:0002521
+ has_participant: CHEBI:29904
+ N-iodylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an iodyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a periodyl group.
+ MOP:0002522
+ has_participant: CHEBI:29908
+ N-periodylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a periodyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a fluorosyl group.
+ MOP:0002523
+ has_participant: CHEBI:30241
+ N-fluorosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a fluorosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfonyl group.
+ MOP:0002539
+ MOP:0002524
+ has_participant: CHEBI:29825
+ N-sulfonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acetoxysulfonyl group.
+ MOP:0002525
+ has_participant: CHEBI:48065
+ N-acetoxysulfonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acetoxysulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfonothioyl group.
+ MOP:0002526
+ has_participant: CHEBI:29828
+ N-sulfonothioylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfonothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfinothioyl group.
+ MOP:0002527
+ has_participant: CHEBI:29827
+ N-sulfinothioylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfinothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfonodithioyl group.
+ MOP:0002528
+ has_participant: CHEBI:29835
+ N-sulfonodithioylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfonodithioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trioxidanyl group.
+ MOP:0002529
+ has_participant: CHEBI:29791
+ N-trioxidanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trioxidanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trioxidanediyl group.
+ MOP:0002530
+ has_participant: CHEBI:30493
+ N-trioxidanediylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a trioxidanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a heterocyclyl group.
+ MOP:0002531
+ has_participant: CHEBI:48271
+ N-heterocyclylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a heterocyclyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phosphoramidochloridoyl group.
+ MOP:0002532
+ has_participant: CHEBI:48229
+ N-phosphoramidochloridoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a phosphoramidochloridoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a S-aminosulfonodiimidoyl group.
+ MOP:0002533
+ has_participant: CHEBI:48265
+ N-S-aminosulfonodiimidoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a S-aminosulfonodiimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an aminosulfanyl group.
+ MOP:0002534
+ has_participant: CHEBI:48252
+ N-aminosulfanylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an aminosulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfinyl group.
+ MOP:0002535
+ has_participant: CHEBI:29822
+ N-sulfinylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arsoryl group.
+ MOP:0002536
+ has_participant: CHEBI:30274
+ N-arsorylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an arsoryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an azanediidyl group.
+ MOP:0002537
+ has_participant: CHEBI:30227
+ N-azanediidylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an azanediidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfinimidoyl group.
+ MOP:0002538
+ has_participant: CHEBI:29829
+ N-sulfinimidoylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfinimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tosyl group.
+ MOP:0002540
+ has_participant: CHEBI:51094
+ N-tosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a tosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a brosyl group.
+ MOP:0002541
+ has_participant: CHEBI:51101
+ N-brosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a brosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nosyl group.
+ MOP:0002542
+ has_participant: CHEBI:51102
+ N-nosylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an indolyl group.
+ MOP:0002544
+ has_participant: CHEBI:51609
+ N-indolylamination
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an indolyl group.
+ RSC:xp
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an indol-1-yl group.
+ MOP:0002545
+ has_participant: CHEBI:51610
+ N-indol-1-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an indol-1-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an indol-2-yl group.
+ MOP:0002546
+ has_participant: CHEBI:51611
+ N-indol-2-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an indol-2-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an indol-3-yl group.
+ MOP:0002547
+ has_participant: CHEBI:51612
+ N-indol-3-ylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an indol-3-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-oxindolyl group.
+ MOP:0002548
+ has_participant: CHEBI:51613
+ N-N-oxindolylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an N-oxindolyl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alkylamino group.
+ MOP:0002549
+ has_participant: CHEBI:22332
+ N-alkylamination
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alkylamino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a halo group.
+ MOP:0002550
+ has_participant: CHEBI:47854
+ N-halogenation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a halo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a bromo group.
+ MOP:0002551
+ has_participant: CHEBI:47265
+ N-bromination
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a bromo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a chloro group.
+ MOP:0002552
+ has_participant: CHEBI:47853
+ N-chlorination
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a chloro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a fluoro group.
+ MOP:0002553
+ has_participant: CHEBI:42645
+ N-fluorination
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a fluoro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an iodo group.
+ MOP:0002554
+ has_participant: CHEBI:43448
+ N-iodination
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an iodo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an imino group.
+ MOP:0002555
+ has_participant: CHEBI:29342
+ N-imination
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an imino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nitro group.
+ MOP:0002556
+ has_participant: CHEBI:29785
+ N-nitration
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a nitro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a hydroxyamino group.
+ MOP:0002557
+ has_participant: CHEBI:29769
+ N-hydroxyamination
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a hydroxyamino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a thioxo group.
+ MOP:0002558
+ has_participant: CHEBI:29833
+ N-thioxonation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a thioxo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfo group.
+ MOP:0002559
+ has_participant: CHEBI:29922
+ N-sulfonation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a selenono group.
+ MOP:0002560
+ has_participant: CHEBI:29923
+ N-selenonation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a selenono group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a boryl group (-BR'R').
+ MOP:0003000
+ Submitted to ChEBI
+ O-borylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a boryl group (-BR'R').
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a methanidyl group.
+ MOP:0003001
+ has_participant: CHEBI:29361
+ O-methanidylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a methanidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an azaniumyl group.
+ MOP:0003002
+ has_participant: CHEBI:48284
+ O-azaniumylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an azaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a formyl group.
+ MOP:0003003
+ has_participant: CHEBI:42485
+ O-formylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a formyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acetonyl group.
+ MOP:0003004
+ has_participant: CHEBI:48056
+ O-acetonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acetonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-cystyl group.
+ MOP:0003005
+ has_participant: CHEBI:50057
+ O-L-cystylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-cystinyl group.
+ MOP:0003006
+ has_participant: CHEBI:50066
+ O-L-cystinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-cystinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-cystyl group.
+ MOP:0003007
+ has_participant: CHEBI:50049
+ O-D-cystylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cystinyl group.
+ MOP:0003008
+ has_participant: CHEBI:50050
+ O-cystinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cystinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cystyl group.
+ MOP:0003009
+ has_participant: CHEBI:23514
+ O-cystylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cysteinyl group.
+ MOP:0003010
+ has_participant: CHEBI:23511
+ O-cysteinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-cysteinyl group.
+ MOP:0003011
+ has_participant: CHEBI:32447
+ O-L-cysteinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-cysteinyl group.
+ MOP:0003012
+ has_participant: CHEBI:32452
+ O-D-cysteinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cystein-S-yl group.
+ MOP:0003013
+ has_participant: CHEBI:32795
+ O-cystein-S-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-cystein-S-yl group.
+ MOP:0003014
+ has_participant: CHEBI:32794
+ O-D-cystein-S-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-cystein-S-yl group.
+ MOP:0003015
+ has_participant: CHEBI:32793
+ O-L-cystein-S-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a methionyl group.
+ MOP:0003016
+ has_participant: CHEBI:37902
+ O-methionylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-methionyl group.
+ MOP:0003017
+ has_participant: CHEBI:49038
+ O-L-methionylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-formyl-L-methionyl group.
+ MOP:0003018
+ has_participant: CHEBI:49298
+ O-N-formyl-L-methionylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-formyl-L-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-methionyl group.
+ MOP:0003019
+ has_participant: CHEBI:32640
+ O-D-methionylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an (R)-lipoyl group.
+ MOP:0003020
+ has_participant: CHEBI:38232
+ O-(R)-lipoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an (R)-lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an (S)-lipoyl group.
+ MOP:0003021
+ has_participant: CHEBI:38233
+ O-(S)-lipoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an (S)-lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a lipoyl group.
+ MOP:0003022
+ has_participant: CHEBI:25064
+ O-lipoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an (R)-dihydrolipoyl group.
+ MOP:0003023
+ has_participant: CHEBI:30319
+ O-(R)-dihydrolipoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an (R)-dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an (S)-dihydrolipoyl group.
+ MOP:0003024
+ has_participant: CHEBI:50489
+ O-(S)-dihydrolipoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an (S)-dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-sialoyl group.
+ MOP:0003025
+ has_participant: CHEBI:32960
+ O-alpha-sialoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-sialoyl group.
+ MOP:0003026
+ has_participant: CHEBI:32961
+ O-beta-sialoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glyceroyl group.
+ MOP:0003027
+ has_participant: CHEBI:30750
+ O-glyceroylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glyceroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carboacyl group.
+ MOP:0003028
+ has_participant: CHEBI:37838
+ O-carboacylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an univalent carboacyl group.
+ MOP:0003029
+ has_participant: CHEBI:27207
+ O-univalent carboacylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an univalent carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acetyl group.
+ MOP:0003030
+ has_participant: CHEBI:40574
+ O-acetylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-aminoacyl group.
+ MOP:0003031
+ has_participant: CHEBI:22487
+ O-alpha-aminoacylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-aminoacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alanyl group.
+ MOP:0003032
+ has_participant: CHEBI:22280
+ O-alanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-alanyl group.
+ MOP:0003033
+ has_participant: CHEBI:32433
+ O-L-alanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-alanyl group.
+ MOP:0003034
+ has_participant: CHEBI:32437
+ O-D-alanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-aspartyl group.
+ MOP:0003035
+ has_participant: CHEBI:22445
+ O-alpha-aspartylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-alpha-aspartyl group.
+ MOP:0003036
+ has_participant: CHEBI:32462
+ O-L-alpha-aspartylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-alpha-aspartyl group.
+ MOP:0003037
+ has_participant: CHEBI:32466
+ O-D-alpha-aspartylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-glutamyl group.
+ MOP:0003038
+ has_participant: CHEBI:22453
+ O-alpha-glutamylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-alpha-glutamyl group.
+ MOP:0003039
+ has_participant: CHEBI:46855
+ O-L-alpha-glutamylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-alpha-glutamyl group.
+ MOP:0003040
+ has_participant: CHEBI:32479
+ O-D-alpha-glutamylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pteroylglutamyl group.
+ MOP:0003041
+ has_participant: CHEBI:26380
+ O-pteroylglutamylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pteroylglutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phenylalanyl group.
+ MOP:0003042
+ has_participant: CHEBI:25987
+ O-phenylalanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-phenylalanyl group.
+ MOP:0003043
+ has_participant: CHEBI:32496
+ O-L-phenylalanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-phenylalanyl group.
+ MOP:0003044
+ has_participant: CHEBI:32500
+ O-D-phenylalanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glycyl group.
+ MOP:0003045
+ has_participant: CHEBI:46740
+ O-glycylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glycyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a histidyl group.
+ MOP:0003046
+ has_participant: CHEBI:37906
+ O-histidylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-histidyl group.
+ MOP:0003047
+ has_participant: CHEBI:32514
+ O-L-histidylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-histidyl group.
+ MOP:0003048
+ has_participant: CHEBI:32522
+ O-D-histidylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an isoleucyl group.
+ MOP:0003049
+ has_participant: CHEBI:37905
+ O-isoleucylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-isoleucyl group.
+ MOP:0003050
+ has_participant: CHEBI:32606
+ O-L-isoleucylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-isoleucyl group.
+ MOP:0003051
+ has_participant: CHEBI:32610
+ O-D-isoleucylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a lysyl group.
+ MOP:0003052
+ has_participant: CHEBI:37903
+ O-lysylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-lysyl group.
+ MOP:0003053
+ has_participant: CHEBI:32553
+ O-L-lysylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a deoxyhypusinyl group.
+ MOP:0003054
+ has_participant: CHEBI:50039
+ O-deoxyhypusinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a deoxyhypusinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-lysyl group.
+ MOP:0003055
+ has_participant: CHEBI:32559
+ O-D-lysylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a leucyl group.
+ MOP:0003056
+ has_participant: CHEBI:37904
+ O-leucylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-leucyl group.
+ MOP:0003057
+ has_participant: CHEBI:32621
+ O-L-leucylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-leucyl group.
+ MOP:0003058
+ has_participant: CHEBI:32625
+ O-D-leucylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an asparaginyl group.
+ MOP:0003059
+ has_participant: CHEBI:22656
+ O-asparaginylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-asparaginyl group.
+ MOP:0003060
+ has_participant: CHEBI:50348
+ O-L-asparaginylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-asparaginyl group.
+ MOP:0003061
+ has_participant: CHEBI:32653
+ O-D-asparaginylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a prolyl group.
+ MOP:0003062
+ has_participant: CHEBI:26274
+ O-prolylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-prolyl group.
+ MOP:0003063
+ has_participant: CHEBI:32865
+ O-L-prolylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-prolyl group.
+ MOP:0003064
+ has_participant: CHEBI:32869
+ O-D-prolylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glutaminyl group.
+ MOP:0003065
+ has_participant: CHEBI:24320
+ O-glutaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-glutaminyl group.
+ MOP:0003066
+ has_participant: CHEBI:32667
+ O-L-glutaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-glutaminyl group.
+ MOP:0003067
+ has_participant: CHEBI:32674
+ O-D-glutaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a seryl group.
+ MOP:0003068
+ has_participant: CHEBI:37901
+ O-serylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-seryl group.
+ MOP:0003069
+ has_participant: CHEBI:32838
+ O-L-serylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-seryl group.
+ MOP:0003070
+ has_participant: CHEBI:32842
+ O-D-serylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a threonyl group.
+ MOP:0003071
+ has_participant: CHEBI:37900
+ O-threonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-threonyl group.
+ MOP:0003072
+ has_participant: CHEBI:32823
+ O-L-threonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-threonyl group.
+ MOP:0003073
+ has_participant: CHEBI:32829
+ O-D-threonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a selenocysteinyl group.
+ MOP:0003074
+ has_participant: CHEBI:32755
+ O-selenocysteinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-selenocysteinyl group.
+ MOP:0003075
+ has_participant: CHEBI:32745
+ O-L-selenocysteinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-selenocysteinyl group.
+ MOP:0003076
+ has_participant: CHEBI:32749
+ O-D-selenocysteinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a valyl group.
+ MOP:0003077
+ has_participant: CHEBI:37897
+ O-valylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-valyl group.
+ MOP:0003078
+ has_participant: CHEBI:32853
+ O-L-valylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-valyl group.
+ MOP:0003079
+ has_participant: CHEBI:32857
+ O-D-valylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tryptophyl group.
+ MOP:0003080
+ has_participant: CHEBI:37899
+ O-tryptophylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-tryptophyl group.
+ MOP:0003081
+ has_participant: CHEBI:32706
+ O-L-tryptophylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-tryptophyl group.
+ MOP:0003082
+ has_participant: CHEBI:32718
+ O-D-tryptophylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tyrosyl group.
+ MOP:0003083
+ has_participant: CHEBI:37898
+ O-tyrosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-tyrosyl group.
+ MOP:0003084
+ has_participant: CHEBI:32764
+ O-L-tyrosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-tyrosyl group.
+ MOP:0003085
+ has_participant: CHEBI:32778
+ O-D-tyrosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arginyl group.
+ MOP:0003086
+ has_participant: CHEBI:22619
+ O-arginylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-arginyl group.
+ MOP:0003087
+ has_participant: CHEBI:32684
+ O-L-arginylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-arginyl group.
+ MOP:0003088
+ has_participant: CHEBI:32691
+ O-D-arginylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a benzoyl group.
+ MOP:0003089
+ has_participant: CHEBI:22733
+ O-benzoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a benzoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-aspartyl group.
+ MOP:0003090
+ has_participant: CHEBI:22832
+ O-beta-aspartylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-beta-aspartyl group.
+ MOP:0003091
+ has_participant: CHEBI:32467
+ O-D-beta-aspartylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-beta-aspartyl group.
+ MOP:0003092
+ has_participant: CHEBI:48098
+ O-L-beta-aspartylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a biotinyl group.
+ MOP:0003093
+ has_participant: CHEBI:22885
+ O-biotinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a biotinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a butyryl group.
+ MOP:0003094
+ has_participant: CHEBI:22972
+ O-butyrylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a butyryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carbamoyl group.
+ MOP:0003095
+ has_participant: CHEBI:23004
+ O-carbamoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carbamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a C-aminocarbonohydrazonoyl group.
+ MOP:0003096
+ has_participant: CHEBI:48223
+ O-C-aminocarbonohydrazonoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a C-aminocarbonohydrazonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-(aminomethylidene)hydrazinyl group.
+ MOP:0003097
+ has_participant: CHEBI:48244
+ O-2-(aminomethylidene)hydrazinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-(aminomethylidene)hydrazinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carbamoylcarbamoyl group.
+ MOP:0003098
+ has_participant: CHEBI:48083
+ O-carbamoylcarbamoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carbamoylcarbamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carbamothioyl group.
+ MOP:0003099
+ has_participant: CHEBI:48225
+ O-carbamothioylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carbamothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acetylazanediyl group.
+ MOP:0003100
+ has_participant: CHEBI:48073
+ O-acetylazanediylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acetylazanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an oxamoyl group.
+ MOP:0003101
+ has_participant: CHEBI:48246
+ O-oxamoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an oxamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cholyl group.
+ MOP:0003102
+ has_participant: CHEBI:23220
+ O-cholylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cholyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an enoyl group.
+ MOP:0003103
+ has_participant: CHEBI:23916
+ O-enoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a fatty-acyl group.
+ MOP:0003104
+ has_participant: CHEBI:24027
+ O-fatty-acylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a fatty-acyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arachidonoyl group.
+ MOP:0003105
+ has_participant: CHEBI:22610
+ O-arachidonoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arachidonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arachidoyl group.
+ MOP:0003106
+ has_participant: CHEBI:22614
+ O-arachidoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arachidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a behenoyl group.
+ MOP:0003107
+ has_participant: CHEBI:22696
+ O-behenoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a behenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cerotoyl group.
+ MOP:0003108
+ has_participant: CHEBI:23080
+ O-cerotoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cerotoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a decanoyl group.
+ MOP:0003109
+ has_participant: CHEBI:23574
+ O-decanoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a decanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a dodecenoyl group.
+ MOP:0003110
+ has_participant: CHEBI:23868
+ O-dodecenoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a dodecenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an eleostearoyl group.
+ MOP:0003111
+ has_participant: CHEBI:23908
+ O-eleostearoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an eleostearoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a mycolyl group.
+ MOP:0003112
+ has_participant: CHEBI:25439
+ O-mycolylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a mycolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nervonoyl group.
+ MOP:0003113
+ has_participant: CHEBI:25503
+ O-nervonoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nervonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an octanoyl group.
+ MOP:0003114
+ has_participant: CHEBI:25650
+ O-octanoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an octanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a palmitoleoyl group.
+ MOP:0003115
+ has_participant: CHEBI:25837
+ O-palmitoleoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a palmitoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a palmitoyl group.
+ MOP:0003116
+ has_participant: CHEBI:45021
+ O-palmitoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a palmitoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a stearoyl group.
+ MOP:0003117
+ has_participant: CHEBI:26753
+ O-stearoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a stearoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an undecanoyl group.
+ MOP:0003118
+ has_participant: CHEBI:27190
+ O-undecanoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an undecanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a valeryl group.
+ MOP:0003119
+ has_participant: CHEBI:27265
+ O-valerylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a valeryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a hexanoyl group.
+ MOP:0003120
+ has_participant: CHEBI:24574
+ O-hexanoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a hexanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a heptanoyl group.
+ MOP:0003121
+ has_participant: CHEBI:32363
+ O-heptanoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a heptanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nonanoyl group.
+ MOP:0003122
+ has_participant: CHEBI:25580
+ O-nonanoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nonanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a lauroyl group.
+ MOP:0003123
+ has_participant: CHEBI:32359
+ O-lauroylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a lauroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a myristoyl group.
+ MOP:0003124
+ has_participant: CHEBI:25456
+ O-myristoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a myristoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a docosenoyl group.
+ MOP:0003125
+ has_participant: CHEBI:50479
+ O-docosenoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a docosenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cetoleoyl group.
+ MOP:0003126
+ has_participant: CHEBI:32430
+ O-cetoleoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cetoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an erucoyl group.
+ MOP:0003127
+ has_participant: CHEBI:32394
+ O-erucoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an erucoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an icosenoyl group.
+ MOP:0003128
+ has_participant: CHEBI:50480
+ O-icosenoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an icosenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a gadelaidoyl group.
+ MOP:0003129
+ has_participant: CHEBI:32424
+ O-gadelaidoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a gadelaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a gadoleoyl group.
+ MOP:0003130
+ has_participant: CHEBI:32421
+ O-gadoleoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a gadoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a gondoyl group.
+ MOP:0003131
+ has_participant: CHEBI:32427
+ O-gondoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a gondoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a heptatrienoyl group.
+ MOP:0003132
+ has_participant: CHEBI:50486
+ O-heptatrienoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a heptatrienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trans,trans-hepta-2,4,6-trienoyl group.
+ MOP:0003133
+ has_participant: CHEBI:30771
+ O-trans,trans-hepta-2,4,6-trienoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trans,trans-hepta-2,4,6-trienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an octadecenoyl group.
+ MOP:0003134
+ has_participant: CHEBI:50499
+ O-octadecenoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an octadecenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an octadec-6-enoyl group.
+ MOP:0003135
+ has_participant: CHEBI:50497
+ O-octadec-6-enoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an octadec-6-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a petroselaidoyl group.
+ MOP:0003136
+ has_participant: CHEBI:32378
+ O-petroselaidoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a petroselaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a petroselinoyl group.
+ MOP:0003137
+ has_participant: CHEBI:32376
+ O-petroselinoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a petroselinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a vaccenoyl group.
+ MOP:0003138
+ has_participant: CHEBI:27261
+ O-vaccenoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cis-vaccenoyl group.
+ MOP:0003139
+ has_participant: CHEBI:23313
+ O-cis-vaccenoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cis-vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trans-vaccenoyl group.
+ MOP:0003140
+ has_participant: CHEBI:27080
+ O-trans-vaccenoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trans-vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an octadec-9-enoyl group.
+ MOP:0003141
+ has_participant: CHEBI:50500
+ O-octadec-9-enoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an octadec-9-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an oleoyl group.
+ MOP:0003142
+ has_participant: CHEBI:25667
+ O-oleoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an oleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an elaidoyl group.
+ MOP:0003143
+ has_participant: CHEBI:23904
+ O-elaidoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an elaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a margaroyl group.
+ MOP:0003144
+ has_participant: CHEBI:32367
+ O-margaroylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a margaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a melissoyl group.
+ MOP:0003145
+ has_participant: CHEBI:31016
+ O-melissoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a melissoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a myristoleoyl group.
+ MOP:0003146
+ has_participant: CHEBI:32371
+ O-myristoleoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a myristoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an obtusiloyl group.
+ MOP:0003147
+ has_participant: CHEBI:33162
+ O-obtusiloylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an obtusiloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a lignoceroyl group.
+ MOP:0003148
+ has_participant: CHEBI:31015
+ O-lignoceroylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a lignoceroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a linoleoyl group.
+ MOP:0003149
+ has_participant: CHEBI:32386
+ O-linoleoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a linoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a parinaroyl group.
+ MOP:0003150
+ has_participant: CHEBI:50501
+ O-parinaroylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cis-parinaroyl group.
+ MOP:0003151
+ has_participant: CHEBI:32415
+ O-cis-parinaroylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cis-parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trans-parinaroyl group.
+ MOP:0003152
+ has_participant: CHEBI:32417
+ O-trans-parinaroylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trans-parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a gamma-glutamyl group.
+ MOP:0003153
+ has_participant: CHEBI:24190
+ O-gamma-glutamylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-gamma-glutamyl group.
+ MOP:0003154
+ has_participant: CHEBI:32474
+ O-L-gamma-glutamylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-gamma-glutamyl group.
+ MOP:0003155
+ has_participant: CHEBI:32480
+ O-D-gamma-glutamylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glucuronosyl group.
+ MOP:0003156
+ has_participant: CHEBI:24303
+ O-glucuronosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glucuronosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-glucuronoyl group.
+ MOP:0003157
+ has_participant: CHEBI:24307
+ O-D-glucuronoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-glucuronoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glyceroyl 2,3-dihydroxypropanoyl group.
+ MOP:0003158
+ has_participant: CHEBI:24363
+ O-glyceroyl 2,3-dihydroxypropanoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glyceroyl 2,3-dihydroxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glyceryl group.
+ MOP:0003159
+ has_participant: CHEBI:24364
+ O-glycerylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glyceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glycidoyl 2,3-epoxypropanoyl group.
+ MOP:0003160
+ has_participant: CHEBI:24365
+ O-glycidoyl 2,3-epoxypropanoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glycidoyl 2,3-epoxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glycoloyl group.
+ MOP:0003161
+ has_participant: CHEBI:30884
+ O-glycoloylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glycoloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glycosyl group.
+ MOP:0003162
+ has_participant: CHEBI:24403
+ O-glycosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glycosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a galactosyl group.
+ MOP:0003163
+ has_participant: CHEBI:24164
+ O-galactosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-D-galactosyl group.
+ MOP:0003168
+ MOP:0003164
+ has_participant: CHEBI:22778
+ O-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-L-fucosyl-1,2-beta-D-galactosyl group.
+ MOP:0003165
+ has_participant: CHEBI:16124
+ O-alpha-L-fucosyl-1,2-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-L-fucosyl-1,2-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ MOP:0003166
+ has_participant: CHEBI:16361
+ O-alpha-N-acetylneuraminyl-2,3-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ MOP:0003167
+ has_participant: CHEBI:17483
+ O-alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glucosyl group.
+ MOP:0003172
+ MOP:0003169
+ has_participant: CHEBI:24281
+ O-glucosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosyl group.
+ MOP:0003170
+ has_participant: CHEBI:17227
+ O-D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-galactosyl-1,4beta-D-glucosyl group.
+ MOP:0003171
+ has_participant: CHEBI:20966
+ O-D-galactosyl-1,4beta-D-glucosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-galactosyl-1,4beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-glucosyl group.
+ MOP:0003173
+ has_participant: CHEBI:30684
+ O-alpha-glucosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-glucosyl group.
+ MOP:0003174
+ has_participant: CHEBI:30697
+ O-beta-glucosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-galactosyl-(1->4)-beta-D-glucosyl group.
+ MOP:0003175
+ has_participant: CHEBI:18018
+ O-D-galactosyl-(1->4)-beta-D-glucosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-galactosyl-(1->4)-beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glycosaminyl group.
+ MOP:0003176
+ has_participant: CHEBI:24399
+ O-glycosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glycosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a galactosaminyl group.
+ MOP:0003177
+ has_participant: CHEBI:24160
+ O-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-D-galactosaminyl group.
+ MOP:0003178
+ has_participant: CHEBI:21507
+ O-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0003179
+ has_participant: CHEBI:17850
+ O-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ MOP:0003180
+ has_participant: CHEBI:16565
+ O-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ MOP:0003181
+ has_participant: CHEBI:16901
+ O-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0003182
+ has_participant: CHEBI:15876
+ O-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0003183
+ has_participant: CHEBI:17723
+ O-beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ MOP:0003184
+ has_participant: CHEBI:16117
+ O-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ MOP:0003185
+ has_participant: CHEBI:22783
+ O-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0003186
+ has_participant: CHEBI:17581
+ O-N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminyl group.
+ MOP:0003187
+ has_participant: CHEBI:16250
+ O-N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminyl group.
+ MOP:0003188
+ has_participant: CHEBI:16478
+ O-N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glucosaminyl group.
+ MOP:0003189
+ has_participant: CHEBI:24272
+ O-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-D-glucosaminyl group.
+ MOP:0003190
+ has_participant: CHEBI:21524
+ O-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ MOP:0003191
+ has_participant: CHEBI:18914
+ O-1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 3-O-beta-D-galactosyl-N-acetyl-D-glucosaminyl group.
+ MOP:0003192
+ has_participant: CHEBI:18915
+ O-3-O-beta-D-galactosyl-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 3-O-beta-D-galactosyl-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ MOP:0003193
+ has_participant: CHEBI:18939
+ O-1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0003194
+ has_participant: CHEBI:17571
+ O-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0003195
+ has_participant: CHEBI:17785
+ O-alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0003196
+ has_participant: CHEBI:22381
+ O-alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminyl group.
+ MOP:0003197
+ has_participant: CHEBI:22779
+ O-beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0003198
+ has_participant: CHEBI:21580
+ O-N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0003199
+ has_participant: CHEBI:21581
+ O-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0003200
+ has_participant: CHEBI:21582
+ O-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0003201
+ has_participant: CHEBI:21583
+ O-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0003202
+ has_participant: CHEBI:16059
+ O-N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0003203
+ has_participant: CHEBI:16198
+ O-N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an iduronosyl group.
+ MOP:0003204
+ has_participant: CHEBI:24770
+ O-iduronosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an iduronosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-inosinyl group.
+ MOP:0003205
+ has_participant: CHEBI:24845
+ O-5'-inosinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-inosinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a mannosyl group.
+ MOP:0003209
+ MOP:0003206
+ has_participant: CHEBI:25171
+ O-mannosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a (N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ MOP:0003207
+ has_participant: CHEBI:18638
+ O-(N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a (N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-D-mannosyl-1,3-(r1)-beta-D-mannosyl group.
+ MOP:0003208
+ has_participant: CHEBI:22406
+ O-alpha-D-mannosyl-1,3-(r1)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-D-mannosyl-1,3-(r1)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-mannosyl group.
+ MOP:0003210
+ has_participant: CHEBI:30689
+ O-alpha-mannosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosyl group.
+ MOP:0003211
+ has_participant: CHEBI:32618
+ O-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosyl group.
+ MOP:0003212
+ has_participant: CHEBI:32890
+ O-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ MOP:0003213
+ has_participant: CHEBI:21589
+ O-N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosyl group.
+ MOP:0003214
+ has_participant: CHEBI:32601
+ O-N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosyl group.
+ MOP:0003215
+ has_participant: CHEBI:32602
+ O-N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-D-mannosyl-(1->3)-beta-D-mannosyl group.
+ MOP:0003216
+ has_participant: CHEBI:32591
+ O-alpha-D-mannosyl-(1->3)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-D-mannosyl-(1->3)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a neuraminosyl group.
+ MOP:0003217
+ has_participant: CHEBI:25509
+ O-neuraminosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a neuraminosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a neuraminoyl group.
+ MOP:0003218
+ has_participant: CHEBI:25510
+ O-neuraminoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a neuraminoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a ribosyl group.
+ MOP:0003221
+ MOP:0003219
+ has_participant: CHEBI:26566
+ O-ribosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a ribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an adenosinediphosphoribosyl group.
+ MOP:0003220
+ has_participant: CHEBI:22259
+ O-adenosinediphosphoribosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an adenosinediphosphoribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-deoxyribosyl group.
+ MOP:0003222
+ has_participant: CHEBI:30720
+ O-2-deoxyribosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-deoxyribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sialosyl group.
+ MOP:0003223
+ has_participant: CHEBI:26668
+ O-sialosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sialosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a hemicystyl group.
+ MOP:0003224
+ has_participant: CHEBI:24492
+ O-hemicystylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a hemicystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a mevalonoyl group.
+ MOP:0003225
+ has_participant: CHEBI:25353
+ O-mevalonoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a mevalonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a montanoyl group.
+ MOP:0003226
+ has_participant: CHEBI:25417
+ O-montanoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a montanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a muramyl group.
+ MOP:0003227
+ has_participant: CHEBI:25433
+ O-muramylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nucleotidyl group.
+ MOP:0003228
+ has_participant: CHEBI:25613
+ O-nucleotidylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nucleotidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-adenylyl group.
+ MOP:0003229
+ has_participant: CHEBI:22263
+ O-5'-adenylylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-adenylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-cytidylyl group.
+ MOP:0003230
+ has_participant: CHEBI:23526
+ O-5'-cytidylylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-cytidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-thymidylyl group.
+ MOP:0003231
+ has_participant: CHEBI:27003
+ O-5'-thymidylylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-thymidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-uridylyl group.
+ MOP:0003232
+ has_participant: CHEBI:27244
+ O-5'-uridylylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-uridylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-guanylyl group.
+ MOP:0003233
+ has_participant: CHEBI:24460
+ O-5'-guanylylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-guanylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-ribothymidylyl group.
+ MOP:0003234
+ has_participant: CHEBI:26569
+ O-5'-ribothymidylylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-ribothymidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-inosinylyl group.
+ MOP:0003235
+ has_participant: CHEBI:33512
+ O-5'-inosinylylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-inosinylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pantothenyl group.
+ MOP:0003236
+ has_participant: CHEBI:25850
+ O-pantothenylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pantothenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pantoyl group.
+ MOP:0003237
+ has_participant: CHEBI:25851
+ O-pantoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pantoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a peptidyl group.
+ MOP:0003238
+ has_participant: CHEBI:25907
+ O-peptidylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a peptidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phthalyl group.
+ MOP:0003239
+ has_participant: CHEBI:26096
+ O-phthalylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phthalyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a propionyl group.
+ MOP:0003240
+ has_participant: CHEBI:26294
+ O-propionylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a propionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pyruvoyl group.
+ MOP:0003241
+ has_participant: CHEBI:45360
+ O-pyruvoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pyruvoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a retinoyl group.
+ MOP:0003242
+ has_participant: CHEBI:26539
+ O-retinoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a retinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sialoyl group.
+ MOP:0003243
+ has_participant: CHEBI:26670
+ O-sialoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 3-carboxypropanoyl group.
+ MOP:0003244
+ has_participant: CHEBI:26810
+ O-3-carboxypropanoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 3-carboxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trienoyl group.
+ MOP:0003245
+ has_participant: CHEBI:27107
+ O-trienoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an anilinocarbonyl group.
+ MOP:0003246
+ has_participant: CHEBI:30692
+ O-anilinocarbonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an anilinocarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pteroyl group.
+ MOP:0003247
+ has_participant: CHEBI:26379
+ O-pteroylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pteroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 3-carboxyprop-2-enoyl group.
+ MOP:0003248
+ has_participant: CHEBI:37953
+ O-3-carboxyprop-2-enoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a (Z)-3-carboxyprop-2-enoyl group.
+ MOP:0003249
+ has_participant: CHEBI:25122
+ O-(Z)-3-carboxyprop-2-enoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a (Z)-3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a (E)-3-carboxyprop-2-enoyl group.
+ MOP:0003250
+ has_participant: CHEBI:24126
+ O-(E)-3-carboxyprop-2-enoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a (E)-3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2,6-dichlorobenzoyl group.
+ MOP:0003251
+ has_participant: CHEBI:48625
+ O-2,6-dichlorobenzoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2,6-dichlorobenzoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-muramyl group.
+ MOP:0003252
+ has_participant: CHEBI:30701
+ O-alpha-muramylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-muramyl group.
+ MOP:0003253
+ has_participant: CHEBI:30702
+ O-beta-muramylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a beta-muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a dihydrolipoyl group.
+ MOP:0003254
+ has_participant: CHEBI:50488
+ O-dihydrolipoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sinapoyl group.
+ MOP:0003255
+ has_participant: CHEBI:50561
+ O-sinapoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sinapoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carboxyacetyl group.
+ MOP:0003256
+ has_participant: CHEBI:50650
+ O-carboxyacetylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carboxyacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a divalent carboacyl group.
+ MOP:0003257
+ has_participant: CHEBI:23855
+ O-divalent carboacylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a divalent carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an aspartoyl group.
+ MOP:0003258
+ has_participant: CHEBI:22663
+ O-aspartoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-aspartoyl group.
+ MOP:0003259
+ has_participant: CHEBI:32464
+ O-L-aspartoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-aspartoyl group.
+ MOP:0003260
+ has_participant: CHEBI:32468
+ O-D-aspartoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a citraconoyl group.
+ MOP:0003261
+ has_participant: CHEBI:23315
+ O-citraconoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a citraconoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glutamoyl group.
+ MOP:0003262
+ has_participant: CHEBI:24322
+ O-glutamoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-glutamoyl group.
+ MOP:0003263
+ has_participant: CHEBI:32481
+ O-D-glutamoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-glutamoyl group.
+ MOP:0003264
+ has_participant: CHEBI:32475
+ O-L-glutamoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a maloyl group.
+ MOP:0003265
+ has_participant: CHEBI:25138
+ O-maloylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a maloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phthaloyl group.
+ MOP:0003266
+ has_participant: CHEBI:26095
+ O-phthaloylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phthaloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a succinyl group.
+ MOP:0003267
+ has_participant: CHEBI:37952
+ O-succinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a succinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a butenedioyl group.
+ MOP:0003268
+ has_participant: CHEBI:37954
+ O-butenedioylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a butenedioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a fumaroyl group.
+ MOP:0003269
+ has_participant: CHEBI:24125
+ O-fumaroylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a fumaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a maleoyl group.
+ MOP:0003270
+ has_participant: CHEBI:25121
+ O-maleoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a maleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a hexanedioyl group.
+ MOP:0003271
+ has_participant: CHEBI:48082
+ O-hexanedioylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a hexanedioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a malonyl group.
+ MOP:0003272
+ has_participant: CHEBI:25134
+ O-malonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a malonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an ornithyl group.
+ MOP:0003273
+ has_participant: CHEBI:46929
+ O-ornithylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an ornithyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-ornithyl group.
+ MOP:0003274
+ has_participant: CHEBI:44700
+ O-L-ornithylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-ornithyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a half-cystyl group.
+ MOP:0003275
+ has_participant: CHEBI:30770
+ O-half-cystylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a half-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-tyrosin-O(4)-yl group.
+ MOP:0003276
+ has_participant: CHEBI:32768
+ O-L-tyrosin-O(4)-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-threonin-O(3)-yl group.
+ MOP:0003277
+ has_participant: CHEBI:32825
+ O-L-threonin-O(3)-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an L-threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-tyrosin-O(4)-yl group.
+ MOP:0003278
+ has_participant: CHEBI:32780
+ O-D-tyrosin-O(4)-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-threonin-O(3)-yl group.
+ MOP:0003279
+ has_participant: CHEBI:32831
+ O-D-threonin-O(3)-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a D-threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tyrosin-O(4)-yl group.
+ MOP:0003280
+ has_participant: CHEBI:32788
+ O-tyrosin-O(4)-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a threonin-O(3)-yl group.
+ MOP:0003281
+ has_participant: CHEBI:26985
+ O-threonin-O(3)-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an oxalyl group.
+ MOP:0003282
+ has_participant: CHEBI:30870
+ O-oxalylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an oxalyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a fumagillin-2-yl group.
+ MOP:0003283
+ has_participant: CHEBI:42601
+ O-fumagillin-2-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a fumagillin-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acetoacetyl group.
+ MOP:0003284
+ has_participant: CHEBI:48051
+ O-acetoacetylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acetoacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-linolenoyl group.
+ MOP:0003285
+ has_participant: CHEBI:32388
+ O-alpha-linolenoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alpha-linolenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a gamma-linolenoyl group.
+ MOP:0003286
+ has_participant: CHEBI:32390
+ O-gamma-linolenoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a gamma-linolenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carbamimidoyl group.
+ MOP:0003287
+ has_participant: CHEBI:48090
+ O-carbamimidoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carbamimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a formimidoyl group.
+ MOP:0003288
+ has_participant: CHEBI:24084
+ O-formimidoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a formimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trifluoroacetyl group.
+ MOP:0003289
+ has_participant: CHEBI:45888
+ O-trifluoroacetylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trifluoroacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carboxymethyl group.
+ MOP:0003290
+ has_participant: CHEBI:41402
+ O-carboxymethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carboxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a methylenecarbonyl group.
+ MOP:0003291
+ has_participant: CHEBI:43923
+ O-methylenecarbonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a methylenecarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-hydroxyacetimidoyl group.
+ MOP:0003292
+ has_participant: CHEBI:48055
+ O-N-hydroxyacetimidoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-hydroxyacetimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acryloyl group.
+ MOP:0003293
+ has_participant: CHEBI:48077
+ O-acryloylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acryloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tert-butoxycarbonyl group.
+ MOP:0003294
+ has_participant: CHEBI:48502
+ O-tert-butoxycarbonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tert-butoxycarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfanediyl group.
+ MOP:0003295
+ has_participant: CHEBI:29830
+ O-sulfanediylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phenylsulfanyl group.
+ MOP:0003296
+ has_participant: CHEBI:48499
+ O-phenylsulfanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phenylsulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a methylsulfanyl group.
+ MOP:0003297
+ has_participant: CHEBI:48563
+ O-methylsulfanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a methylsulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfaniumyl group.
+ MOP:0003298
+ has_participant: CHEBI:36945
+ O-sulfaniumylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a disulfanidyl group.
+ MOP:0003299
+ has_participant: CHEBI:29838
+ O-disulfanidylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a disulfanidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a disulfanediyl group.
+ MOP:0003300
+ has_participant: CHEBI:29826
+ O-disulfanediylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a disulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a disulfanyl group.
+ MOP:0003301
+ has_participant: CHEBI:30605
+ O-disulfanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a disulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tetrasulfanyl group.
+ MOP:0003302
+ has_participant: CHEBI:30607
+ O-tetrasulfanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tetrasulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tetrasulfanediyl group.
+ MOP:0003303
+ has_participant: CHEBI:29836
+ O-tetrasulfanediylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tetrasulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trisulfanyl group.
+ MOP:0003304
+ has_participant: CHEBI:30606
+ O-trisulfanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trisulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trisulfanediyl group.
+ MOP:0003305
+ has_participant: CHEBI:29834
+ O-trisulfanediylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trisulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pentasulfanyl group.
+ MOP:0003306
+ has_participant: CHEBI:30608
+ O-pentasulfanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pentasulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a diselanyl group.
+ MOP:0003307
+ has_participant: CHEBI:30602
+ O-diselanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a diselanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tellanyl group.
+ MOP:0003308
+ has_participant: CHEBI:30458
+ O-tellanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tellanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tellanediyl group.
+ MOP:0003309
+ has_participant: CHEBI:30455
+ O-tellanediylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tellanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tellaniumyl group.
+ MOP:0003310
+ has_participant: CHEBI:30447
+ O-tellaniumylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tellaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a ditellanyl group.
+ MOP:0003311
+ has_participant: CHEBI:30601
+ O-ditellanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a ditellanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an amidyl group.
+ MOP:0003312
+ has_participant: CHEBI:48373
+ O-amidylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an amidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an azanediyl group.
+ MOP:0003313
+ has_participant: CHEBI:29343
+ O-azanediylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an azanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-aminoethyl group.
+ MOP:0003314
+ has_participant: CHEBI:22502
+ O-2-aminoethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-aminoethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 4-aminobutyl group.
+ MOP:0003315
+ has_participant: CHEBI:50339
+ O-4-aminobutylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 4-aminobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an azanetriyl group.
+ MOP:0003316
+ has_participant: CHEBI:30228
+ O-azanetriylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an azanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a hydrazine-1,2-diyl group.
+ MOP:0003317
+ has_participant: CHEBI:30098
+ O-hydrazine-1,2-diylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a hydrazine-1,2-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a diazyn-1-ium-1-yl group.
+ MOP:0003318
+ has_participant: CHEBI:30108
+ O-diazyn-1-ium-1-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a diazyn-1-ium-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phosphanetriyl group.
+ MOP:0003319
+ has_participant: CHEBI:30206
+ O-phosphanetriylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phosphanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phosphanediyl group.
+ MOP:0003320
+ has_participant: CHEBI:29944
+ O-phosphanediylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phosphanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phosphanyl group.
+ MOP:0003321
+ has_participant: CHEBI:29936
+ O-phosphanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phosphanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a lambda(5)-phosphanyl group.
+ MOP:0003322
+ has_participant: CHEBI:30284
+ O-lambda(5)-phosphanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a lambda(5)-phosphanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phosphaniumyl group.
+ MOP:0003323
+ has_participant: CHEBI:30279
+ O-phosphaniumylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phosphaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arsanyl group.
+ MOP:0003324
+ has_participant: CHEBI:29759
+ O-arsanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arsanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arsanediyl group.
+ MOP:0003325
+ has_participant: CHEBI:29763
+ O-arsanediylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arsanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arsanetriyl group.
+ MOP:0003326
+ has_participant: CHEBI:29766
+ O-arsanetriylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arsanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arsaniumyl group.
+ MOP:0003327
+ has_participant: CHEBI:29842
+ O-arsaniumylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arsaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a lambda(5)-arsanyl group.
+ MOP:0003328
+ has_participant: CHEBI:30273
+ O-lambda(5)-arsanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a lambda(5)-arsanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a stibaniumyl group.
+ MOP:0003329
+ has_participant: CHEBI:30291
+ O-stibaniumylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a stibaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a lambda(5)-stibanyl group.
+ MOP:0003330
+ has_participant: CHEBI:30293
+ O-lambda(5)-stibanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a lambda(5)-stibanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a boranyl group.
+ MOP:0003331
+ has_participant: CHEBI:33604
+ O-boranylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a boranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a boranetriyl group.
+ MOP:0003332
+ has_participant: CHEBI:30169
+ O-boranetriylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a boranetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a boranediyl group.
+ MOP:0003333
+ has_participant: CHEBI:38988
+ O-boranediylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a boranediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a boranuidyl group.
+ MOP:0003334
+ has_participant: CHEBI:30159
+ O-boranuidylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a boranuidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a germyl group.
+ MOP:0003335
+ has_participant: CHEBI:30542
+ O-germylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a germyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a germanediyl group.
+ MOP:0003336
+ has_participant: CHEBI:30554
+ O-germanediylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a germanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a germanetetrayl group.
+ MOP:0003337
+ has_participant: CHEBI:30547
+ O-germanetetraylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a germanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a germanetriyl group.
+ MOP:0003338
+ has_participant: CHEBI:30544
+ O-germanetriylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a germanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a silyl group.
+ MOP:0003339
+ has_participant: CHEBI:30541
+ O-silylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a silyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a silanediyl group.
+ MOP:0003340
+ has_participant: CHEBI:30587
+ O-silanediylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a silanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a silanetriyl group.
+ MOP:0003341
+ has_participant: CHEBI:30576
+ O-silanetriylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a silanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a silanetetrayl group.
+ MOP:0003342
+ has_participant: CHEBI:30583
+ O-silanetetraylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a silanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a disilanyl group.
+ MOP:0003343
+ has_participant: CHEBI:30594
+ O-disilanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a disilanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alumanyl group.
+ MOP:0003344
+ has_participant: CHEBI:30135
+ O-alumanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alumanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a stannyl group.
+ MOP:0003345
+ has_participant: CHEBI:30540
+ O-stannylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a stannyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a stannanetriyl group.
+ MOP:0003346
+ has_participant: CHEBI:30575
+ O-stannanetriylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a stannanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a plumbanetriyl group.
+ MOP:0003347
+ has_participant: CHEBI:30577
+ O-plumbanetriylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a plumbanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a plumbyl group.
+ MOP:0003348
+ has_participant: CHEBI:30543
+ O-plumbylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a plumbyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a gallanyl group.
+ MOP:0003349
+ has_participant: CHEBI:37119
+ O-gallanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a gallanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an indiganyl group.
+ MOP:0003350
+ has_participant: CHEBI:30431
+ O-indiganylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an indiganyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a thallanyl group.
+ MOP:0003351
+ has_participant: CHEBI:30442
+ O-thallanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a thallanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phosphatidyl group.
+ MOP:0003352
+ has_participant: CHEBI:26025
+ O-phosphatidylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phosphatidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nucleosidyl group.
+ MOP:0003353
+ has_participant: CHEBI:33494
+ O-nucleosidylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nucleosidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a guanosyl group.
+ MOP:0003354
+ has_participant: CHEBI:24459
+ O-guanosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a guanosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an inosyl group.
+ MOP:0003355
+ has_participant: CHEBI:24849
+ O-inosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an inosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a thymidyl group.
+ MOP:0003356
+ has_participant: CHEBI:27002
+ O-thymidylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a thymidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an adenosyl group.
+ MOP:0003357
+ has_participant: CHEBI:33505
+ O-adenosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an adenosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-adenosyl group.
+ MOP:0003358
+ has_participant: CHEBI:22261
+ O-5'-adenosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 5'-adenosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an uridyl group.
+ MOP:0003359
+ has_participant: CHEBI:27243
+ O-uridylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an uridyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cytidyl group.
+ MOP:0003360
+ has_participant: CHEBI:23525
+ O-cytidylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cytidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a dolichyl group.
+ MOP:0003361
+ has_participant: CHEBI:23883
+ O-dolichylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a dolichyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-trans,6-trans-farnesyl group.
+ MOP:0003362
+ has_participant: CHEBI:36535
+ O-2-trans,6-trans-farnesylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-trans,6-trans-farnesyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a margaryl group.
+ MOP:0003363
+ has_participant: CHEBI:32925
+ O-margarylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a margaryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a methyl group.
+ MOP:0003364
+ has_participant: CHEBI:32875
+ O-methylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a methyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a methanetetrayl group.
+ MOP:0003365
+ has_participant: CHEBI:30039
+ O-methanetetraylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a methanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a methanetriyl group.
+ MOP:0003366
+ has_participant: CHEBI:29433
+ O-methanetriylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a methanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trichloromethyl group.
+ MOP:0003367
+ has_participant: CHEBI:30736
+ O-trichloromethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trichloromethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trifluoromethyl group.
+ MOP:0003368
+ has_participant: CHEBI:50127
+ O-trifluoromethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trifluoromethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alkyl group.
+ MOP:0003369
+ has_participant: CHEBI:22323
+ O-alkylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a butyl group.
+ MOP:0003370
+ has_participant: CHEBI:41264
+ O-butylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a ceryl group.
+ MOP:0003371
+ has_participant: CHEBI:23081
+ O-cerylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a ceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a decyl group.
+ MOP:0003372
+ has_participant: CHEBI:23580
+ O-decylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a decyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a dodecyl group.
+ MOP:0003373
+ has_participant: CHEBI:23870
+ O-dodecylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a dodecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a heptyl group.
+ MOP:0003374
+ has_participant: CHEBI:24526
+ O-heptylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a heptyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a hexyl group.
+ MOP:0003375
+ has_participant: CHEBI:24593
+ O-hexylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a hexyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a myricyl group.
+ MOP:0003376
+ has_participant: CHEBI:25453
+ O-myricylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a myricyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a myristyl group.
+ MOP:0003377
+ has_participant: CHEBI:25457
+ O-myristylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a myristyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nonyl group.
+ MOP:0003378
+ has_participant: CHEBI:25589
+ O-nonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an octyl group.
+ MOP:0003379
+ has_participant: CHEBI:25657
+ O-octylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an octyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a palmityl group.
+ MOP:0003380
+ has_participant: CHEBI:25842
+ O-palmitylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a palmityl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pentyl group.
+ MOP:0003381
+ has_participant: CHEBI:25902
+ O-pentylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a propyl group.
+ MOP:0003382
+ has_participant: CHEBI:26308
+ O-propylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a propyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a stearyl group.
+ MOP:0003383
+ has_participant: CHEBI:26755
+ O-stearylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a stearyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an isopropyl group.
+ MOP:0003384
+ has_participant: CHEBI:30353
+ O-isopropylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an isopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an ethyl group.
+ MOP:0003385
+ has_participant: CHEBI:37807
+ O-ethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an ethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an isobutyl group.
+ MOP:0003386
+ has_participant: CHEBI:30356
+ O-isobutylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an isobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pentan-2-yl group.
+ MOP:0003387
+ has_participant: CHEBI:32880
+ O-pentan-2-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pentan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an isopentyl group.
+ MOP:0003388
+ has_participant: CHEBI:30359
+ O-isopentylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an isopentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 3-methylbutan-2-yl group.
+ MOP:0003389
+ has_participant: CHEBI:32882
+ O-3-methylbutan-2-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 3-methylbutan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tert-pentyl group.
+ MOP:0003390
+ has_participant: CHEBI:30360
+ O-tert-pentylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tert-pentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a neopentyl group.
+ MOP:0003391
+ has_participant: CHEBI:30357
+ O-neopentylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a neopentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an undecyl group.
+ MOP:0003392
+ has_participant: CHEBI:32900
+ O-undecylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an undecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tridecyl group.
+ MOP:0003393
+ has_participant: CHEBI:32908
+ O-tridecylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tridecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pentadecyl group.
+ MOP:0003394
+ has_participant: CHEBI:32909
+ O-pentadecylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pentadecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nonadecyl group.
+ MOP:0003395
+ has_participant: CHEBI:32928
+ O-nonadecylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nonadecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arachidyl group.
+ MOP:0003396
+ has_participant: CHEBI:32930
+ O-arachidylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arachidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a henicosyl group.
+ MOP:0003397
+ has_participant: CHEBI:32932
+ O-henicosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a henicosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a behenyl group.
+ MOP:0003398
+ has_participant: CHEBI:32933
+ O-behenylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a behenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tricosyl group.
+ MOP:0003399
+ has_participant: CHEBI:32935
+ O-tricosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tricosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a lignoceryl group.
+ MOP:0003400
+ has_participant: CHEBI:32937
+ O-lignocerylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a lignoceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pentacosyl group.
+ MOP:0003401
+ has_participant: CHEBI:32939
+ O-pentacosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pentacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a heptacosyl group.
+ MOP:0003402
+ has_participant: CHEBI:32942
+ O-heptacosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a heptacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a montanyl group.
+ MOP:0003403
+ has_participant: CHEBI:32944
+ O-montanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a montanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nonacosyl group.
+ MOP:0003404
+ has_participant: CHEBI:32945
+ O-nonacosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nonacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sec-butyl group.
+ MOP:0003405
+ has_participant: CHEBI:45557
+ O-sec-butylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sec-butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tert-butyl group.
+ MOP:0003406
+ has_participant: CHEBI:30355
+ O-tert-butylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tert-butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pentan-3-yl group.
+ MOP:0003407
+ has_participant: CHEBI:32881
+ O-pentan-3-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a pentan-3-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-chloroethyl group.
+ MOP:0003408
+ has_participant: CHEBI:47553
+ O-2-chloroethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-chloroethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 1-chloroethyl group.
+ MOP:0003409
+ has_participant: CHEBI:48099
+ O-1-chloroethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 1-chloroethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a hydrocarbyl group.
+ MOP:0003410
+ has_participant: CHEBI:33248
+ O-hydrocarbylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a hydrocarbyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an aryl group.
+ MOP:0003411
+ has_participant: CHEBI:33338
+ O-arylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an aryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phenyl group.
+ MOP:0003412
+ has_participant: CHEBI:30396
+ O-phenylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a biphenyl-4-yl group.
+ MOP:0003413
+ has_participant: CHEBI:35447
+ O-biphenyl-4-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a biphenyl-4-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a naphthyl group.
+ MOP:0003414
+ has_participant: CHEBI:51140
+ O-naphthylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 1-naphthyl group.
+ MOP:0003415
+ has_participant: CHEBI:51138
+ O-1-naphthylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 1-naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-naphthyl group.
+ MOP:0003416
+ has_participant: CHEBI:51139
+ O-2-naphthylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cycloalkyl group.
+ MOP:0003417
+ has_participant: CHEBI:33441
+ O-cycloalkylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cycloalkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cyclobutyl group.
+ MOP:0003418
+ has_participant: CHEBI:30376
+ O-cyclobutylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cyclobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cyclopropyl group.
+ MOP:0003419
+ has_participant: CHEBI:30364
+ O-cyclopropylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cyclopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alkenyl group.
+ MOP:0003420
+ has_participant: CHEBI:37614
+ O-alkenylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alkenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an oleyl group.
+ MOP:0003421
+ has_participant: CHEBI:25670
+ O-oleylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an oleyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an allyl group.
+ MOP:0003422
+ has_participant: CHEBI:30361
+ O-allylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an allyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an isopropenyl group.
+ MOP:0003423
+ has_participant: CHEBI:30354
+ O-isopropenylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an isopropenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a vinyl group.
+ MOP:0003424
+ has_participant: CHEBI:37603
+ O-vinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a vinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a prenyl group.
+ MOP:0003427
+ MOP:0003425
+ has_participant: CHEBI:26248
+ O-prenylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a prenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phytyl group.
+ MOP:0003426
+ has_participant: CHEBI:26126
+ O-phytylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phytyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a polyprenyl group.
+ MOP:0003428
+ has_participant: CHEBI:26201
+ O-polyprenylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a polyprenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a farnesyl group.
+ MOP:0003429
+ has_participant: CHEBI:24017
+ O-farnesylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a farnesyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a geranyl group.
+ MOP:0003430
+ has_participant: CHEBI:24224
+ O-geranylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a geranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a geranylgeranyl group.
+ MOP:0003431
+ has_participant: CHEBI:24231
+ O-geranylgeranylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a geranylgeranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a retinyl group.
+ MOP:0003432
+ has_participant: CHEBI:26541
+ O-retinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a retinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an adamantan-2-yl group.
+ MOP:0003433
+ has_participant: CHEBI:48078
+ O-adamantan-2-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an adamantan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cycloalkenyl group.
+ MOP:0003434
+ has_participant: CHEBI:48886
+ O-cycloalkenylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cycloalkenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a campholenic cyclohexenyl group.
+ MOP:0003435
+ has_participant: CHEBI:48885
+ O-campholenic cyclohexenylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a campholenic cyclohexenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cyclopentadienyl group.
+ MOP:0003436
+ has_participant: CHEBI:30663
+ O-cyclopentadienylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an eta(5)-cyclopentadienyl group.
+ MOP:0003437
+ has_participant: CHEBI:36763
+ O-eta(5)-cyclopentadienylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an eta(5)-cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an eta(1)-cyclopentadienyl group.
+ MOP:0003438
+ has_participant: CHEBI:36764
+ O-eta(1)-cyclopentadienylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an eta(1)-cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an ethene-1,2-diyl group.
+ MOP:0003439
+ has_participant: CHEBI:46880
+ O-ethene-1,2-diylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an ethene-1,2-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arachidonyl group.
+ MOP:0003440
+ has_participant: CHEBI:22612
+ O-arachidonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arachidonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a benzyl group.
+ MOP:0003441
+ has_participant: CHEBI:22744
+ O-benzylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a benzyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an anthracen-1-yl group.
+ MOP:0003442
+ has_participant: CHEBI:48287
+ O-anthracen-1-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an anthracen-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an anthracen-2-yl group.
+ MOP:0003443
+ has_participant: CHEBI:48371
+ O-anthracen-2-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an anthracen-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an imidazolyl group.
+ MOP:0003444
+ has_participant: CHEBI:50052
+ O-imidazolylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an imidazolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an imidazol-1-yl group.
+ MOP:0003445
+ has_participant: CHEBI:50053
+ O-imidazol-1-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an imidazol-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an imidazol-2-yl group.
+ MOP:0003446
+ has_participant: CHEBI:50054
+ O-imidazol-2-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an imidazol-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an imidazol-5-yl group.
+ MOP:0003447
+ has_participant: CHEBI:50055
+ O-imidazol-5-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an imidazol-5-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an imidazol-4-yl group.
+ MOP:0003448
+ has_participant: CHEBI:50056
+ O-imidazol-4-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an imidazol-4-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a furyl group.
+ MOP:0003449
+ has_participant: CHEBI:24131
+ O-furylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-furyl group.
+ MOP:0003450
+ has_participant: CHEBI:19586
+ O-2-furylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 3-furyl group.
+ MOP:0003451
+ has_participant: CHEBI:20025
+ O-3-furylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 3-furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a thienyl group.
+ MOP:0003452
+ has_participant: CHEBI:37991
+ O-thienylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-thienyl group.
+ MOP:0003453
+ has_participant: CHEBI:35849
+ O-2-thienylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 3-thienyl group.
+ MOP:0003454
+ has_participant: CHEBI:37992
+ O-3-thienylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 3-thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an adenin-9-yl group.
+ MOP:0003455
+ has_participant: CHEBI:30756
+ O-adenin-9-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an adenin-9-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a guanin-9-yl group.
+ MOP:0003456
+ has_participant: CHEBI:30755
+ O-guanin-9-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a guanin-9-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acetimidoyl group.
+ MOP:0003457
+ has_participant: CHEBI:48050
+ O-acetimidoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acetimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an organyl group.
+ MOP:0003458
+ has_participant: CHEBI:33249
+ O-organylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an organyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an organic heterocyclyl group.
+ MOP:0003459
+ has_participant: CHEBI:33453
+ O-organic heterocyclylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an organic heterocyclyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a heteroaryl group.
+ MOP:0003460
+ has_participant: CHEBI:33470
+ O-heteroarylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a heteroaryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 4,4'-dimethoxytriphenylmethyl group.
+ MOP:0003461
+ has_participant: CHEBI:51095
+ O-4,4'-dimethoxytriphenylmethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 4,4'-dimethoxytriphenylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tauryl group.
+ MOP:0003462
+ has_participant: CHEBI:26861
+ O-taurylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tauryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a triflyl group.
+ MOP:0003463
+ has_participant: CHEBI:48548
+ O-triflylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a triflyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glycidyl group.
+ MOP:0003464
+ has_participant: CHEBI:24366
+ O-glycidylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a glycidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfanylmethyl group.
+ MOP:0003465
+ has_participant: CHEBI:50326
+ O-sulfanylmethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfanylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a selanylmethyl group.
+ MOP:0003466
+ has_participant: CHEBI:50327
+ O-selanylmethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a selanylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-carboxyethyl group.
+ MOP:0003467
+ has_participant: CHEBI:50329
+ O-2-carboxyethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-carboxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-amino-2-oxoethyl group.
+ MOP:0003468
+ has_participant: CHEBI:50330
+ O-2-amino-2-oxoethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-amino-2-oxoethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 3-amino-3-oxopropyl group.
+ MOP:0003469
+ has_participant: CHEBI:50331
+ O-3-amino-3-oxopropylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 3-amino-3-oxopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-(methylsulfanyl)ethyl group.
+ MOP:0003470
+ has_participant: CHEBI:50332
+ O-2-(methylsulfanyl)ethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-(methylsulfanyl)ethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 4-hydroxybenzyl group.
+ MOP:0003471
+ has_participant: CHEBI:50336
+ O-4-hydroxybenzylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 4-hydroxybenzyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 1H-indol-3-ylmethyl group.
+ MOP:0003472
+ has_participant: CHEBI:50337
+ O-1H-indol-3-ylmethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 1H-indol-3-ylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 1H-imidazol-4-ylmethyl group.
+ MOP:0003473
+ has_participant: CHEBI:50338
+ O-1H-imidazol-4-ylmethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 1H-imidazol-4-ylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 3-carbamimidamidopropyl group.
+ MOP:0003474
+ has_participant: CHEBI:50340
+ O-3-carbamimidamidopropylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 3-carbamimidamidopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a hydroxymethyl group.
+ MOP:0003475
+ has_participant: CHEBI:24712
+ O-hydroxymethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a hydroxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 1-hydroxyethyl group.
+ MOP:0003476
+ has_participant: CHEBI:50341
+ O-1-hydroxyethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 1-hydroxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a haloalkyl group.
+ MOP:0003477
+ has_participant: CHEBI:50491
+ O-haloalkylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a haloalkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-(trimethylsilyl)ethoxymethyl group.
+ MOP:0003478
+ has_participant: CHEBI:51093
+ O-2-(trimethylsilyl)ethoxymethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-(trimethylsilyl)ethoxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acyl group.
+ MOP:0003479
+ has_participant: CHEBI:22221
+ O-acylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an organoheteryl group.
+ MOP:0003480
+ has_participant: CHEBI:33456
+ O-organoheterylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an organoheteryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an oxalosulfanyl group.
+ MOP:0003481
+ has_participant: CHEBI:30874
+ O-oxalosulfanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an oxalosulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an organosilyl group.
+ MOP:0003482
+ has_participant: CHEBI:33478
+ O-organosilylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an organosilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trimethylsilyl group.
+ MOP:0003483
+ has_participant: CHEBI:51088
+ O-trimethylsilylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trimethylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a triisopropylsilyl group.
+ MOP:0003484
+ has_participant: CHEBI:51089
+ O-triisopropylsilylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a triisopropylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tert-butyldiphenylsilyl group.
+ MOP:0003485
+ has_participant: CHEBI:51090
+ O-tert-butyldiphenylsilylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tert-butyldiphenylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tert-butyldimethylsilyl group.
+ MOP:0003486
+ has_participant: CHEBI:51091
+ O-tert-butyldimethylsilylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tert-butyldimethylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a thioacyl group.
+ MOP:0003487
+ has_participant: CHEBI:49063
+ O-thioacylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a thioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carbothioacyl group.
+ MOP:0003488
+ has_participant: CHEBI:49066
+ O-carbothioacylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an univalent carbothioacyl group.
+ MOP:0003489
+ has_participant: CHEBI:49067
+ O-univalent carbothioacylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an univalent carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a divalent carbothioacyl group.
+ MOP:0003490
+ has_participant: CHEBI:49068
+ O-divalent carbothioacylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a divalent carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carbonimidoyl group.
+ MOP:0003491
+ has_participant: CHEBI:29815
+ O-carbonimidoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carbonimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a thiocarbonyl group.
+ MOP:0003492
+ has_participant: CHEBI:30256
+ O-thiocarbonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a thiocarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a (fluoren-9-ylmethoxy)carbonyl group.
+ MOP:0003493
+ has_participant: CHEBI:48605
+ O-(fluoren-9-ylmethoxy)carbonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a (fluoren-9-ylmethoxy)carbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carbonyl group.
+ MOP:0003494
+ has_participant: CHEBI:23019
+ O-carbonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a carbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cytosin-1-yl group.
+ MOP:0003495
+ has_participant: CHEBI:30758
+ O-cytosin-1-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a cytosin-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a thymin-1-yl group.
+ MOP:0003496
+ has_participant: CHEBI:30757
+ O-thymin-1-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a thymin-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an uracil-1-yl group.
+ MOP:0003497
+ has_participant: CHEBI:30759
+ O-uracil-1-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an uracil-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a morpholin-4-ylsulfonyl group.
+ MOP:0003498
+ has_participant: CHEBI:45701
+ O-morpholin-4-ylsulfonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a morpholin-4-ylsulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acetohydrazonoyl group.
+ MOP:0003499
+ has_participant: CHEBI:48054
+ O-acetohydrazonoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acetohydrazonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-hydroxyethyl group.
+ MOP:0003500
+ has_participant: CHEBI:44730
+ O-2-hydroxyethylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a 2-hydroxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an aminosulfinyl group.
+ MOP:0003501
+ has_participant: CHEBI:48257
+ O-aminosulfinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an aminosulfinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a disiloxanyl group.
+ MOP:0003502
+ has_participant: CHEBI:48142
+ O-disiloxanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a disiloxanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a disiloxane-1,3-diyl group.
+ MOP:0003503
+ has_participant: CHEBI:48143
+ O-disiloxane-1,3-diylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a disiloxane-1,3-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an azinoyl group.
+ MOP:0003504
+ has_participant: CHEBI:29771
+ O-azinoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an azinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an azonoyl group.
+ MOP:0003505
+ has_participant: CHEBI:37768
+ O-azonoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an azonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phosphorothioyl group.
+ MOP:0003506
+ has_participant: CHEBI:32412
+ O-phosphorothioylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phosphorothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phosphonothioyl group.
+ MOP:0003507
+ has_participant: CHEBI:32413
+ O-phosphonothioylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phosphonothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arsonoyl group.
+ MOP:0003508
+ has_participant: CHEBI:29848
+ O-arsonoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arsonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arsinoyl group.
+ MOP:0003509
+ has_participant: CHEBI:30277
+ O-arsinoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arsinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a stiboryl group.
+ MOP:0003510
+ has_participant: CHEBI:48439
+ O-stiborylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a stiboryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfamoyl group.
+ MOP:0003511
+ has_participant: CHEBI:48266
+ O-sulfamoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a S-aminosulfinimidoyl group.
+ MOP:0003512
+ has_participant: CHEBI:48254
+ O-S-aminosulfinimidoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a S-aminosulfinimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a S-aminosulfonimidoyl group.
+ MOP:0003513
+ has_participant: CHEBI:48264
+ O-S-aminosulfonimidoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a S-aminosulfonimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a chloryl group.
+ MOP:0003514
+ has_participant: CHEBI:29883
+ O-chlorylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a chloryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a chlorosyl group.
+ MOP:0003515
+ has_participant: CHEBI:29878
+ O-chlorosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a chlorosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a perchloryl group.
+ MOP:0003516
+ has_participant: CHEBI:29877
+ O-perchlorylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a perchloryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a bromosyl group.
+ MOP:0003517
+ has_participant: CHEBI:29871
+ O-bromosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a bromosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a bromyl group.
+ MOP:0003518
+ has_participant: CHEBI:29881
+ O-bromylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a bromyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a perbromyl group.
+ MOP:0003519
+ has_participant: CHEBI:29891
+ O-perbromylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a perbromyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an iodosyl group.
+ MOP:0003520
+ has_participant: CHEBI:29897
+ O-iodosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an iodosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an iodyl group.
+ MOP:0003521
+ has_participant: CHEBI:29904
+ O-iodylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an iodyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a periodyl group.
+ MOP:0003522
+ has_participant: CHEBI:29908
+ O-periodylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a periodyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a fluorosyl group.
+ MOP:0003523
+ has_participant: CHEBI:30241
+ O-fluorosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a fluorosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfonyl group.
+ MOP:0003539
+ MOP:0003524
+ has_participant: CHEBI:29825
+ O-sulfonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acetoxysulfonyl group.
+ MOP:0003525
+ has_participant: CHEBI:48065
+ O-acetoxysulfonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acetoxysulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfonothioyl group.
+ MOP:0003526
+ has_participant: CHEBI:29828
+ O-sulfonothioylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfonothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfinothioyl group.
+ MOP:0003527
+ has_participant: CHEBI:29827
+ O-sulfinothioylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfinothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfonodithioyl group.
+ MOP:0003528
+ has_participant: CHEBI:29835
+ O-sulfonodithioylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfonodithioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trioxidanyl group.
+ MOP:0003529
+ has_participant: CHEBI:29791
+ O-trioxidanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trioxidanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trioxidanediyl group.
+ MOP:0003530
+ has_participant: CHEBI:30493
+ O-trioxidanediylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a trioxidanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a heterocyclyl group.
+ MOP:0003531
+ has_participant: CHEBI:48271
+ O-heterocyclylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a heterocyclyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phosphoramidochloridoyl group.
+ MOP:0003532
+ has_participant: CHEBI:48229
+ O-phosphoramidochloridoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a phosphoramidochloridoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a S-aminosulfonodiimidoyl group.
+ MOP:0003533
+ has_participant: CHEBI:48265
+ O-S-aminosulfonodiimidoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a S-aminosulfonodiimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an aminosulfanyl group.
+ MOP:0003534
+ has_participant: CHEBI:48252
+ O-aminosulfanylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an aminosulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfinyl group.
+ MOP:0003535
+ has_participant: CHEBI:29822
+ O-sulfinylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arsoryl group.
+ MOP:0003536
+ has_participant: CHEBI:30274
+ O-arsorylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an arsoryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an azanediidyl group.
+ MOP:0003537
+ has_participant: CHEBI:30227
+ O-azanediidylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an azanediidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfinimidoyl group.
+ MOP:0003538
+ has_participant: CHEBI:29829
+ O-sulfinimidoylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfinimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tosyl group.
+ MOP:0003540
+ has_participant: CHEBI:51094
+ O-tosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a tosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a brosyl group.
+ MOP:0003541
+ has_participant: CHEBI:51101
+ O-brosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a brosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nosyl group.
+ MOP:0003542
+ has_participant: CHEBI:51102
+ O-nosylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an indolyl group.
+ MOP:0003544
+ has_participant: CHEBI:51609
+ O-indolylamination
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an indolyl group.
+ RSC:xp
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an indol-1-yl group.
+ MOP:0003545
+ has_participant: CHEBI:51610
+ O-indol-1-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an indol-1-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an indol-2-yl group.
+ MOP:0003546
+ has_participant: CHEBI:51611
+ O-indol-2-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an indol-2-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an indol-3-yl group.
+ MOP:0003547
+ has_participant: CHEBI:51612
+ O-indol-3-ylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an indol-3-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-oxindolyl group.
+ MOP:0003548
+ has_participant: CHEBI:51613
+ O-N-oxindolylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an N-oxindolyl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alkylamino group.
+ MOP:0003549
+ has_participant: CHEBI:22332
+ O-alkylamination
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an alkylamino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a halo group.
+ MOP:0003550
+ has_participant: CHEBI:47854
+ O-halogenation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a halo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a bromo group.
+ MOP:0003551
+ has_participant: CHEBI:47265
+ O-bromination
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a bromo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a chloro group.
+ MOP:0003552
+ has_participant: CHEBI:47853
+ O-chlorination
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a chloro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a fluoro group.
+ MOP:0003553
+ has_participant: CHEBI:42645
+ O-fluorination
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a fluoro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an iodo group.
+ MOP:0003554
+ has_participant: CHEBI:43448
+ O-iodination
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an iodo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an imino group.
+ MOP:0003555
+ has_participant: CHEBI:29342
+ O-imination
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an imino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nitro group.
+ MOP:0003556
+ has_participant: CHEBI:29785
+ O-nitration
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a nitro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a hydroxyamino group.
+ MOP:0003557
+ has_participant: CHEBI:29769
+ O-hydroxyamination
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a hydroxyamino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a thioxo group.
+ MOP:0003558
+ has_participant: CHEBI:29833
+ O-thioxonation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a thioxo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfo group.
+ MOP:0003559
+ has_participant: CHEBI:29922
+ O-sulfonation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a selenono group.
+ MOP:0003560
+ has_participant: CHEBI:29923
+ O-selenonation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a selenono group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a boryl group (-BR'R').
+ MOP:0004000
+ Submitted to ChEBI
+ S-borylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a boryl group (-BR'R').
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a methanidyl group.
+ MOP:0004001
+ has_participant: CHEBI:29361
+ S-methanidylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a methanidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an azaniumyl group.
+ MOP:0004002
+ has_participant: CHEBI:48284
+ S-azaniumylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an azaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a formyl group.
+ MOP:0004003
+ has_participant: CHEBI:42485
+ S-formylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a formyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acetonyl group.
+ MOP:0004004
+ has_participant: CHEBI:48056
+ S-acetonylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acetonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-cystyl group.
+ MOP:0004005
+ has_participant: CHEBI:50057
+ S-L-cystylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-cystinyl group.
+ MOP:0004006
+ has_participant: CHEBI:50066
+ S-L-cystinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-cystinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-cystyl group.
+ MOP:0004007
+ has_participant: CHEBI:50049
+ S-D-cystylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cystinyl group.
+ MOP:0004008
+ has_participant: CHEBI:50050
+ S-cystinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cystinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cystyl group.
+ MOP:0004009
+ has_participant: CHEBI:23514
+ S-cystylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cysteinyl group.
+ MOP:0004010
+ has_participant: CHEBI:23511
+ S-cysteinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-cysteinyl group.
+ MOP:0004011
+ has_participant: CHEBI:32447
+ S-L-cysteinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-cysteinyl group.
+ MOP:0004012
+ has_participant: CHEBI:32452
+ S-D-cysteinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cystein-S-yl group.
+ MOP:0004013
+ has_participant: CHEBI:32795
+ S-cystein-S-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-cystein-S-yl group.
+ MOP:0004014
+ has_participant: CHEBI:32794
+ S-D-cystein-S-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-cystein-S-yl group.
+ MOP:0004015
+ has_participant: CHEBI:32793
+ S-L-cystein-S-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a methionyl group.
+ MOP:0004016
+ has_participant: CHEBI:37902
+ S-methionylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-methionyl group.
+ MOP:0004017
+ has_participant: CHEBI:49038
+ S-L-methionylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-formyl-L-methionyl group.
+ MOP:0004018
+ has_participant: CHEBI:49298
+ S-N-formyl-L-methionylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-formyl-L-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-methionyl group.
+ MOP:0004019
+ has_participant: CHEBI:32640
+ S-D-methionylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an (R)-lipoyl group.
+ MOP:0004020
+ has_participant: CHEBI:38232
+ S-(R)-lipoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an (R)-lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an (S)-lipoyl group.
+ MOP:0004021
+ has_participant: CHEBI:38233
+ S-(S)-lipoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an (S)-lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a lipoyl group.
+ MOP:0004022
+ has_participant: CHEBI:25064
+ S-lipoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an (R)-dihydrolipoyl group.
+ MOP:0004023
+ has_participant: CHEBI:30319
+ S-(R)-dihydrolipoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an (R)-dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an (S)-dihydrolipoyl group.
+ MOP:0004024
+ has_participant: CHEBI:50489
+ S-(S)-dihydrolipoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an (S)-dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-sialoyl group.
+ MOP:0004025
+ has_participant: CHEBI:32960
+ S-alpha-sialoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-sialoyl group.
+ MOP:0004026
+ has_participant: CHEBI:32961
+ S-beta-sialoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glyceroyl group.
+ MOP:0004027
+ has_participant: CHEBI:30750
+ S-glyceroylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glyceroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carboacyl group.
+ MOP:0004028
+ has_participant: CHEBI:37838
+ S-carboacylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an univalent carboacyl group.
+ MOP:0004029
+ has_participant: CHEBI:27207
+ S-univalent carboacylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an univalent carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acetyl group.
+ MOP:0004030
+ has_participant: CHEBI:40574
+ S-acetylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-aminoacyl group.
+ MOP:0004031
+ has_participant: CHEBI:22487
+ S-alpha-aminoacylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-aminoacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alanyl group.
+ MOP:0004032
+ has_participant: CHEBI:22280
+ S-alanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-alanyl group.
+ MOP:0004033
+ has_participant: CHEBI:32433
+ S-L-alanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-alanyl group.
+ MOP:0004034
+ has_participant: CHEBI:32437
+ S-D-alanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-aspartyl group.
+ MOP:0004035
+ has_participant: CHEBI:22445
+ S-alpha-aspartylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-alpha-aspartyl group.
+ MOP:0004036
+ has_participant: CHEBI:32462
+ S-L-alpha-aspartylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-alpha-aspartyl group.
+ MOP:0004037
+ has_participant: CHEBI:32466
+ S-D-alpha-aspartylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-glutamyl group.
+ MOP:0004038
+ has_participant: CHEBI:22453
+ S-alpha-glutamylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-alpha-glutamyl group.
+ MOP:0004039
+ has_participant: CHEBI:46855
+ S-L-alpha-glutamylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-alpha-glutamyl group.
+ MOP:0004040
+ has_participant: CHEBI:32479
+ S-D-alpha-glutamylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pteroylglutamyl group.
+ MOP:0004041
+ has_participant: CHEBI:26380
+ S-pteroylglutamylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pteroylglutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phenylalanyl group.
+ MOP:0004042
+ has_participant: CHEBI:25987
+ S-phenylalanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-phenylalanyl group.
+ MOP:0004043
+ has_participant: CHEBI:32496
+ S-L-phenylalanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-phenylalanyl group.
+ MOP:0004044
+ has_participant: CHEBI:32500
+ S-D-phenylalanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glycyl group.
+ MOP:0004045
+ has_participant: CHEBI:46740
+ S-glycylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glycyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a histidyl group.
+ MOP:0004046
+ has_participant: CHEBI:37906
+ S-histidylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-histidyl group.
+ MOP:0004047
+ has_participant: CHEBI:32514
+ S-L-histidylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-histidyl group.
+ MOP:0004048
+ has_participant: CHEBI:32522
+ S-D-histidylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an isoleucyl group.
+ MOP:0004049
+ has_participant: CHEBI:37905
+ S-isoleucylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-isoleucyl group.
+ MOP:0004050
+ has_participant: CHEBI:32606
+ S-L-isoleucylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-isoleucyl group.
+ MOP:0004051
+ has_participant: CHEBI:32610
+ S-D-isoleucylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a lysyl group.
+ MOP:0004052
+ has_participant: CHEBI:37903
+ S-lysylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-lysyl group.
+ MOP:0004053
+ has_participant: CHEBI:32553
+ S-L-lysylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a deoxyhypusinyl group.
+ MOP:0004054
+ has_participant: CHEBI:50039
+ S-deoxyhypusinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a deoxyhypusinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-lysyl group.
+ MOP:0004055
+ has_participant: CHEBI:32559
+ S-D-lysylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a leucyl group.
+ MOP:0004056
+ has_participant: CHEBI:37904
+ S-leucylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-leucyl group.
+ MOP:0004057
+ has_participant: CHEBI:32621
+ S-L-leucylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-leucyl group.
+ MOP:0004058
+ has_participant: CHEBI:32625
+ S-D-leucylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an asparaginyl group.
+ MOP:0004059
+ has_participant: CHEBI:22656
+ S-asparaginylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-asparaginyl group.
+ MOP:0004060
+ has_participant: CHEBI:50348
+ S-L-asparaginylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-asparaginyl group.
+ MOP:0004061
+ has_participant: CHEBI:32653
+ S-D-asparaginylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a prolyl group.
+ MOP:0004062
+ has_participant: CHEBI:26274
+ S-prolylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-prolyl group.
+ MOP:0004063
+ has_participant: CHEBI:32865
+ S-L-prolylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-prolyl group.
+ MOP:0004064
+ has_participant: CHEBI:32869
+ S-D-prolylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glutaminyl group.
+ MOP:0004065
+ has_participant: CHEBI:24320
+ S-glutaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-glutaminyl group.
+ MOP:0004066
+ has_participant: CHEBI:32667
+ S-L-glutaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-glutaminyl group.
+ MOP:0004067
+ has_participant: CHEBI:32674
+ S-D-glutaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a seryl group.
+ MOP:0004068
+ has_participant: CHEBI:37901
+ S-serylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-seryl group.
+ MOP:0004069
+ has_participant: CHEBI:32838
+ S-L-serylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-seryl group.
+ MOP:0004070
+ has_participant: CHEBI:32842
+ S-D-serylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a threonyl group.
+ MOP:0004071
+ has_participant: CHEBI:37900
+ S-threonylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-threonyl group.
+ MOP:0004072
+ has_participant: CHEBI:32823
+ S-L-threonylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-threonyl group.
+ MOP:0004073
+ has_participant: CHEBI:32829
+ S-D-threonylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a selenocysteinyl group.
+ MOP:0004074
+ has_participant: CHEBI:32755
+ S-selenocysteinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-selenocysteinyl group.
+ MOP:0004075
+ has_participant: CHEBI:32745
+ S-L-selenocysteinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-selenocysteinyl group.
+ MOP:0004076
+ has_participant: CHEBI:32749
+ S-D-selenocysteinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a valyl group.
+ MOP:0004077
+ has_participant: CHEBI:37897
+ S-valylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-valyl group.
+ MOP:0004078
+ has_participant: CHEBI:32853
+ S-L-valylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-valyl group.
+ MOP:0004079
+ has_participant: CHEBI:32857
+ S-D-valylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tryptophyl group.
+ MOP:0004080
+ has_participant: CHEBI:37899
+ S-tryptophylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-tryptophyl group.
+ MOP:0004081
+ has_participant: CHEBI:32706
+ S-L-tryptophylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-tryptophyl group.
+ MOP:0004082
+ has_participant: CHEBI:32718
+ S-D-tryptophylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tyrosyl group.
+ MOP:0004083
+ has_participant: CHEBI:37898
+ S-tyrosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-tyrosyl group.
+ MOP:0004084
+ has_participant: CHEBI:32764
+ S-L-tyrosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-tyrosyl group.
+ MOP:0004085
+ has_participant: CHEBI:32778
+ S-D-tyrosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arginyl group.
+ MOP:0004086
+ has_participant: CHEBI:22619
+ S-arginylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-arginyl group.
+ MOP:0004087
+ has_participant: CHEBI:32684
+ S-L-arginylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-arginyl group.
+ MOP:0004088
+ has_participant: CHEBI:32691
+ S-D-arginylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a benzoyl group.
+ MOP:0004089
+ has_participant: CHEBI:22733
+ S-benzoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a benzoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-aspartyl group.
+ MOP:0004090
+ has_participant: CHEBI:22832
+ S-beta-aspartylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-beta-aspartyl group.
+ MOP:0004091
+ has_participant: CHEBI:32467
+ S-D-beta-aspartylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-beta-aspartyl group.
+ MOP:0004092
+ has_participant: CHEBI:48098
+ S-L-beta-aspartylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a biotinyl group.
+ MOP:0004093
+ has_participant: CHEBI:22885
+ S-biotinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a biotinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a butyryl group.
+ MOP:0004094
+ has_participant: CHEBI:22972
+ S-butyrylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a butyryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carbamoyl group.
+ MOP:0004095
+ has_participant: CHEBI:23004
+ S-carbamoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carbamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a C-aminocarbonohydrazonoyl group.
+ MOP:0004096
+ has_participant: CHEBI:48223
+ S-C-aminocarbonohydrazonoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a C-aminocarbonohydrazonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-(aminomethylidene)hydrazinyl group.
+ MOP:0004097
+ has_participant: CHEBI:48244
+ S-2-(aminomethylidene)hydrazinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-(aminomethylidene)hydrazinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carbamoylcarbamoyl group.
+ MOP:0004098
+ has_participant: CHEBI:48083
+ S-carbamoylcarbamoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carbamoylcarbamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carbamothioyl group.
+ MOP:0004099
+ has_participant: CHEBI:48225
+ S-carbamothioylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carbamothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acetylazanediyl group.
+ MOP:0004100
+ has_participant: CHEBI:48073
+ S-acetylazanediylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acetylazanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an oxamoyl group.
+ MOP:0004101
+ has_participant: CHEBI:48246
+ S-oxamoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an oxamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cholyl group.
+ MOP:0004102
+ has_participant: CHEBI:23220
+ S-cholylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cholyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an enoyl group.
+ MOP:0004103
+ has_participant: CHEBI:23916
+ S-enoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a fatty-acyl group.
+ MOP:0004104
+ has_participant: CHEBI:24027
+ S-fatty-acylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a fatty-acyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arachidonoyl group.
+ MOP:0004105
+ has_participant: CHEBI:22610
+ S-arachidonoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arachidonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arachidoyl group.
+ MOP:0004106
+ has_participant: CHEBI:22614
+ S-arachidoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arachidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a behenoyl group.
+ MOP:0004107
+ has_participant: CHEBI:22696
+ S-behenoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a behenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cerotoyl group.
+ MOP:0004108
+ has_participant: CHEBI:23080
+ S-cerotoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cerotoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a decanoyl group.
+ MOP:0004109
+ has_participant: CHEBI:23574
+ S-decanoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a decanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a dodecenoyl group.
+ MOP:0004110
+ has_participant: CHEBI:23868
+ S-dodecenoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a dodecenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an eleostearoyl group.
+ MOP:0004111
+ has_participant: CHEBI:23908
+ S-eleostearoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an eleostearoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a mycolyl group.
+ MOP:0004112
+ has_participant: CHEBI:25439
+ S-mycolylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a mycolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nervonoyl group.
+ MOP:0004113
+ has_participant: CHEBI:25503
+ S-nervonoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nervonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an octanoyl group.
+ MOP:0004114
+ has_participant: CHEBI:25650
+ S-octanoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an octanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a palmitoleoyl group.
+ MOP:0004115
+ has_participant: CHEBI:25837
+ S-palmitoleoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a palmitoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a palmitoyl group.
+ MOP:0004116
+ has_participant: CHEBI:45021
+ S-palmitoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a palmitoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a stearoyl group.
+ MOP:0004117
+ has_participant: CHEBI:26753
+ S-stearoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a stearoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an undecanoyl group.
+ MOP:0004118
+ has_participant: CHEBI:27190
+ S-undecanoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an undecanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a valeryl group.
+ MOP:0004119
+ has_participant: CHEBI:27265
+ S-valerylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a valeryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a hexanoyl group.
+ MOP:0004120
+ has_participant: CHEBI:24574
+ S-hexanoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a hexanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a heptanoyl group.
+ MOP:0004121
+ has_participant: CHEBI:32363
+ S-heptanoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a heptanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nonanoyl group.
+ MOP:0004122
+ has_participant: CHEBI:25580
+ S-nonanoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nonanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a lauroyl group.
+ MOP:0004123
+ has_participant: CHEBI:32359
+ S-lauroylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a lauroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a myristoyl group.
+ MOP:0004124
+ has_participant: CHEBI:25456
+ S-myristoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a myristoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a docosenoyl group.
+ MOP:0004125
+ has_participant: CHEBI:50479
+ S-docosenoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a docosenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cetoleoyl group.
+ MOP:0004126
+ has_participant: CHEBI:32430
+ S-cetoleoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cetoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an erucoyl group.
+ MOP:0004127
+ has_participant: CHEBI:32394
+ S-erucoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an erucoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an icosenoyl group.
+ MOP:0004128
+ has_participant: CHEBI:50480
+ S-icosenoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an icosenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a gadelaidoyl group.
+ MOP:0004129
+ has_participant: CHEBI:32424
+ S-gadelaidoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a gadelaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a gadoleoyl group.
+ MOP:0004130
+ has_participant: CHEBI:32421
+ S-gadoleoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a gadoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a gondoyl group.
+ MOP:0004131
+ has_participant: CHEBI:32427
+ S-gondoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a gondoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a heptatrienoyl group.
+ MOP:0004132
+ has_participant: CHEBI:50486
+ S-heptatrienoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a heptatrienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trans,trans-hepta-2,4,6-trienoyl group.
+ MOP:0004133
+ has_participant: CHEBI:30771
+ S-trans,trans-hepta-2,4,6-trienoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trans,trans-hepta-2,4,6-trienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an octadecenoyl group.
+ MOP:0004134
+ has_participant: CHEBI:50499
+ S-octadecenoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an octadecenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an octadec-6-enoyl group.
+ MOP:0004135
+ has_participant: CHEBI:50497
+ S-octadec-6-enoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an octadec-6-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a petroselaidoyl group.
+ MOP:0004136
+ has_participant: CHEBI:32378
+ S-petroselaidoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a petroselaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a petroselinoyl group.
+ MOP:0004137
+ has_participant: CHEBI:32376
+ S-petroselinoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a petroselinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a vaccenoyl group.
+ MOP:0004138
+ has_participant: CHEBI:27261
+ S-vaccenoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cis-vaccenoyl group.
+ MOP:0004139
+ has_participant: CHEBI:23313
+ S-cis-vaccenoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cis-vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trans-vaccenoyl group.
+ MOP:0004140
+ has_participant: CHEBI:27080
+ S-trans-vaccenoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trans-vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an octadec-9-enoyl group.
+ MOP:0004141
+ has_participant: CHEBI:50500
+ S-octadec-9-enoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an octadec-9-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an oleoyl group.
+ MOP:0004142
+ has_participant: CHEBI:25667
+ S-oleoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an oleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an elaidoyl group.
+ MOP:0004143
+ has_participant: CHEBI:23904
+ S-elaidoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an elaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a margaroyl group.
+ MOP:0004144
+ has_participant: CHEBI:32367
+ S-margaroylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a margaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a melissoyl group.
+ MOP:0004145
+ has_participant: CHEBI:31016
+ S-melissoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a melissoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a myristoleoyl group.
+ MOP:0004146
+ has_participant: CHEBI:32371
+ S-myristoleoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a myristoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an obtusiloyl group.
+ MOP:0004147
+ has_participant: CHEBI:33162
+ S-obtusiloylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an obtusiloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a lignoceroyl group.
+ MOP:0004148
+ has_participant: CHEBI:31015
+ S-lignoceroylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a lignoceroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a linoleoyl group.
+ MOP:0004149
+ has_participant: CHEBI:32386
+ S-linoleoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a linoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a parinaroyl group.
+ MOP:0004150
+ has_participant: CHEBI:50501
+ S-parinaroylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cis-parinaroyl group.
+ MOP:0004151
+ has_participant: CHEBI:32415
+ S-cis-parinaroylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cis-parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trans-parinaroyl group.
+ MOP:0004152
+ has_participant: CHEBI:32417
+ S-trans-parinaroylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trans-parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a gamma-glutamyl group.
+ MOP:0004153
+ has_participant: CHEBI:24190
+ S-gamma-glutamylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-gamma-glutamyl group.
+ MOP:0004154
+ has_participant: CHEBI:32474
+ S-L-gamma-glutamylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-gamma-glutamyl group.
+ MOP:0004155
+ has_participant: CHEBI:32480
+ S-D-gamma-glutamylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glucuronosyl group.
+ MOP:0004156
+ has_participant: CHEBI:24303
+ S-glucuronosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glucuronosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-glucuronoyl group.
+ MOP:0004157
+ has_participant: CHEBI:24307
+ S-D-glucuronoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-glucuronoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glyceroyl 2,3-dihydroxypropanoyl group.
+ MOP:0004158
+ has_participant: CHEBI:24363
+ S-glyceroyl 2,3-dihydroxypropanoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glyceroyl 2,3-dihydroxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glyceryl group.
+ MOP:0004159
+ has_participant: CHEBI:24364
+ S-glycerylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glyceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glycidoyl 2,3-epoxypropanoyl group.
+ MOP:0004160
+ has_participant: CHEBI:24365
+ S-glycidoyl 2,3-epoxypropanoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glycidoyl 2,3-epoxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glycoloyl group.
+ MOP:0004161
+ has_participant: CHEBI:30884
+ S-glycoloylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glycoloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glycosyl group.
+ MOP:0004162
+ has_participant: CHEBI:24403
+ S-glycosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glycosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a galactosyl group.
+ MOP:0004163
+ has_participant: CHEBI:24164
+ S-galactosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-D-galactosyl group.
+ MOP:0004168
+ MOP:0004164
+ has_participant: CHEBI:22778
+ S-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-L-fucosyl-1,2-beta-D-galactosyl group.
+ MOP:0004165
+ has_participant: CHEBI:16124
+ S-alpha-L-fucosyl-1,2-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-L-fucosyl-1,2-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ MOP:0004166
+ has_participant: CHEBI:16361
+ S-alpha-N-acetylneuraminyl-2,3-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ MOP:0004167
+ has_participant: CHEBI:17483
+ S-alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glucosyl group.
+ MOP:0004172
+ MOP:0004169
+ has_participant: CHEBI:24281
+ S-glucosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosyl group.
+ MOP:0004170
+ has_participant: CHEBI:17227
+ S-D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-galactosyl-1,4beta-D-glucosyl group.
+ MOP:0004171
+ has_participant: CHEBI:20966
+ S-D-galactosyl-1,4beta-D-glucosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-galactosyl-1,4beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-glucosyl group.
+ MOP:0004173
+ has_participant: CHEBI:30684
+ S-alpha-glucosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-glucosyl group.
+ MOP:0004174
+ has_participant: CHEBI:30697
+ S-beta-glucosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-galactosyl-(1->4)-beta-D-glucosyl group.
+ MOP:0004175
+ has_participant: CHEBI:18018
+ S-D-galactosyl-(1->4)-beta-D-glucosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-galactosyl-(1->4)-beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glycosaminyl group.
+ MOP:0004176
+ has_participant: CHEBI:24399
+ S-glycosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glycosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a galactosaminyl group.
+ MOP:0004177
+ has_participant: CHEBI:24160
+ S-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-D-galactosaminyl group.
+ MOP:0004178
+ has_participant: CHEBI:21507
+ S-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0004179
+ has_participant: CHEBI:17850
+ S-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ MOP:0004180
+ has_participant: CHEBI:16565
+ S-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ MOP:0004181
+ has_participant: CHEBI:16901
+ S-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0004182
+ has_participant: CHEBI:15876
+ S-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0004183
+ has_participant: CHEBI:17723
+ S-beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ MOP:0004184
+ has_participant: CHEBI:16117
+ S-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ MOP:0004185
+ has_participant: CHEBI:22783
+ S-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0004186
+ has_participant: CHEBI:17581
+ S-N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminyl group.
+ MOP:0004187
+ has_participant: CHEBI:16250
+ S-N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminyl group.
+ MOP:0004188
+ has_participant: CHEBI:16478
+ S-N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glucosaminyl group.
+ MOP:0004189
+ has_participant: CHEBI:24272
+ S-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-D-glucosaminyl group.
+ MOP:0004190
+ has_participant: CHEBI:21524
+ S-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ MOP:0004191
+ has_participant: CHEBI:18914
+ S-1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 3-O-beta-D-galactosyl-N-acetyl-D-glucosaminyl group.
+ MOP:0004192
+ has_participant: CHEBI:18915
+ S-3-O-beta-D-galactosyl-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 3-O-beta-D-galactosyl-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ MOP:0004193
+ has_participant: CHEBI:18939
+ S-1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0004194
+ has_participant: CHEBI:17571
+ S-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0004195
+ has_participant: CHEBI:17785
+ S-alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0004196
+ has_participant: CHEBI:22381
+ S-alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminyl group.
+ MOP:0004197
+ has_participant: CHEBI:22779
+ S-beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0004198
+ has_participant: CHEBI:21580
+ S-N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0004199
+ has_participant: CHEBI:21581
+ S-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0004200
+ has_participant: CHEBI:21582
+ S-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0004201
+ has_participant: CHEBI:21583
+ S-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0004202
+ has_participant: CHEBI:16059
+ S-N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0004203
+ has_participant: CHEBI:16198
+ S-N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an iduronosyl group.
+ MOP:0004204
+ has_participant: CHEBI:24770
+ S-iduronosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an iduronosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-inosinyl group.
+ MOP:0004205
+ has_participant: CHEBI:24845
+ S-5'-inosinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-inosinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a mannosyl group.
+ MOP:0004209
+ MOP:0004206
+ has_participant: CHEBI:25171
+ S-mannosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a (N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ MOP:0004207
+ has_participant: CHEBI:18638
+ S-(N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a (N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-D-mannosyl-1,3-(r1)-beta-D-mannosyl group.
+ MOP:0004208
+ has_participant: CHEBI:22406
+ S-alpha-D-mannosyl-1,3-(r1)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-D-mannosyl-1,3-(r1)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-mannosyl group.
+ MOP:0004210
+ has_participant: CHEBI:30689
+ S-alpha-mannosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosyl group.
+ MOP:0004211
+ has_participant: CHEBI:32618
+ S-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosyl group.
+ MOP:0004212
+ has_participant: CHEBI:32890
+ S-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ MOP:0004213
+ has_participant: CHEBI:21589
+ S-N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosyl group.
+ MOP:0004214
+ has_participant: CHEBI:32601
+ S-N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosyl group.
+ MOP:0004215
+ has_participant: CHEBI:32602
+ S-N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-D-mannosyl-(1->3)-beta-D-mannosyl group.
+ MOP:0004216
+ has_participant: CHEBI:32591
+ S-alpha-D-mannosyl-(1->3)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-D-mannosyl-(1->3)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a neuraminosyl group.
+ MOP:0004217
+ has_participant: CHEBI:25509
+ S-neuraminosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a neuraminosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a neuraminoyl group.
+ MOP:0004218
+ has_participant: CHEBI:25510
+ S-neuraminoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a neuraminoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a ribosyl group.
+ MOP:0004221
+ MOP:0004219
+ has_participant: CHEBI:26566
+ S-ribosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a ribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an adenosinediphosphoribosyl group.
+ MOP:0004220
+ has_participant: CHEBI:22259
+ S-adenosinediphosphoribosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an adenosinediphosphoribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-deoxyribosyl group.
+ MOP:0004222
+ has_participant: CHEBI:30720
+ S-2-deoxyribosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-deoxyribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sialosyl group.
+ MOP:0004223
+ has_participant: CHEBI:26668
+ S-sialosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sialosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a hemicystyl group.
+ MOP:0004224
+ has_participant: CHEBI:24492
+ S-hemicystylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a hemicystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a mevalonoyl group.
+ MOP:0004225
+ has_participant: CHEBI:25353
+ S-mevalonoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a mevalonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a montanoyl group.
+ MOP:0004226
+ has_participant: CHEBI:25417
+ S-montanoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a montanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a muramyl group.
+ MOP:0004227
+ has_participant: CHEBI:25433
+ S-muramylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nucleotidyl group.
+ MOP:0004228
+ has_participant: CHEBI:25613
+ S-nucleotidylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nucleotidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-adenylyl group.
+ MOP:0004229
+ has_participant: CHEBI:22263
+ S-5'-adenylylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-adenylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-cytidylyl group.
+ MOP:0004230
+ has_participant: CHEBI:23526
+ S-5'-cytidylylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-cytidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-thymidylyl group.
+ MOP:0004231
+ has_participant: CHEBI:27003
+ S-5'-thymidylylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-thymidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-uridylyl group.
+ MOP:0004232
+ has_participant: CHEBI:27244
+ S-5'-uridylylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-uridylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-guanylyl group.
+ MOP:0004233
+ has_participant: CHEBI:24460
+ S-5'-guanylylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-guanylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-ribothymidylyl group.
+ MOP:0004234
+ has_participant: CHEBI:26569
+ S-5'-ribothymidylylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-ribothymidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-inosinylyl group.
+ MOP:0004235
+ has_participant: CHEBI:33512
+ S-5'-inosinylylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-inosinylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pantothenyl group.
+ MOP:0004236
+ has_participant: CHEBI:25850
+ S-pantothenylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pantothenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pantoyl group.
+ MOP:0004237
+ has_participant: CHEBI:25851
+ S-pantoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pantoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a peptidyl group.
+ MOP:0004238
+ has_participant: CHEBI:25907
+ S-peptidylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a peptidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phthalyl group.
+ MOP:0004239
+ has_participant: CHEBI:26096
+ S-phthalylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phthalyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a propionyl group.
+ MOP:0004240
+ has_participant: CHEBI:26294
+ S-propionylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a propionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pyruvoyl group.
+ MOP:0004241
+ has_participant: CHEBI:45360
+ S-pyruvoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pyruvoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a retinoyl group.
+ MOP:0004242
+ has_participant: CHEBI:26539
+ S-retinoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a retinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sialoyl group.
+ MOP:0004243
+ has_participant: CHEBI:26670
+ S-sialoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 3-carboxypropanoyl group.
+ MOP:0004244
+ has_participant: CHEBI:26810
+ S-3-carboxypropanoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 3-carboxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trienoyl group.
+ MOP:0004245
+ has_participant: CHEBI:27107
+ S-trienoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an anilinocarbonyl group.
+ MOP:0004246
+ has_participant: CHEBI:30692
+ S-anilinocarbonylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an anilinocarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pteroyl group.
+ MOP:0004247
+ has_participant: CHEBI:26379
+ S-pteroylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pteroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 3-carboxyprop-2-enoyl group.
+ MOP:0004248
+ has_participant: CHEBI:37953
+ S-3-carboxyprop-2-enoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a (Z)-3-carboxyprop-2-enoyl group.
+ MOP:0004249
+ has_participant: CHEBI:25122
+ S-(Z)-3-carboxyprop-2-enoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a (Z)-3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a (E)-3-carboxyprop-2-enoyl group.
+ MOP:0004250
+ has_participant: CHEBI:24126
+ S-(E)-3-carboxyprop-2-enoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a (E)-3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2,6-dichlorobenzoyl group.
+ MOP:0004251
+ has_participant: CHEBI:48625
+ S-2,6-dichlorobenzoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2,6-dichlorobenzoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-muramyl group.
+ MOP:0004252
+ has_participant: CHEBI:30701
+ S-alpha-muramylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-muramyl group.
+ MOP:0004253
+ has_participant: CHEBI:30702
+ S-beta-muramylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a beta-muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a dihydrolipoyl group.
+ MOP:0004254
+ has_participant: CHEBI:50488
+ S-dihydrolipoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sinapoyl group.
+ MOP:0004255
+ has_participant: CHEBI:50561
+ S-sinapoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sinapoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carboxyacetyl group.
+ MOP:0004256
+ has_participant: CHEBI:50650
+ S-carboxyacetylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carboxyacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a divalent carboacyl group.
+ MOP:0004257
+ has_participant: CHEBI:23855
+ S-divalent carboacylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a divalent carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an aspartoyl group.
+ MOP:0004258
+ has_participant: CHEBI:22663
+ S-aspartoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-aspartoyl group.
+ MOP:0004259
+ has_participant: CHEBI:32464
+ S-L-aspartoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-aspartoyl group.
+ MOP:0004260
+ has_participant: CHEBI:32468
+ S-D-aspartoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a citraconoyl group.
+ MOP:0004261
+ has_participant: CHEBI:23315
+ S-citraconoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a citraconoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glutamoyl group.
+ MOP:0004262
+ has_participant: CHEBI:24322
+ S-glutamoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-glutamoyl group.
+ MOP:0004263
+ has_participant: CHEBI:32481
+ S-D-glutamoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-glutamoyl group.
+ MOP:0004264
+ has_participant: CHEBI:32475
+ S-L-glutamoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a maloyl group.
+ MOP:0004265
+ has_participant: CHEBI:25138
+ S-maloylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a maloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phthaloyl group.
+ MOP:0004266
+ has_participant: CHEBI:26095
+ S-phthaloylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phthaloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a succinyl group.
+ MOP:0004267
+ has_participant: CHEBI:37952
+ S-succinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a succinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a butenedioyl group.
+ MOP:0004268
+ has_participant: CHEBI:37954
+ S-butenedioylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a butenedioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a fumaroyl group.
+ MOP:0004269
+ has_participant: CHEBI:24125
+ S-fumaroylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a fumaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a maleoyl group.
+ MOP:0004270
+ has_participant: CHEBI:25121
+ S-maleoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a maleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a hexanedioyl group.
+ MOP:0004271
+ has_participant: CHEBI:48082
+ S-hexanedioylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a hexanedioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a malonyl group.
+ MOP:0004272
+ has_participant: CHEBI:25134
+ S-malonylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a malonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an ornithyl group.
+ MOP:0004273
+ has_participant: CHEBI:46929
+ S-ornithylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an ornithyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-ornithyl group.
+ MOP:0004274
+ has_participant: CHEBI:44700
+ S-L-ornithylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-ornithyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a half-cystyl group.
+ MOP:0004275
+ has_participant: CHEBI:30770
+ S-half-cystylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a half-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-tyrosin-O(4)-yl group.
+ MOP:0004276
+ has_participant: CHEBI:32768
+ S-L-tyrosin-O(4)-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-threonin-O(3)-yl group.
+ MOP:0004277
+ has_participant: CHEBI:32825
+ S-L-threonin-O(3)-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an L-threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-tyrosin-O(4)-yl group.
+ MOP:0004278
+ has_participant: CHEBI:32780
+ S-D-tyrosin-O(4)-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-threonin-O(3)-yl group.
+ MOP:0004279
+ has_participant: CHEBI:32831
+ S-D-threonin-O(3)-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a D-threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tyrosin-O(4)-yl group.
+ MOP:0004280
+ has_participant: CHEBI:32788
+ S-tyrosin-O(4)-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a threonin-O(3)-yl group.
+ MOP:0004281
+ has_participant: CHEBI:26985
+ S-threonin-O(3)-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an oxalyl group.
+ MOP:0004282
+ has_participant: CHEBI:30870
+ S-oxalylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an oxalyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a fumagillin-2-yl group.
+ MOP:0004283
+ has_participant: CHEBI:42601
+ S-fumagillin-2-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a fumagillin-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acetoacetyl group.
+ MOP:0004284
+ has_participant: CHEBI:48051
+ S-acetoacetylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acetoacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-linolenoyl group.
+ MOP:0004285
+ has_participant: CHEBI:32388
+ S-alpha-linolenoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alpha-linolenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a gamma-linolenoyl group.
+ MOP:0004286
+ has_participant: CHEBI:32390
+ S-gamma-linolenoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a gamma-linolenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carbamimidoyl group.
+ MOP:0004287
+ has_participant: CHEBI:48090
+ S-carbamimidoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carbamimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a formimidoyl group.
+ MOP:0004288
+ has_participant: CHEBI:24084
+ S-formimidoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a formimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trifluoroacetyl group.
+ MOP:0004289
+ has_participant: CHEBI:45888
+ S-trifluoroacetylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trifluoroacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carboxymethyl group.
+ MOP:0004290
+ has_participant: CHEBI:41402
+ S-carboxymethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carboxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a methylenecarbonyl group.
+ MOP:0004291
+ has_participant: CHEBI:43923
+ S-methylenecarbonylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a methylenecarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-hydroxyacetimidoyl group.
+ MOP:0004292
+ has_participant: CHEBI:48055
+ S-N-hydroxyacetimidoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-hydroxyacetimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acryloyl group.
+ MOP:0004293
+ has_participant: CHEBI:48077
+ S-acryloylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acryloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tert-butoxycarbonyl group.
+ MOP:0004294
+ has_participant: CHEBI:48502
+ S-tert-butoxycarbonylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tert-butoxycarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfanediyl group.
+ MOP:0004295
+ has_participant: CHEBI:29830
+ S-sulfanediylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phenylsulfanyl group.
+ MOP:0004296
+ has_participant: CHEBI:48499
+ S-phenylsulfanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phenylsulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a methylsulfanyl group.
+ MOP:0004297
+ has_participant: CHEBI:48563
+ S-methylsulfanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a methylsulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfaniumyl group.
+ MOP:0004298
+ has_participant: CHEBI:36945
+ S-sulfaniumylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a disulfanidyl group.
+ MOP:0004299
+ has_participant: CHEBI:29838
+ S-disulfanidylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a disulfanidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a disulfanediyl group.
+ MOP:0004300
+ has_participant: CHEBI:29826
+ S-disulfanediylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a disulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a disulfanyl group.
+ MOP:0004301
+ has_participant: CHEBI:30605
+ S-disulfanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a disulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tetrasulfanyl group.
+ MOP:0004302
+ has_participant: CHEBI:30607
+ S-tetrasulfanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tetrasulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tetrasulfanediyl group.
+ MOP:0004303
+ has_participant: CHEBI:29836
+ S-tetrasulfanediylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tetrasulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trisulfanyl group.
+ MOP:0004304
+ has_participant: CHEBI:30606
+ S-trisulfanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trisulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trisulfanediyl group.
+ MOP:0004305
+ has_participant: CHEBI:29834
+ S-trisulfanediylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trisulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pentasulfanyl group.
+ MOP:0004306
+ has_participant: CHEBI:30608
+ S-pentasulfanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pentasulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a diselanyl group.
+ MOP:0004307
+ has_participant: CHEBI:30602
+ S-diselanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a diselanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tellanyl group.
+ MOP:0004308
+ has_participant: CHEBI:30458
+ S-tellanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tellanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tellanediyl group.
+ MOP:0004309
+ has_participant: CHEBI:30455
+ S-tellanediylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tellanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tellaniumyl group.
+ MOP:0004310
+ has_participant: CHEBI:30447
+ S-tellaniumylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tellaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a ditellanyl group.
+ MOP:0004311
+ has_participant: CHEBI:30601
+ S-ditellanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a ditellanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an amidyl group.
+ MOP:0004312
+ has_participant: CHEBI:48373
+ S-amidylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an amidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an azanediyl group.
+ MOP:0004313
+ has_participant: CHEBI:29343
+ S-azanediylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an azanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-aminoethyl group.
+ MOP:0004314
+ has_participant: CHEBI:22502
+ S-2-aminoethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-aminoethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 4-aminobutyl group.
+ MOP:0004315
+ has_participant: CHEBI:50339
+ S-4-aminobutylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 4-aminobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an azanetriyl group.
+ MOP:0004316
+ has_participant: CHEBI:30228
+ S-azanetriylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an azanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a hydrazine-1,2-diyl group.
+ MOP:0004317
+ has_participant: CHEBI:30098
+ S-hydrazine-1,2-diylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a hydrazine-1,2-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a diazyn-1-ium-1-yl group.
+ MOP:0004318
+ has_participant: CHEBI:30108
+ S-diazyn-1-ium-1-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a diazyn-1-ium-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phosphanetriyl group.
+ MOP:0004319
+ has_participant: CHEBI:30206
+ S-phosphanetriylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phosphanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phosphanediyl group.
+ MOP:0004320
+ has_participant: CHEBI:29944
+ S-phosphanediylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phosphanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phosphanyl group.
+ MOP:0004321
+ has_participant: CHEBI:29936
+ S-phosphanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phosphanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a lambda(5)-phosphanyl group.
+ MOP:0004322
+ has_participant: CHEBI:30284
+ S-lambda(5)-phosphanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a lambda(5)-phosphanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phosphaniumyl group.
+ MOP:0004323
+ has_participant: CHEBI:30279
+ S-phosphaniumylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phosphaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arsanyl group.
+ MOP:0004324
+ has_participant: CHEBI:29759
+ S-arsanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arsanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arsanediyl group.
+ MOP:0004325
+ has_participant: CHEBI:29763
+ S-arsanediylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arsanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arsanetriyl group.
+ MOP:0004326
+ has_participant: CHEBI:29766
+ S-arsanetriylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arsanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arsaniumyl group.
+ MOP:0004327
+ has_participant: CHEBI:29842
+ S-arsaniumylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arsaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a lambda(5)-arsanyl group.
+ MOP:0004328
+ has_participant: CHEBI:30273
+ S-lambda(5)-arsanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a lambda(5)-arsanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a stibaniumyl group.
+ MOP:0004329
+ has_participant: CHEBI:30291
+ S-stibaniumylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a stibaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a lambda(5)-stibanyl group.
+ MOP:0004330
+ has_participant: CHEBI:30293
+ S-lambda(5)-stibanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a lambda(5)-stibanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a boranyl group.
+ MOP:0004331
+ has_participant: CHEBI:33604
+ S-boranylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a boranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a boranetriyl group.
+ MOP:0004332
+ has_participant: CHEBI:30169
+ S-boranetriylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a boranetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a boranediyl group.
+ MOP:0004333
+ has_participant: CHEBI:38988
+ S-boranediylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a boranediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a boranuidyl group.
+ MOP:0004334
+ has_participant: CHEBI:30159
+ S-boranuidylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a boranuidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a germyl group.
+ MOP:0004335
+ has_participant: CHEBI:30542
+ S-germylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a germyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a germanediyl group.
+ MOP:0004336
+ has_participant: CHEBI:30554
+ S-germanediylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a germanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a germanetetrayl group.
+ MOP:0004337
+ has_participant: CHEBI:30547
+ S-germanetetraylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a germanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a germanetriyl group.
+ MOP:0004338
+ has_participant: CHEBI:30544
+ S-germanetriylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a germanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a silyl group.
+ MOP:0004339
+ has_participant: CHEBI:30541
+ S-silylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a silyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a silanediyl group.
+ MOP:0004340
+ has_participant: CHEBI:30587
+ S-silanediylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a silanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a silanetriyl group.
+ MOP:0004341
+ has_participant: CHEBI:30576
+ S-silanetriylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a silanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a silanetetrayl group.
+ MOP:0004342
+ has_participant: CHEBI:30583
+ S-silanetetraylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a silanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a disilanyl group.
+ MOP:0004343
+ has_participant: CHEBI:30594
+ S-disilanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a disilanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alumanyl group.
+ MOP:0004344
+ has_participant: CHEBI:30135
+ S-alumanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alumanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a stannyl group.
+ MOP:0004345
+ has_participant: CHEBI:30540
+ S-stannylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a stannyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a stannanetriyl group.
+ MOP:0004346
+ has_participant: CHEBI:30575
+ S-stannanetriylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a stannanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a plumbanetriyl group.
+ MOP:0004347
+ has_participant: CHEBI:30577
+ S-plumbanetriylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a plumbanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a plumbyl group.
+ MOP:0004348
+ has_participant: CHEBI:30543
+ S-plumbylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a plumbyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a gallanyl group.
+ MOP:0004349
+ has_participant: CHEBI:37119
+ S-gallanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a gallanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an indiganyl group.
+ MOP:0004350
+ has_participant: CHEBI:30431
+ S-indiganylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an indiganyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a thallanyl group.
+ MOP:0004351
+ has_participant: CHEBI:30442
+ S-thallanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a thallanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phosphatidyl group.
+ MOP:0004352
+ has_participant: CHEBI:26025
+ S-phosphatidylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phosphatidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nucleosidyl group.
+ MOP:0004353
+ has_participant: CHEBI:33494
+ S-nucleosidylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nucleosidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a guanosyl group.
+ MOP:0004354
+ has_participant: CHEBI:24459
+ S-guanosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a guanosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an inosyl group.
+ MOP:0004355
+ has_participant: CHEBI:24849
+ S-inosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an inosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a thymidyl group.
+ MOP:0004356
+ has_participant: CHEBI:27002
+ S-thymidylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a thymidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an adenosyl group.
+ MOP:0004357
+ has_participant: CHEBI:33505
+ S-adenosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an adenosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-adenosyl group.
+ MOP:0004358
+ has_participant: CHEBI:22261
+ S-5'-adenosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 5'-adenosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an uridyl group.
+ MOP:0004359
+ has_participant: CHEBI:27243
+ S-uridylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an uridyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cytidyl group.
+ MOP:0004360
+ has_participant: CHEBI:23525
+ S-cytidylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cytidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a dolichyl group.
+ MOP:0004361
+ has_participant: CHEBI:23883
+ S-dolichylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a dolichyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-trans,6-trans-farnesyl group.
+ MOP:0004362
+ has_participant: CHEBI:36535
+ S-2-trans,6-trans-farnesylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-trans,6-trans-farnesyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a margaryl group.
+ MOP:0004363
+ has_participant: CHEBI:32925
+ S-margarylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a margaryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a methyl group.
+ MOP:0004364
+ has_participant: CHEBI:32875
+ S-methylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a methyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a methanetetrayl group.
+ MOP:0004365
+ has_participant: CHEBI:30039
+ S-methanetetraylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a methanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a methanetriyl group.
+ MOP:0004366
+ has_participant: CHEBI:29433
+ S-methanetriylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a methanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trichloromethyl group.
+ MOP:0004367
+ has_participant: CHEBI:30736
+ S-trichloromethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trichloromethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trifluoromethyl group.
+ MOP:0004368
+ has_participant: CHEBI:50127
+ S-trifluoromethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trifluoromethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alkyl group.
+ MOP:0004369
+ has_participant: CHEBI:22323
+ S-alkylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a butyl group.
+ MOP:0004370
+ has_participant: CHEBI:41264
+ S-butylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a ceryl group.
+ MOP:0004371
+ has_participant: CHEBI:23081
+ S-cerylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a ceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a decyl group.
+ MOP:0004372
+ has_participant: CHEBI:23580
+ S-decylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a decyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a dodecyl group.
+ MOP:0004373
+ has_participant: CHEBI:23870
+ S-dodecylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a dodecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a heptyl group.
+ MOP:0004374
+ has_participant: CHEBI:24526
+ S-heptylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a heptyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a hexyl group.
+ MOP:0004375
+ has_participant: CHEBI:24593
+ S-hexylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a hexyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a myricyl group.
+ MOP:0004376
+ has_participant: CHEBI:25453
+ S-myricylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a myricyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a myristyl group.
+ MOP:0004377
+ has_participant: CHEBI:25457
+ S-myristylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a myristyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nonyl group.
+ MOP:0004378
+ has_participant: CHEBI:25589
+ S-nonylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an octyl group.
+ MOP:0004379
+ has_participant: CHEBI:25657
+ S-octylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an octyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a palmityl group.
+ MOP:0004380
+ has_participant: CHEBI:25842
+ S-palmitylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a palmityl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pentyl group.
+ MOP:0004381
+ has_participant: CHEBI:25902
+ S-pentylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a propyl group.
+ MOP:0004382
+ has_participant: CHEBI:26308
+ S-propylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a propyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a stearyl group.
+ MOP:0004383
+ has_participant: CHEBI:26755
+ S-stearylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a stearyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an isopropyl group.
+ MOP:0004384
+ has_participant: CHEBI:30353
+ S-isopropylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an isopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an ethyl group.
+ MOP:0004385
+ has_participant: CHEBI:37807
+ S-ethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an ethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an isobutyl group.
+ MOP:0004386
+ has_participant: CHEBI:30356
+ S-isobutylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an isobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pentan-2-yl group.
+ MOP:0004387
+ has_participant: CHEBI:32880
+ S-pentan-2-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pentan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an isopentyl group.
+ MOP:0004388
+ has_participant: CHEBI:30359
+ S-isopentylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an isopentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 3-methylbutan-2-yl group.
+ MOP:0004389
+ has_participant: CHEBI:32882
+ S-3-methylbutan-2-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 3-methylbutan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tert-pentyl group.
+ MOP:0004390
+ has_participant: CHEBI:30360
+ S-tert-pentylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tert-pentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a neopentyl group.
+ MOP:0004391
+ has_participant: CHEBI:30357
+ S-neopentylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a neopentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an undecyl group.
+ MOP:0004392
+ has_participant: CHEBI:32900
+ S-undecylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an undecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tridecyl group.
+ MOP:0004393
+ has_participant: CHEBI:32908
+ S-tridecylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tridecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pentadecyl group.
+ MOP:0004394
+ has_participant: CHEBI:32909
+ S-pentadecylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pentadecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nonadecyl group.
+ MOP:0004395
+ has_participant: CHEBI:32928
+ S-nonadecylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nonadecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arachidyl group.
+ MOP:0004396
+ has_participant: CHEBI:32930
+ S-arachidylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arachidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a henicosyl group.
+ MOP:0004397
+ has_participant: CHEBI:32932
+ S-henicosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a henicosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a behenyl group.
+ MOP:0004398
+ has_participant: CHEBI:32933
+ S-behenylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a behenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tricosyl group.
+ MOP:0004399
+ has_participant: CHEBI:32935
+ S-tricosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tricosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a lignoceryl group.
+ MOP:0004400
+ has_participant: CHEBI:32937
+ S-lignocerylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a lignoceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pentacosyl group.
+ MOP:0004401
+ has_participant: CHEBI:32939
+ S-pentacosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pentacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a heptacosyl group.
+ MOP:0004402
+ has_participant: CHEBI:32942
+ S-heptacosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a heptacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a montanyl group.
+ MOP:0004403
+ has_participant: CHEBI:32944
+ S-montanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a montanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nonacosyl group.
+ MOP:0004404
+ has_participant: CHEBI:32945
+ S-nonacosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nonacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sec-butyl group.
+ MOP:0004405
+ has_participant: CHEBI:45557
+ S-sec-butylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sec-butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tert-butyl group.
+ MOP:0004406
+ has_participant: CHEBI:30355
+ S-tert-butylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tert-butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pentan-3-yl group.
+ MOP:0004407
+ has_participant: CHEBI:32881
+ S-pentan-3-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a pentan-3-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-chloroethyl group.
+ MOP:0004408
+ has_participant: CHEBI:47553
+ S-2-chloroethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-chloroethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 1-chloroethyl group.
+ MOP:0004409
+ has_participant: CHEBI:48099
+ S-1-chloroethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 1-chloroethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a hydrocarbyl group.
+ MOP:0004410
+ has_participant: CHEBI:33248
+ S-hydrocarbylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a hydrocarbyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an aryl group.
+ MOP:0004411
+ has_participant: CHEBI:33338
+ S-arylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an aryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phenyl group.
+ MOP:0004412
+ has_participant: CHEBI:30396
+ S-phenylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a biphenyl-4-yl group.
+ MOP:0004413
+ has_participant: CHEBI:35447
+ S-biphenyl-4-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a biphenyl-4-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a naphthyl group.
+ MOP:0004414
+ has_participant: CHEBI:51140
+ S-naphthylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 1-naphthyl group.
+ MOP:0004415
+ has_participant: CHEBI:51138
+ S-1-naphthylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 1-naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-naphthyl group.
+ MOP:0004416
+ has_participant: CHEBI:51139
+ S-2-naphthylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cycloalkyl group.
+ MOP:0004417
+ has_participant: CHEBI:33441
+ S-cycloalkylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cycloalkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cyclobutyl group.
+ MOP:0004418
+ has_participant: CHEBI:30376
+ S-cyclobutylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cyclobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cyclopropyl group.
+ MOP:0004419
+ has_participant: CHEBI:30364
+ S-cyclopropylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cyclopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alkenyl group.
+ MOP:0004420
+ has_participant: CHEBI:37614
+ S-alkenylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alkenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an oleyl group.
+ MOP:0004421
+ has_participant: CHEBI:25670
+ S-oleylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an oleyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an allyl group.
+ MOP:0004422
+ has_participant: CHEBI:30361
+ S-allylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an allyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an isopropenyl group.
+ MOP:0004423
+ has_participant: CHEBI:30354
+ S-isopropenylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an isopropenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a vinyl group.
+ MOP:0004424
+ has_participant: CHEBI:37603
+ S-vinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a vinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a prenyl group.
+ MOP:0004427
+ MOP:0004425
+ has_participant: CHEBI:26248
+ S-prenylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a prenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phytyl group.
+ MOP:0004426
+ has_participant: CHEBI:26126
+ S-phytylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phytyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a polyprenyl group.
+ MOP:0004428
+ has_participant: CHEBI:26201
+ S-polyprenylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a polyprenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a farnesyl group.
+ MOP:0004429
+ has_participant: CHEBI:24017
+ S-farnesylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a farnesyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a geranyl group.
+ MOP:0004430
+ has_participant: CHEBI:24224
+ S-geranylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a geranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a geranylgeranyl group.
+ MOP:0004431
+ has_participant: CHEBI:24231
+ S-geranylgeranylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a geranylgeranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a retinyl group.
+ MOP:0004432
+ has_participant: CHEBI:26541
+ S-retinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a retinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an adamantan-2-yl group.
+ MOP:0004433
+ has_participant: CHEBI:48078
+ S-adamantan-2-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an adamantan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cycloalkenyl group.
+ MOP:0004434
+ has_participant: CHEBI:48886
+ S-cycloalkenylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cycloalkenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a campholenic cyclohexenyl group.
+ MOP:0004435
+ has_participant: CHEBI:48885
+ S-campholenic cyclohexenylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a campholenic cyclohexenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cyclopentadienyl group.
+ MOP:0004436
+ has_participant: CHEBI:30663
+ S-cyclopentadienylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an eta(5)-cyclopentadienyl group.
+ MOP:0004437
+ has_participant: CHEBI:36763
+ S-eta(5)-cyclopentadienylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an eta(5)-cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an eta(1)-cyclopentadienyl group.
+ MOP:0004438
+ has_participant: CHEBI:36764
+ S-eta(1)-cyclopentadienylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an eta(1)-cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an ethene-1,2-diyl group.
+ MOP:0004439
+ has_participant: CHEBI:46880
+ S-ethene-1,2-diylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an ethene-1,2-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arachidonyl group.
+ MOP:0004440
+ has_participant: CHEBI:22612
+ S-arachidonylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arachidonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a benzyl group.
+ MOP:0004441
+ has_participant: CHEBI:22744
+ S-benzylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a benzyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an anthracen-1-yl group.
+ MOP:0004442
+ has_participant: CHEBI:48287
+ S-anthracen-1-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an anthracen-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an anthracen-2-yl group.
+ MOP:0004443
+ has_participant: CHEBI:48371
+ S-anthracen-2-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an anthracen-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an imidazolyl group.
+ MOP:0004444
+ has_participant: CHEBI:50052
+ S-imidazolylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an imidazolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an imidazol-1-yl group.
+ MOP:0004445
+ has_participant: CHEBI:50053
+ S-imidazol-1-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an imidazol-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an imidazol-2-yl group.
+ MOP:0004446
+ has_participant: CHEBI:50054
+ S-imidazol-2-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an imidazol-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an imidazol-5-yl group.
+ MOP:0004447
+ has_participant: CHEBI:50055
+ S-imidazol-5-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an imidazol-5-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an imidazol-4-yl group.
+ MOP:0004448
+ has_participant: CHEBI:50056
+ S-imidazol-4-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an imidazol-4-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a furyl group.
+ MOP:0004449
+ has_participant: CHEBI:24131
+ S-furylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-furyl group.
+ MOP:0004450
+ has_participant: CHEBI:19586
+ S-2-furylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 3-furyl group.
+ MOP:0004451
+ has_participant: CHEBI:20025
+ S-3-furylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 3-furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a thienyl group.
+ MOP:0004452
+ has_participant: CHEBI:37991
+ S-thienylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-thienyl group.
+ MOP:0004453
+ has_participant: CHEBI:35849
+ S-2-thienylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 3-thienyl group.
+ MOP:0004454
+ has_participant: CHEBI:37992
+ S-3-thienylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 3-thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an adenin-9-yl group.
+ MOP:0004455
+ has_participant: CHEBI:30756
+ S-adenin-9-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an adenin-9-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a guanin-9-yl group.
+ MOP:0004456
+ has_participant: CHEBI:30755
+ S-guanin-9-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a guanin-9-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acetimidoyl group.
+ MOP:0004457
+ has_participant: CHEBI:48050
+ S-acetimidoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acetimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an organyl group.
+ MOP:0004458
+ has_participant: CHEBI:33249
+ S-organylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an organyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an organic heterocyclyl group.
+ MOP:0004459
+ has_participant: CHEBI:33453
+ S-organic heterocyclylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an organic heterocyclyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a heteroaryl group.
+ MOP:0004460
+ has_participant: CHEBI:33470
+ S-heteroarylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a heteroaryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 4,4'-dimethoxytriphenylmethyl group.
+ MOP:0004461
+ has_participant: CHEBI:51095
+ S-4,4'-dimethoxytriphenylmethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 4,4'-dimethoxytriphenylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tauryl group.
+ MOP:0004462
+ has_participant: CHEBI:26861
+ S-taurylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tauryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a triflyl group.
+ MOP:0004463
+ has_participant: CHEBI:48548
+ S-triflylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a triflyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glycidyl group.
+ MOP:0004464
+ has_participant: CHEBI:24366
+ S-glycidylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a glycidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfanylmethyl group.
+ MOP:0004465
+ has_participant: CHEBI:50326
+ S-sulfanylmethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfanylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a selanylmethyl group.
+ MOP:0004466
+ has_participant: CHEBI:50327
+ S-selanylmethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a selanylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-carboxyethyl group.
+ MOP:0004467
+ has_participant: CHEBI:50329
+ S-2-carboxyethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-carboxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-amino-2-oxoethyl group.
+ MOP:0004468
+ has_participant: CHEBI:50330
+ S-2-amino-2-oxoethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-amino-2-oxoethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 3-amino-3-oxopropyl group.
+ MOP:0004469
+ has_participant: CHEBI:50331
+ S-3-amino-3-oxopropylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 3-amino-3-oxopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-(methylsulfanyl)ethyl group.
+ MOP:0004470
+ has_participant: CHEBI:50332
+ S-2-(methylsulfanyl)ethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-(methylsulfanyl)ethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 4-hydroxybenzyl group.
+ MOP:0004471
+ has_participant: CHEBI:50336
+ S-4-hydroxybenzylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 4-hydroxybenzyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 1H-indol-3-ylmethyl group.
+ MOP:0004472
+ has_participant: CHEBI:50337
+ S-1H-indol-3-ylmethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 1H-indol-3-ylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 1H-imidazol-4-ylmethyl group.
+ MOP:0004473
+ has_participant: CHEBI:50338
+ S-1H-imidazol-4-ylmethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 1H-imidazol-4-ylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 3-carbamimidamidopropyl group.
+ MOP:0004474
+ has_participant: CHEBI:50340
+ S-3-carbamimidamidopropylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 3-carbamimidamidopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a hydroxymethyl group.
+ MOP:0004475
+ has_participant: CHEBI:24712
+ S-hydroxymethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a hydroxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 1-hydroxyethyl group.
+ MOP:0004476
+ has_participant: CHEBI:50341
+ S-1-hydroxyethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 1-hydroxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a haloalkyl group.
+ MOP:0004477
+ has_participant: CHEBI:50491
+ S-haloalkylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a haloalkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-(trimethylsilyl)ethoxymethyl group.
+ MOP:0004478
+ has_participant: CHEBI:51093
+ S-2-(trimethylsilyl)ethoxymethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-(trimethylsilyl)ethoxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acyl group.
+ MOP:0004479
+ has_participant: CHEBI:22221
+ S-acylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an organoheteryl group.
+ MOP:0004480
+ has_participant: CHEBI:33456
+ S-organoheterylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an organoheteryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an oxalosulfanyl group.
+ MOP:0004481
+ has_participant: CHEBI:30874
+ S-oxalosulfanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an oxalosulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an organosilyl group.
+ MOP:0004482
+ has_participant: CHEBI:33478
+ S-organosilylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an organosilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trimethylsilyl group.
+ MOP:0004483
+ has_participant: CHEBI:51088
+ S-trimethylsilylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trimethylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a triisopropylsilyl group.
+ MOP:0004484
+ has_participant: CHEBI:51089
+ S-triisopropylsilylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a triisopropylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tert-butyldiphenylsilyl group.
+ MOP:0004485
+ has_participant: CHEBI:51090
+ S-tert-butyldiphenylsilylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tert-butyldiphenylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tert-butyldimethylsilyl group.
+ MOP:0004486
+ has_participant: CHEBI:51091
+ S-tert-butyldimethylsilylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tert-butyldimethylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a thioacyl group.
+ MOP:0004487
+ has_participant: CHEBI:49063
+ S-thioacylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a thioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carbothioacyl group.
+ MOP:0004488
+ has_participant: CHEBI:49066
+ S-carbothioacylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an univalent carbothioacyl group.
+ MOP:0004489
+ has_participant: CHEBI:49067
+ S-univalent carbothioacylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an univalent carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a divalent carbothioacyl group.
+ MOP:0004490
+ has_participant: CHEBI:49068
+ S-divalent carbothioacylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a divalent carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carbonimidoyl group.
+ MOP:0004491
+ has_participant: CHEBI:29815
+ S-carbonimidoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carbonimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a thiocarbonyl group.
+ MOP:0004492
+ has_participant: CHEBI:30256
+ S-thiocarbonylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a thiocarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a (fluoren-9-ylmethoxy)carbonyl group.
+ MOP:0004493
+ has_participant: CHEBI:48605
+ S-(fluoren-9-ylmethoxy)carbonylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a (fluoren-9-ylmethoxy)carbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carbonyl group.
+ MOP:0004494
+ has_participant: CHEBI:23019
+ S-carbonylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a carbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cytosin-1-yl group.
+ MOP:0004495
+ has_participant: CHEBI:30758
+ S-cytosin-1-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a cytosin-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a thymin-1-yl group.
+ MOP:0004496
+ has_participant: CHEBI:30757
+ S-thymin-1-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a thymin-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an uracil-1-yl group.
+ MOP:0004497
+ has_participant: CHEBI:30759
+ S-uracil-1-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an uracil-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a morpholin-4-ylsulfonyl group.
+ MOP:0004498
+ has_participant: CHEBI:45701
+ S-morpholin-4-ylsulfonylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a morpholin-4-ylsulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acetohydrazonoyl group.
+ MOP:0004499
+ has_participant: CHEBI:48054
+ S-acetohydrazonoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acetohydrazonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-hydroxyethyl group.
+ MOP:0004500
+ has_participant: CHEBI:44730
+ S-2-hydroxyethylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a 2-hydroxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an aminosulfinyl group.
+ MOP:0004501
+ has_participant: CHEBI:48257
+ S-aminosulfinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an aminosulfinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a disiloxanyl group.
+ MOP:0004502
+ has_participant: CHEBI:48142
+ S-disiloxanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a disiloxanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a disiloxane-1,3-diyl group.
+ MOP:0004503
+ has_participant: CHEBI:48143
+ S-disiloxane-1,3-diylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a disiloxane-1,3-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an azinoyl group.
+ MOP:0004504
+ has_participant: CHEBI:29771
+ S-azinoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an azinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an azonoyl group.
+ MOP:0004505
+ has_participant: CHEBI:37768
+ S-azonoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an azonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phosphorothioyl group.
+ MOP:0004506
+ has_participant: CHEBI:32412
+ S-phosphorothioylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phosphorothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phosphonothioyl group.
+ MOP:0004507
+ has_participant: CHEBI:32413
+ S-phosphonothioylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phosphonothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arsonoyl group.
+ MOP:0004508
+ has_participant: CHEBI:29848
+ S-arsonoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arsonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arsinoyl group.
+ MOP:0004509
+ has_participant: CHEBI:30277
+ S-arsinoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arsinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a stiboryl group.
+ MOP:0004510
+ has_participant: CHEBI:48439
+ S-stiborylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a stiboryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfamoyl group.
+ MOP:0004511
+ has_participant: CHEBI:48266
+ S-sulfamoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a S-aminosulfinimidoyl group.
+ MOP:0004512
+ has_participant: CHEBI:48254
+ S-S-aminosulfinimidoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a S-aminosulfinimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a S-aminosulfonimidoyl group.
+ MOP:0004513
+ has_participant: CHEBI:48264
+ S-S-aminosulfonimidoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a S-aminosulfonimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a chloryl group.
+ MOP:0004514
+ has_participant: CHEBI:29883
+ S-chlorylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a chloryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a chlorosyl group.
+ MOP:0004515
+ has_participant: CHEBI:29878
+ S-chlorosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a chlorosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a perchloryl group.
+ MOP:0004516
+ has_participant: CHEBI:29877
+ S-perchlorylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a perchloryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a bromosyl group.
+ MOP:0004517
+ has_participant: CHEBI:29871
+ S-bromosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a bromosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a bromyl group.
+ MOP:0004518
+ has_participant: CHEBI:29881
+ S-bromylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a bromyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a perbromyl group.
+ MOP:0004519
+ has_participant: CHEBI:29891
+ S-perbromylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a perbromyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an iodosyl group.
+ MOP:0004520
+ has_participant: CHEBI:29897
+ S-iodosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an iodosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an iodyl group.
+ MOP:0004521
+ has_participant: CHEBI:29904
+ S-iodylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an iodyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a periodyl group.
+ MOP:0004522
+ has_participant: CHEBI:29908
+ S-periodylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a periodyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a fluorosyl group.
+ MOP:0004523
+ has_participant: CHEBI:30241
+ S-fluorosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a fluorosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfonyl group.
+ MOP:0004539
+ MOP:0004524
+ has_participant: CHEBI:29825
+ S-sulfonylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acetoxysulfonyl group.
+ MOP:0004525
+ has_participant: CHEBI:48065
+ S-acetoxysulfonylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an acetoxysulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfonothioyl group.
+ MOP:0004526
+ has_participant: CHEBI:29828
+ S-sulfonothioylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfonothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfinothioyl group.
+ MOP:0004527
+ has_participant: CHEBI:29827
+ S-sulfinothioylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfinothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfonodithioyl group.
+ MOP:0004528
+ has_participant: CHEBI:29835
+ S-sulfonodithioylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfonodithioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trioxidanyl group.
+ MOP:0004529
+ has_participant: CHEBI:29791
+ S-trioxidanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trioxidanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trioxidanediyl group.
+ MOP:0004530
+ has_participant: CHEBI:30493
+ S-trioxidanediylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a trioxidanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a heterocyclyl group.
+ MOP:0004531
+ has_participant: CHEBI:48271
+ S-heterocyclylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a heterocyclyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phosphoramidochloridoyl group.
+ MOP:0004532
+ has_participant: CHEBI:48229
+ S-phosphoramidochloridoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a phosphoramidochloridoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a S-aminosulfonodiimidoyl group.
+ MOP:0004533
+ has_participant: CHEBI:48265
+ S-S-aminosulfonodiimidoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a S-aminosulfonodiimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an aminosulfanyl group.
+ MOP:0004534
+ has_participant: CHEBI:48252
+ S-aminosulfanylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an aminosulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfinyl group.
+ MOP:0004535
+ has_participant: CHEBI:29822
+ S-sulfinylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arsoryl group.
+ MOP:0004536
+ has_participant: CHEBI:30274
+ S-arsorylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an arsoryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an azanediidyl group.
+ MOP:0004537
+ has_participant: CHEBI:30227
+ S-azanediidylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an azanediidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfinimidoyl group.
+ MOP:0004538
+ has_participant: CHEBI:29829
+ S-sulfinimidoylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfinimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tosyl group.
+ MOP:0004540
+ has_participant: CHEBI:51094
+ S-tosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a tosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a brosyl group.
+ MOP:0004541
+ has_participant: CHEBI:51101
+ S-brosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a brosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nosyl group.
+ MOP:0004542
+ has_participant: CHEBI:51102
+ S-nosylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an indolyl group.
+ MOP:0004544
+ has_participant: CHEBI:51609
+ S-indolylamination
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an indolyl group.
+ RSC:xp
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an indol-1-yl group.
+ MOP:0004545
+ has_participant: CHEBI:51610
+ S-indol-1-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an indol-1-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an indol-2-yl group.
+ MOP:0004546
+ has_participant: CHEBI:51611
+ S-indol-2-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an indol-2-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an indol-3-yl group.
+ MOP:0004547
+ has_participant: CHEBI:51612
+ S-indol-3-ylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an indol-3-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-oxindolyl group.
+ MOP:0004548
+ has_participant: CHEBI:51613
+ S-N-oxindolylation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an N-oxindolyl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alkylamino group.
+ MOP:0004549
+ has_participant: CHEBI:22332
+ S-alkylamination
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an alkylamino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a halo group.
+ MOP:0004550
+ has_participant: CHEBI:47854
+ S-halogenation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a halo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a bromo group.
+ MOP:0004551
+ has_participant: CHEBI:47265
+ S-bromination
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a bromo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a chloro group.
+ MOP:0004552
+ has_participant: CHEBI:47853
+ S-chlorination
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a chloro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a fluoro group.
+ MOP:0004553
+ has_participant: CHEBI:42645
+ S-fluorination
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a fluoro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an iodo group.
+ MOP:0004554
+ has_participant: CHEBI:43448
+ S-iodination
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an iodo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an imino group.
+ MOP:0004555
+ has_participant: CHEBI:29342
+ S-imination
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and an imino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nitro group.
+ MOP:0004556
+ has_participant: CHEBI:29785
+ S-nitration
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a nitro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a hydroxyamino group.
+ MOP:0004557
+ has_participant: CHEBI:29769
+ S-hydroxyamination
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a hydroxyamino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a thioxo group.
+ MOP:0004558
+ has_participant: CHEBI:29833
+ S-thioxonation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a thioxo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfo group.
+ MOP:0004559
+ has_participant: CHEBI:29922
+ S-sulfonation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a sulfo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a selenono group.
+ MOP:0004560
+ has_participant: CHEBI:29923
+ S-selenonation
+
+
+
+
+ Formation of a covalent bond between a sulfur atom in a substrate and a selenono group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a boryl group (-BR'R').
+ MOP:0005000
+ Submitted to ChEBI
+ C-borylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a boryl group (-BR'R').
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a methanidyl group.
+ MOP:0005001
+ has_participant: CHEBI:29361
+ C-methanidylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a methanidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an azaniumyl group.
+ MOP:0005002
+ has_participant: CHEBI:48284
+ C-azaniumylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an azaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a formyl group.
+ MOP:0005003
+ has_participant: CHEBI:42485
+ C-formylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a formyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acetonyl group.
+ MOP:0005004
+ has_participant: CHEBI:48056
+ C-acetonylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acetonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-cystyl group.
+ MOP:0005005
+ has_participant: CHEBI:50057
+ C-L-cystylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-cystinyl group.
+ MOP:0005006
+ has_participant: CHEBI:50066
+ C-L-cystinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-cystinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-cystyl group.
+ MOP:0005007
+ has_participant: CHEBI:50049
+ C-D-cystylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cystinyl group.
+ MOP:0005008
+ has_participant: CHEBI:50050
+ C-cystinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cystinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cystyl group.
+ MOP:0005009
+ has_participant: CHEBI:23514
+ C-cystylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cysteinyl group.
+ MOP:0005010
+ has_participant: CHEBI:23511
+ C-cysteinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-cysteinyl group.
+ MOP:0005011
+ has_participant: CHEBI:32447
+ C-L-cysteinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-cysteinyl group.
+ MOP:0005012
+ has_participant: CHEBI:32452
+ C-D-cysteinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-cysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cystein-S-yl group.
+ MOP:0005013
+ has_participant: CHEBI:32795
+ C-cystein-S-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-cystein-S-yl group.
+ MOP:0005014
+ has_participant: CHEBI:32794
+ C-D-cystein-S-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-cystein-S-yl group.
+ MOP:0005015
+ has_participant: CHEBI:32793
+ C-L-cystein-S-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-cystein-S-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a methionyl group.
+ MOP:0005016
+ has_participant: CHEBI:37902
+ C-methionylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-methionyl group.
+ MOP:0005017
+ has_participant: CHEBI:49038
+ C-L-methionylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-formyl-L-methionyl group.
+ MOP:0005018
+ has_participant: CHEBI:49298
+ C-N-formyl-L-methionylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-formyl-L-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-methionyl group.
+ MOP:0005019
+ has_participant: CHEBI:32640
+ C-D-methionylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-methionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an (R)-lipoyl group.
+ MOP:0005020
+ has_participant: CHEBI:38232
+ C-(R)-lipoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an (R)-lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an (S)-lipoyl group.
+ MOP:0005021
+ has_participant: CHEBI:38233
+ C-(S)-lipoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an (S)-lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a lipoyl group.
+ MOP:0005022
+ has_participant: CHEBI:25064
+ C-lipoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a lipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an (R)-dihydrolipoyl group.
+ MOP:0005023
+ has_participant: CHEBI:30319
+ C-(R)-dihydrolipoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an (R)-dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an (S)-dihydrolipoyl group.
+ MOP:0005024
+ has_participant: CHEBI:50489
+ C-(S)-dihydrolipoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an (S)-dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-sialoyl group.
+ MOP:0005025
+ has_participant: CHEBI:32960
+ C-alpha-sialoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-sialoyl group.
+ MOP:0005026
+ has_participant: CHEBI:32961
+ C-beta-sialoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glyceroyl group.
+ MOP:0005027
+ has_participant: CHEBI:30750
+ C-glyceroylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glyceroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carboacyl group.
+ MOP:0005028
+ has_participant: CHEBI:37838
+ C-carboacylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an univalent carboacyl group.
+ MOP:0005029
+ has_participant: CHEBI:27207
+ C-univalent carboacylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an univalent carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acetyl group.
+ MOP:0005030
+ has_participant: CHEBI:40574
+ C-acetylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-aminoacyl group.
+ MOP:0005031
+ has_participant: CHEBI:22487
+ C-alpha-aminoacylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-aminoacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alanyl group.
+ MOP:0005032
+ has_participant: CHEBI:22280
+ C-alanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-alanyl group.
+ MOP:0005033
+ has_participant: CHEBI:32433
+ C-L-alanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-alanyl group.
+ MOP:0005034
+ has_participant: CHEBI:32437
+ C-D-alanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-alanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-aspartyl group.
+ MOP:0005035
+ has_participant: CHEBI:22445
+ C-alpha-aspartylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-alpha-aspartyl group.
+ MOP:0005036
+ has_participant: CHEBI:32462
+ C-L-alpha-aspartylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-alpha-aspartyl group.
+ MOP:0005037
+ has_participant: CHEBI:32466
+ C-D-alpha-aspartylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-alpha-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-glutamyl group.
+ MOP:0005038
+ has_participant: CHEBI:22453
+ C-alpha-glutamylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-alpha-glutamyl group.
+ MOP:0005039
+ has_participant: CHEBI:46855
+ C-L-alpha-glutamylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-alpha-glutamyl group.
+ MOP:0005040
+ has_participant: CHEBI:32479
+ C-D-alpha-glutamylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-alpha-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pteroylglutamyl group.
+ MOP:0005041
+ has_participant: CHEBI:26380
+ C-pteroylglutamylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pteroylglutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phenylalanyl group.
+ MOP:0005042
+ has_participant: CHEBI:25987
+ C-phenylalanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-phenylalanyl group.
+ MOP:0005043
+ has_participant: CHEBI:32496
+ C-L-phenylalanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-phenylalanyl group.
+ MOP:0005044
+ has_participant: CHEBI:32500
+ C-D-phenylalanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-phenylalanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glycyl group.
+ MOP:0005045
+ has_participant: CHEBI:46740
+ C-glycylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glycyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a histidyl group.
+ MOP:0005046
+ has_participant: CHEBI:37906
+ C-histidylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-histidyl group.
+ MOP:0005047
+ has_participant: CHEBI:32514
+ C-L-histidylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-histidyl group.
+ MOP:0005048
+ has_participant: CHEBI:32522
+ C-D-histidylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-histidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an isoleucyl group.
+ MOP:0005049
+ has_participant: CHEBI:37905
+ C-isoleucylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-isoleucyl group.
+ MOP:0005050
+ has_participant: CHEBI:32606
+ C-L-isoleucylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-isoleucyl group.
+ MOP:0005051
+ has_participant: CHEBI:32610
+ C-D-isoleucylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-isoleucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a lysyl group.
+ MOP:0005052
+ has_participant: CHEBI:37903
+ C-lysylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-lysyl group.
+ MOP:0005053
+ has_participant: CHEBI:32553
+ C-L-lysylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a deoxyhypusinyl group.
+ MOP:0005054
+ has_participant: CHEBI:50039
+ C-deoxyhypusinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a deoxyhypusinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-lysyl group.
+ MOP:0005055
+ has_participant: CHEBI:32559
+ C-D-lysylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-lysyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a leucyl group.
+ MOP:0005056
+ has_participant: CHEBI:37904
+ C-leucylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-leucyl group.
+ MOP:0005057
+ has_participant: CHEBI:32621
+ C-L-leucylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-leucyl group.
+ MOP:0005058
+ has_participant: CHEBI:32625
+ C-D-leucylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-leucyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an asparaginyl group.
+ MOP:0005059
+ has_participant: CHEBI:22656
+ C-asparaginylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-asparaginyl group.
+ MOP:0005060
+ has_participant: CHEBI:50348
+ C-L-asparaginylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-asparaginyl group.
+ MOP:0005061
+ has_participant: CHEBI:32653
+ C-D-asparaginylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-asparaginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a prolyl group.
+ MOP:0005062
+ has_participant: CHEBI:26274
+ C-prolylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-prolyl group.
+ MOP:0005063
+ has_participant: CHEBI:32865
+ C-L-prolylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-prolyl group.
+ MOP:0005064
+ has_participant: CHEBI:32869
+ C-D-prolylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-prolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glutaminyl group.
+ MOP:0005065
+ has_participant: CHEBI:24320
+ C-glutaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-glutaminyl group.
+ MOP:0005066
+ has_participant: CHEBI:32667
+ C-L-glutaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-glutaminyl group.
+ MOP:0005067
+ has_participant: CHEBI:32674
+ C-D-glutaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-glutaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a seryl group.
+ MOP:0005068
+ has_participant: CHEBI:37901
+ C-serylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-seryl group.
+ MOP:0005069
+ has_participant: CHEBI:32838
+ C-L-serylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-seryl group.
+ MOP:0005070
+ has_participant: CHEBI:32842
+ C-D-serylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-seryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a threonyl group.
+ MOP:0005071
+ has_participant: CHEBI:37900
+ C-threonylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-threonyl group.
+ MOP:0005072
+ has_participant: CHEBI:32823
+ C-L-threonylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-threonyl group.
+ MOP:0005073
+ has_participant: CHEBI:32829
+ C-D-threonylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-threonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a selenocysteinyl group.
+ MOP:0005074
+ has_participant: CHEBI:32755
+ C-selenocysteinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-selenocysteinyl group.
+ MOP:0005075
+ has_participant: CHEBI:32745
+ C-L-selenocysteinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-selenocysteinyl group.
+ MOP:0005076
+ has_participant: CHEBI:32749
+ C-D-selenocysteinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-selenocysteinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a valyl group.
+ MOP:0005077
+ has_participant: CHEBI:37897
+ C-valylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-valyl group.
+ MOP:0005078
+ has_participant: CHEBI:32853
+ C-L-valylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-valyl group.
+ MOP:0005079
+ has_participant: CHEBI:32857
+ C-D-valylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-valyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tryptophyl group.
+ MOP:0005080
+ has_participant: CHEBI:37899
+ C-tryptophylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-tryptophyl group.
+ MOP:0005081
+ has_participant: CHEBI:32706
+ C-L-tryptophylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-tryptophyl group.
+ MOP:0005082
+ has_participant: CHEBI:32718
+ C-D-tryptophylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-tryptophyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tyrosyl group.
+ MOP:0005083
+ has_participant: CHEBI:37898
+ C-tyrosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-tyrosyl group.
+ MOP:0005084
+ has_participant: CHEBI:32764
+ C-L-tyrosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-tyrosyl group.
+ MOP:0005085
+ has_participant: CHEBI:32778
+ C-D-tyrosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-tyrosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arginyl group.
+ MOP:0005086
+ has_participant: CHEBI:22619
+ C-arginylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-arginyl group.
+ MOP:0005087
+ has_participant: CHEBI:32684
+ C-L-arginylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-arginyl group.
+ MOP:0005088
+ has_participant: CHEBI:32691
+ C-D-arginylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-arginyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a benzoyl group.
+ MOP:0005089
+ has_participant: CHEBI:22733
+ C-benzoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a benzoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-aspartyl group.
+ MOP:0005090
+ has_participant: CHEBI:22832
+ C-beta-aspartylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-beta-aspartyl group.
+ MOP:0005091
+ has_participant: CHEBI:32467
+ C-D-beta-aspartylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-beta-aspartyl group.
+ MOP:0005092
+ has_participant: CHEBI:48098
+ C-L-beta-aspartylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-beta-aspartyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a biotinyl group.
+ MOP:0005093
+ has_participant: CHEBI:22885
+ C-biotinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a biotinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a butyryl group.
+ MOP:0005094
+ has_participant: CHEBI:22972
+ C-butyrylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a butyryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carbamoyl group.
+ MOP:0005095
+ has_participant: CHEBI:23004
+ C-carbamoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carbamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a C-aminocarbonohydrazonoyl group.
+ MOP:0005096
+ has_participant: CHEBI:48223
+ C-C-aminocarbonohydrazonoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a C-aminocarbonohydrazonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-(aminomethylidene)hydrazinyl group.
+ MOP:0005097
+ has_participant: CHEBI:48244
+ C-2-(aminomethylidene)hydrazinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-(aminomethylidene)hydrazinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carbamoylcarbamoyl group.
+ MOP:0005098
+ has_participant: CHEBI:48083
+ C-carbamoylcarbamoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carbamoylcarbamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carbamothioyl group.
+ MOP:0005099
+ has_participant: CHEBI:48225
+ C-carbamothioylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carbamothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acetylazanediyl group.
+ MOP:0005100
+ has_participant: CHEBI:48073
+ C-acetylazanediylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acetylazanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an oxamoyl group.
+ MOP:0005101
+ has_participant: CHEBI:48246
+ C-oxamoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an oxamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cholyl group.
+ MOP:0005102
+ has_participant: CHEBI:23220
+ C-cholylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cholyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an enoyl group.
+ MOP:0005103
+ has_participant: CHEBI:23916
+ C-enoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a fatty-acyl group.
+ MOP:0005104
+ has_participant: CHEBI:24027
+ C-fatty-acylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a fatty-acyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arachidonoyl group.
+ MOP:0005105
+ has_participant: CHEBI:22610
+ C-arachidonoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arachidonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arachidoyl group.
+ MOP:0005106
+ has_participant: CHEBI:22614
+ C-arachidoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arachidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a behenoyl group.
+ MOP:0005107
+ has_participant: CHEBI:22696
+ C-behenoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a behenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cerotoyl group.
+ MOP:0005108
+ has_participant: CHEBI:23080
+ C-cerotoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cerotoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a decanoyl group.
+ MOP:0005109
+ has_participant: CHEBI:23574
+ C-decanoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a decanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a dodecenoyl group.
+ MOP:0005110
+ has_participant: CHEBI:23868
+ C-dodecenoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a dodecenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an eleostearoyl group.
+ MOP:0005111
+ has_participant: CHEBI:23908
+ C-eleostearoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an eleostearoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a mycolyl group.
+ MOP:0005112
+ has_participant: CHEBI:25439
+ C-mycolylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a mycolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nervonoyl group.
+ MOP:0005113
+ has_participant: CHEBI:25503
+ C-nervonoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nervonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an octanoyl group.
+ MOP:0005114
+ has_participant: CHEBI:25650
+ C-octanoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an octanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a palmitoleoyl group.
+ MOP:0005115
+ has_participant: CHEBI:25837
+ C-palmitoleoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a palmitoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a palmitoyl group.
+ MOP:0005116
+ has_participant: CHEBI:45021
+ C-palmitoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a palmitoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a stearoyl group.
+ MOP:0005117
+ has_participant: CHEBI:26753
+ C-stearoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a stearoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an undecanoyl group.
+ MOP:0005118
+ has_participant: CHEBI:27190
+ C-undecanoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an undecanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a valeryl group.
+ MOP:0005119
+ has_participant: CHEBI:27265
+ C-valerylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a valeryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a hexanoyl group.
+ MOP:0005120
+ has_participant: CHEBI:24574
+ C-hexanoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a hexanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a heptanoyl group.
+ MOP:0005121
+ has_participant: CHEBI:32363
+ C-heptanoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a heptanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nonanoyl group.
+ MOP:0005122
+ has_participant: CHEBI:25580
+ C-nonanoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nonanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a lauroyl group.
+ MOP:0005123
+ has_participant: CHEBI:32359
+ C-lauroylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a lauroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a myristoyl group.
+ MOP:0005124
+ has_participant: CHEBI:25456
+ C-myristoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a myristoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a docosenoyl group.
+ MOP:0005125
+ has_participant: CHEBI:50479
+ C-docosenoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a docosenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cetoleoyl group.
+ MOP:0005126
+ has_participant: CHEBI:32430
+ C-cetoleoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cetoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an erucoyl group.
+ MOP:0005127
+ has_participant: CHEBI:32394
+ C-erucoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an erucoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an icosenoyl group.
+ MOP:0005128
+ has_participant: CHEBI:50480
+ C-icosenoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an icosenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a gadelaidoyl group.
+ MOP:0005129
+ has_participant: CHEBI:32424
+ C-gadelaidoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a gadelaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a gadoleoyl group.
+ MOP:0005130
+ has_participant: CHEBI:32421
+ C-gadoleoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a gadoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a gondoyl group.
+ MOP:0005131
+ has_participant: CHEBI:32427
+ C-gondoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a gondoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a heptatrienoyl group.
+ MOP:0005132
+ has_participant: CHEBI:50486
+ C-heptatrienoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a heptatrienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trans,trans-hepta-2,4,6-trienoyl group.
+ MOP:0005133
+ has_participant: CHEBI:30771
+ C-trans,trans-hepta-2,4,6-trienoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trans,trans-hepta-2,4,6-trienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an octadecenoyl group.
+ MOP:0005134
+ has_participant: CHEBI:50499
+ C-octadecenoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an octadecenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an octadec-6-enoyl group.
+ MOP:0005135
+ has_participant: CHEBI:50497
+ C-octadec-6-enoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an octadec-6-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a petroselaidoyl group.
+ MOP:0005136
+ has_participant: CHEBI:32378
+ C-petroselaidoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a petroselaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a petroselinoyl group.
+ MOP:0005137
+ has_participant: CHEBI:32376
+ C-petroselinoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a petroselinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a vaccenoyl group.
+ MOP:0005138
+ has_participant: CHEBI:27261
+ C-vaccenoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cis-vaccenoyl group.
+ MOP:0005139
+ has_participant: CHEBI:23313
+ C-cis-vaccenoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cis-vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trans-vaccenoyl group.
+ MOP:0005140
+ has_participant: CHEBI:27080
+ C-trans-vaccenoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trans-vaccenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an octadec-9-enoyl group.
+ MOP:0005141
+ has_participant: CHEBI:50500
+ C-octadec-9-enoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an octadec-9-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an oleoyl group.
+ MOP:0005142
+ has_participant: CHEBI:25667
+ C-oleoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an oleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an elaidoyl group.
+ MOP:0005143
+ has_participant: CHEBI:23904
+ C-elaidoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an elaidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a margaroyl group.
+ MOP:0005144
+ has_participant: CHEBI:32367
+ C-margaroylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a margaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a melissoyl group.
+ MOP:0005145
+ has_participant: CHEBI:31016
+ C-melissoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a melissoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a myristoleoyl group.
+ MOP:0005146
+ has_participant: CHEBI:32371
+ C-myristoleoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a myristoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an obtusiloyl group.
+ MOP:0005147
+ has_participant: CHEBI:33162
+ C-obtusiloylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an obtusiloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a lignoceroyl group.
+ MOP:0005148
+ has_participant: CHEBI:31015
+ C-lignoceroylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a lignoceroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a linoleoyl group.
+ MOP:0005149
+ has_participant: CHEBI:32386
+ C-linoleoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a linoleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a parinaroyl group.
+ MOP:0005150
+ has_participant: CHEBI:50501
+ C-parinaroylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cis-parinaroyl group.
+ MOP:0005151
+ has_participant: CHEBI:32415
+ C-cis-parinaroylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cis-parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trans-parinaroyl group.
+ MOP:0005152
+ has_participant: CHEBI:32417
+ C-trans-parinaroylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trans-parinaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a gamma-glutamyl group.
+ MOP:0005153
+ has_participant: CHEBI:24190
+ C-gamma-glutamylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-gamma-glutamyl group.
+ MOP:0005154
+ has_participant: CHEBI:32474
+ C-L-gamma-glutamylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-gamma-glutamyl group.
+ MOP:0005155
+ has_participant: CHEBI:32480
+ C-D-gamma-glutamylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-gamma-glutamyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glucuronosyl group.
+ MOP:0005156
+ has_participant: CHEBI:24303
+ C-glucuronosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glucuronosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-glucuronoyl group.
+ MOP:0005157
+ has_participant: CHEBI:24307
+ C-D-glucuronoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-glucuronoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glyceroyl 2,3-dihydroxypropanoyl group.
+ MOP:0005158
+ has_participant: CHEBI:24363
+ C-glyceroyl 2,3-dihydroxypropanoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glyceroyl 2,3-dihydroxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glyceryl group.
+ MOP:0005159
+ has_participant: CHEBI:24364
+ C-glycerylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glyceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glycidoyl 2,3-epoxypropanoyl group.
+ MOP:0005160
+ has_participant: CHEBI:24365
+ C-glycidoyl 2,3-epoxypropanoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glycidoyl 2,3-epoxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glycoloyl group.
+ MOP:0005161
+ has_participant: CHEBI:30884
+ C-glycoloylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glycoloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glycosyl group.
+ MOP:0005162
+ has_participant: CHEBI:24403
+ C-glycosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glycosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a galactosyl group.
+ MOP:0005163
+ has_participant: CHEBI:24164
+ C-galactosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-D-galactosyl group.
+ MOP:0005168
+ MOP:0005164
+ has_participant: CHEBI:22778
+ C-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-L-fucosyl-1,2-beta-D-galactosyl group.
+ MOP:0005165
+ has_participant: CHEBI:16124
+ C-alpha-L-fucosyl-1,2-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-L-fucosyl-1,2-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ MOP:0005166
+ has_participant: CHEBI:16361
+ C-alpha-N-acetylneuraminyl-2,3-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ MOP:0005167
+ has_participant: CHEBI:17483
+ C-alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-N-acetylneuraminyl-2,8-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glucosyl group.
+ MOP:0005172
+ MOP:0005169
+ has_participant: CHEBI:24281
+ C-glucosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosyl group.
+ MOP:0005170
+ has_participant: CHEBI:17227
+ C-D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-galactosyl-1,3-beta-D-galactosyl-1,4-beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-galactosyl-1,4beta-D-glucosyl group.
+ MOP:0005171
+ has_participant: CHEBI:20966
+ C-D-galactosyl-1,4beta-D-glucosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-galactosyl-1,4beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-glucosyl group.
+ MOP:0005173
+ has_participant: CHEBI:30684
+ C-alpha-glucosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-glucosyl group.
+ MOP:0005174
+ has_participant: CHEBI:30697
+ C-beta-glucosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-galactosyl-(1->4)-beta-D-glucosyl group.
+ MOP:0005175
+ has_participant: CHEBI:18018
+ C-D-galactosyl-(1->4)-beta-D-glucosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-galactosyl-(1->4)-beta-D-glucosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glycosaminyl group.
+ MOP:0005176
+ has_participant: CHEBI:24399
+ C-glycosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glycosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a galactosaminyl group.
+ MOP:0005177
+ has_participant: CHEBI:24160
+ C-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-D-galactosaminyl group.
+ MOP:0005178
+ has_participant: CHEBI:21507
+ C-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0005179
+ has_participant: CHEBI:17850
+ C-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-(alpha-N-acetylneuraminyl-2,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ MOP:0005180
+ has_participant: CHEBI:16565
+ C-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ MOP:0005181
+ has_participant: CHEBI:16901
+ C-alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0005182
+ has_participant: CHEBI:15876
+ C-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0005183
+ has_participant: CHEBI:17723
+ C-beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-D-galactosyl-1,3-(N-acetyl-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ MOP:0005184
+ has_participant: CHEBI:16117
+ C-beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-D-galactosyl-1,3-N-acetyl-alpha-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ MOP:0005185
+ has_participant: CHEBI:22783
+ C-beta-D-galactosyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-D-galactosyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ MOP:0005186
+ has_participant: CHEBI:17581
+ C-N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,6)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminyl group.
+ MOP:0005187
+ has_participant: CHEBI:16250
+ C-N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminyl group.
+ MOP:0005188
+ has_participant: CHEBI:16478
+ C-N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,3)-N-acetyl-D-galactosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glucosaminyl group.
+ MOP:0005189
+ has_participant: CHEBI:24272
+ C-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-D-glucosaminyl group.
+ MOP:0005190
+ has_participant: CHEBI:21524
+ C-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ MOP:0005191
+ has_participant: CHEBI:18914
+ C-1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 1,3-beta-D-galactosyl-(1,4-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 3-O-beta-D-galactosyl-N-acetyl-D-glucosaminyl group.
+ MOP:0005192
+ has_participant: CHEBI:18915
+ C-3-O-beta-D-galactosyl-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 3-O-beta-D-galactosyl-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ MOP:0005193
+ has_participant: CHEBI:18939
+ C-1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 1,4-beta-D-galactosyl-(1,3-alpha-L-fucosyl)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0005194
+ has_participant: CHEBI:17571
+ C-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0005195
+ has_participant: CHEBI:17785
+ C-alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-D-galactosyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0005196
+ has_participant: CHEBI:22381
+ C-alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-D-galactosyl-beta-1,3-D-galactosyl-beta-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminyl group.
+ MOP:0005197
+ has_participant: CHEBI:22779
+ C-beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-D-galactosyl-(1,4)-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0005198
+ has_participant: CHEBI:21580
+ C-N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-(N-acetyl-beta-D-glucosaminyl-1,6)-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0005199
+ has_participant: CHEBI:21581
+ C-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3(6)-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl,1,6(3))-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0005200
+ has_participant: CHEBI:21582
+ C-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-(N-acetyl-beta-D-glucosaminyl-1,4)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ MOP:0005201
+ has_participant: CHEBI:21583
+ C-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl-1,4-N-acetyl-beta-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0005202
+ has_participant: CHEBI:16059
+ C-N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,3-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ MOP:0005203
+ has_participant: CHEBI:16198
+ C-N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-beta-D-galactosyl-1,4-N-acetyl-D-glucosaminyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an iduronosyl group.
+ MOP:0005204
+ has_participant: CHEBI:24770
+ C-iduronosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an iduronosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-inosinyl group.
+ MOP:0005205
+ has_participant: CHEBI:24845
+ C-5'-inosinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-inosinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a mannosyl group.
+ MOP:0005209
+ MOP:0005206
+ has_participant: CHEBI:25171
+ C-mannosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a (N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ MOP:0005207
+ has_participant: CHEBI:18638
+ C-(N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a (N-acetyl-beta-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-D-mannosyl-1,3-(r1)-beta-D-mannosyl group.
+ MOP:0005208
+ has_participant: CHEBI:22406
+ C-alpha-D-mannosyl-1,3-(r1)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-D-mannosyl-1,3-(r1)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-mannosyl group.
+ MOP:0005210
+ has_participant: CHEBI:30689
+ C-alpha-mannosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosyl group.
+ MOP:0005211
+ has_participant: CHEBI:32618
+ C-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosyl group.
+ MOP:0005212
+ has_participant: CHEBI:32890
+ C-N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2-alpha-D-mannosyl-1,3)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ MOP:0005213
+ has_participant: CHEBI:21589
+ C-N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,4-(N-acetyl-D-glucosaminyl-1,2)-alpha-D-mannosyl-1,3-(beta-N-acetyl-D-glucosaminyl-1,2-alpha-D-mannosyl-1,6)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosyl group.
+ MOP:0005214
+ has_participant: CHEBI:32601
+ C-N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosyl group.
+ MOP:0005215
+ has_participant: CHEBI:32602
+ C-N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-acetyl-beta-D-glucosaminyl-1,6-(N-acetyl-beta-D-glucosaminyl-1,2)-(N-acetyl-beta-D-glucosaminyl-1,4)-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-D-mannosyl-(1->3)-beta-D-mannosyl group.
+ MOP:0005216
+ has_participant: CHEBI:32591
+ C-alpha-D-mannosyl-(1->3)-beta-D-mannosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-D-mannosyl-(1->3)-beta-D-mannosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a neuraminosyl group.
+ MOP:0005217
+ has_participant: CHEBI:25509
+ C-neuraminosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a neuraminosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a neuraminoyl group.
+ MOP:0005218
+ has_participant: CHEBI:25510
+ C-neuraminoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a neuraminoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a ribosyl group.
+ MOP:0005221
+ MOP:0005219
+ has_participant: CHEBI:26566
+ C-ribosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a ribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an adenosinediphosphoribosyl group.
+ MOP:0005220
+ has_participant: CHEBI:22259
+ C-adenosinediphosphoribosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an adenosinediphosphoribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-deoxyribosyl group.
+ MOP:0005222
+ has_participant: CHEBI:30720
+ C-2-deoxyribosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-deoxyribosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sialosyl group.
+ MOP:0005223
+ has_participant: CHEBI:26668
+ C-sialosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sialosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a hemicystyl group.
+ MOP:0005224
+ has_participant: CHEBI:24492
+ C-hemicystylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a hemicystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a mevalonoyl group.
+ MOP:0005225
+ has_participant: CHEBI:25353
+ C-mevalonoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a mevalonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a montanoyl group.
+ MOP:0005226
+ has_participant: CHEBI:25417
+ C-montanoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a montanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a muramyl group.
+ MOP:0005227
+ has_participant: CHEBI:25433
+ C-muramylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nucleotidyl group.
+ MOP:0005228
+ has_participant: CHEBI:25613
+ C-nucleotidylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nucleotidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-adenylyl group.
+ MOP:0005229
+ has_participant: CHEBI:22263
+ C-5'-adenylylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-adenylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-cytidylyl group.
+ MOP:0005230
+ has_participant: CHEBI:23526
+ C-5'-cytidylylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-cytidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-thymidylyl group.
+ MOP:0005231
+ has_participant: CHEBI:27003
+ C-5'-thymidylylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-thymidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-uridylyl group.
+ MOP:0005232
+ has_participant: CHEBI:27244
+ C-5'-uridylylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-uridylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-guanylyl group.
+ MOP:0005233
+ has_participant: CHEBI:24460
+ C-5'-guanylylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-guanylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-ribothymidylyl group.
+ MOP:0005234
+ has_participant: CHEBI:26569
+ C-5'-ribothymidylylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-ribothymidylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-inosinylyl group.
+ MOP:0005235
+ has_participant: CHEBI:33512
+ C-5'-inosinylylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-inosinylyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pantothenyl group.
+ MOP:0005236
+ has_participant: CHEBI:25850
+ C-pantothenylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pantothenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pantoyl group.
+ MOP:0005237
+ has_participant: CHEBI:25851
+ C-pantoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pantoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a peptidyl group.
+ MOP:0005238
+ has_participant: CHEBI:25907
+ C-peptidylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a peptidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phthalyl group.
+ MOP:0005239
+ has_participant: CHEBI:26096
+ C-phthalylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phthalyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a propionyl group.
+ MOP:0005240
+ has_participant: CHEBI:26294
+ C-propionylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a propionyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pyruvoyl group.
+ MOP:0005241
+ has_participant: CHEBI:45360
+ C-pyruvoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pyruvoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a retinoyl group.
+ MOP:0005242
+ has_participant: CHEBI:26539
+ C-retinoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a retinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sialoyl group.
+ MOP:0005243
+ has_participant: CHEBI:26670
+ C-sialoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sialoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 3-carboxypropanoyl group.
+ MOP:0005244
+ has_participant: CHEBI:26810
+ C-3-carboxypropanoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 3-carboxypropanoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trienoyl group.
+ MOP:0005245
+ has_participant: CHEBI:27107
+ C-trienoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trienoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an anilinocarbonyl group.
+ MOP:0005246
+ has_participant: CHEBI:30692
+ C-anilinocarbonylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an anilinocarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pteroyl group.
+ MOP:0005247
+ has_participant: CHEBI:26379
+ C-pteroylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pteroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 3-carboxyprop-2-enoyl group.
+ MOP:0005248
+ has_participant: CHEBI:37953
+ C-3-carboxyprop-2-enoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a (Z)-3-carboxyprop-2-enoyl group.
+ MOP:0005249
+ has_participant: CHEBI:25122
+ C-(Z)-3-carboxyprop-2-enoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a (Z)-3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a (E)-3-carboxyprop-2-enoyl group.
+ MOP:0005250
+ has_participant: CHEBI:24126
+ C-(E)-3-carboxyprop-2-enoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a (E)-3-carboxyprop-2-enoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2,6-dichlorobenzoyl group.
+ MOP:0005251
+ has_participant: CHEBI:48625
+ C-2,6-dichlorobenzoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2,6-dichlorobenzoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-muramyl group.
+ MOP:0005252
+ has_participant: CHEBI:30701
+ C-alpha-muramylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-muramyl group.
+ MOP:0005253
+ has_participant: CHEBI:30702
+ C-beta-muramylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a beta-muramyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a dihydrolipoyl group.
+ MOP:0005254
+ has_participant: CHEBI:50488
+ C-dihydrolipoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a dihydrolipoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sinapoyl group.
+ MOP:0005255
+ has_participant: CHEBI:50561
+ C-sinapoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sinapoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carboxyacetyl group.
+ MOP:0005256
+ has_participant: CHEBI:50650
+ C-carboxyacetylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carboxyacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a divalent carboacyl group.
+ MOP:0005257
+ has_participant: CHEBI:23855
+ C-divalent carboacylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a divalent carboacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an aspartoyl group.
+ MOP:0005258
+ has_participant: CHEBI:22663
+ C-aspartoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-aspartoyl group.
+ MOP:0005259
+ has_participant: CHEBI:32464
+ C-L-aspartoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-aspartoyl group.
+ MOP:0005260
+ has_participant: CHEBI:32468
+ C-D-aspartoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-aspartoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a citraconoyl group.
+ MOP:0005261
+ has_participant: CHEBI:23315
+ C-citraconoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a citraconoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glutamoyl group.
+ MOP:0005262
+ has_participant: CHEBI:24322
+ C-glutamoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-glutamoyl group.
+ MOP:0005263
+ has_participant: CHEBI:32481
+ C-D-glutamoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-glutamoyl group.
+ MOP:0005264
+ has_participant: CHEBI:32475
+ C-L-glutamoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-glutamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a maloyl group.
+ MOP:0005265
+ has_participant: CHEBI:25138
+ C-maloylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a maloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phthaloyl group.
+ MOP:0005266
+ has_participant: CHEBI:26095
+ C-phthaloylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phthaloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a succinyl group.
+ MOP:0005267
+ has_participant: CHEBI:37952
+ C-succinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a succinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a butenedioyl group.
+ MOP:0005268
+ has_participant: CHEBI:37954
+ C-butenedioylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a butenedioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a fumaroyl group.
+ MOP:0005269
+ has_participant: CHEBI:24125
+ C-fumaroylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a fumaroyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a maleoyl group.
+ MOP:0005270
+ has_participant: CHEBI:25121
+ C-maleoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a maleoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a hexanedioyl group.
+ MOP:0005271
+ has_participant: CHEBI:48082
+ C-hexanedioylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a hexanedioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a malonyl group.
+ MOP:0005272
+ has_participant: CHEBI:25134
+ C-malonylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a malonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an ornithyl group.
+ MOP:0005273
+ has_participant: CHEBI:46929
+ C-ornithylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an ornithyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-ornithyl group.
+ MOP:0005274
+ has_participant: CHEBI:44700
+ C-L-ornithylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-ornithyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a half-cystyl group.
+ MOP:0005275
+ has_participant: CHEBI:30770
+ C-half-cystylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a half-cystyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-tyrosin-O(4)-yl group.
+ MOP:0005276
+ has_participant: CHEBI:32768
+ C-L-tyrosin-O(4)-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-threonin-O(3)-yl group.
+ MOP:0005277
+ has_participant: CHEBI:32825
+ C-L-threonin-O(3)-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an L-threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-tyrosin-O(4)-yl group.
+ MOP:0005278
+ has_participant: CHEBI:32780
+ C-D-tyrosin-O(4)-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-threonin-O(3)-yl group.
+ MOP:0005279
+ has_participant: CHEBI:32831
+ C-D-threonin-O(3)-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a D-threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tyrosin-O(4)-yl group.
+ MOP:0005280
+ has_participant: CHEBI:32788
+ C-tyrosin-O(4)-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tyrosin-O(4)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a threonin-O(3)-yl group.
+ MOP:0005281
+ has_participant: CHEBI:26985
+ C-threonin-O(3)-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a threonin-O(3)-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an oxalyl group.
+ MOP:0005282
+ has_participant: CHEBI:30870
+ C-oxalylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an oxalyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a fumagillin-2-yl group.
+ MOP:0005283
+ has_participant: CHEBI:42601
+ C-fumagillin-2-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a fumagillin-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acetoacetyl group.
+ MOP:0005284
+ has_participant: CHEBI:48051
+ C-acetoacetylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acetoacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-linolenoyl group.
+ MOP:0005285
+ has_participant: CHEBI:32388
+ C-alpha-linolenoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alpha-linolenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a gamma-linolenoyl group.
+ MOP:0005286
+ has_participant: CHEBI:32390
+ C-gamma-linolenoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a gamma-linolenoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carbamimidoyl group.
+ MOP:0005287
+ has_participant: CHEBI:48090
+ C-carbamimidoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carbamimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a formimidoyl group.
+ MOP:0005288
+ has_participant: CHEBI:24084
+ C-formimidoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a formimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trifluoroacetyl group.
+ MOP:0005289
+ has_participant: CHEBI:45888
+ C-trifluoroacetylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trifluoroacetyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carboxymethyl group.
+ MOP:0005290
+ has_participant: CHEBI:41402
+ C-carboxymethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carboxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a methylenecarbonyl group.
+ MOP:0005291
+ has_participant: CHEBI:43923
+ C-methylenecarbonylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a methylenecarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-hydroxyacetimidoyl group.
+ MOP:0005292
+ has_participant: CHEBI:48055
+ C-N-hydroxyacetimidoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-hydroxyacetimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acryloyl group.
+ MOP:0005293
+ has_participant: CHEBI:48077
+ C-acryloylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acryloyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tert-butoxycarbonyl group.
+ MOP:0005294
+ has_participant: CHEBI:48502
+ C-tert-butoxycarbonylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tert-butoxycarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfanediyl group.
+ MOP:0005295
+ has_participant: CHEBI:29830
+ C-sulfanediylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phenylsulfanyl group.
+ MOP:0005296
+ has_participant: CHEBI:48499
+ C-phenylsulfanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phenylsulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a methylsulfanyl group.
+ MOP:0005297
+ has_participant: CHEBI:48563
+ C-methylsulfanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a methylsulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfaniumyl group.
+ MOP:0005298
+ has_participant: CHEBI:36945
+ C-sulfaniumylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a disulfanidyl group.
+ MOP:0005299
+ has_participant: CHEBI:29838
+ C-disulfanidylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a disulfanidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a disulfanediyl group.
+ MOP:0005300
+ has_participant: CHEBI:29826
+ C-disulfanediylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a disulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a disulfanyl group.
+ MOP:0005301
+ has_participant: CHEBI:30605
+ C-disulfanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a disulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tetrasulfanyl group.
+ MOP:0005302
+ has_participant: CHEBI:30607
+ C-tetrasulfanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tetrasulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tetrasulfanediyl group.
+ MOP:0005303
+ has_participant: CHEBI:29836
+ C-tetrasulfanediylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tetrasulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trisulfanyl group.
+ MOP:0005304
+ has_participant: CHEBI:30606
+ C-trisulfanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trisulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trisulfanediyl group.
+ MOP:0005305
+ has_participant: CHEBI:29834
+ C-trisulfanediylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trisulfanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pentasulfanyl group.
+ MOP:0005306
+ has_participant: CHEBI:30608
+ C-pentasulfanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pentasulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a diselanyl group.
+ MOP:0005307
+ has_participant: CHEBI:30602
+ C-diselanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a diselanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tellanyl group.
+ MOP:0005308
+ has_participant: CHEBI:30458
+ C-tellanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tellanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tellanediyl group.
+ MOP:0005309
+ has_participant: CHEBI:30455
+ C-tellanediylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tellanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tellaniumyl group.
+ MOP:0005310
+ has_participant: CHEBI:30447
+ C-tellaniumylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tellaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a ditellanyl group.
+ MOP:0005311
+ has_participant: CHEBI:30601
+ C-ditellanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a ditellanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an amidyl group.
+ MOP:0005312
+ has_participant: CHEBI:48373
+ C-amidylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an amidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an azanediyl group.
+ MOP:0005313
+ has_participant: CHEBI:29343
+ C-azanediylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an azanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-aminoethyl group.
+ MOP:0005314
+ has_participant: CHEBI:22502
+ C-2-aminoethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-aminoethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 4-aminobutyl group.
+ MOP:0005315
+ has_participant: CHEBI:50339
+ C-4-aminobutylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 4-aminobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an azanetriyl group.
+ MOP:0005316
+ has_participant: CHEBI:30228
+ C-azanetriylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an azanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a hydrazine-1,2-diyl group.
+ MOP:0005317
+ has_participant: CHEBI:30098
+ C-hydrazine-1,2-diylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a hydrazine-1,2-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a diazyn-1-ium-1-yl group.
+ MOP:0005318
+ has_participant: CHEBI:30108
+ C-diazyn-1-ium-1-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a diazyn-1-ium-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phosphanetriyl group.
+ MOP:0005319
+ has_participant: CHEBI:30206
+ C-phosphanetriylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phosphanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phosphanediyl group.
+ MOP:0005320
+ has_participant: CHEBI:29944
+ C-phosphanediylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phosphanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phosphanyl group.
+ MOP:0005321
+ has_participant: CHEBI:29936
+ C-phosphanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phosphanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a lambda(5)-phosphanyl group.
+ MOP:0005322
+ has_participant: CHEBI:30284
+ C-lambda(5)-phosphanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a lambda(5)-phosphanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phosphaniumyl group.
+ MOP:0005323
+ has_participant: CHEBI:30279
+ C-phosphaniumylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phosphaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arsanyl group.
+ MOP:0005324
+ has_participant: CHEBI:29759
+ C-arsanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arsanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arsanediyl group.
+ MOP:0005325
+ has_participant: CHEBI:29763
+ C-arsanediylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arsanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arsanetriyl group.
+ MOP:0005326
+ has_participant: CHEBI:29766
+ C-arsanetriylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arsanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arsaniumyl group.
+ MOP:0005327
+ has_participant: CHEBI:29842
+ C-arsaniumylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arsaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a lambda(5)-arsanyl group.
+ MOP:0005328
+ has_participant: CHEBI:30273
+ C-lambda(5)-arsanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a lambda(5)-arsanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a stibaniumyl group.
+ MOP:0005329
+ has_participant: CHEBI:30291
+ C-stibaniumylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a stibaniumyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a lambda(5)-stibanyl group.
+ MOP:0005330
+ has_participant: CHEBI:30293
+ C-lambda(5)-stibanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a lambda(5)-stibanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a boranyl group.
+ MOP:0005331
+ has_participant: CHEBI:33604
+ C-boranylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a boranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a boranetriyl group.
+ MOP:0005332
+ has_participant: CHEBI:30169
+ C-boranetriylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a boranetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a boranediyl group.
+ MOP:0005333
+ has_participant: CHEBI:38988
+ C-boranediylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a boranediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a boranuidyl group.
+ MOP:0005334
+ has_participant: CHEBI:30159
+ C-boranuidylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a boranuidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a germyl group.
+ MOP:0005335
+ has_participant: CHEBI:30542
+ C-germylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a germyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a germanediyl group.
+ MOP:0005336
+ has_participant: CHEBI:30554
+ C-germanediylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a germanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a germanetetrayl group.
+ MOP:0005337
+ has_participant: CHEBI:30547
+ C-germanetetraylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a germanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a germanetriyl group.
+ MOP:0005338
+ has_participant: CHEBI:30544
+ C-germanetriylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a germanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a silyl group.
+ MOP:0005339
+ has_participant: CHEBI:30541
+ C-silylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a silyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a silanediyl group.
+ MOP:0005340
+ has_participant: CHEBI:30587
+ C-silanediylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a silanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a silanetriyl group.
+ MOP:0005341
+ has_participant: CHEBI:30576
+ C-silanetriylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a silanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a silanetetrayl group.
+ MOP:0005342
+ has_participant: CHEBI:30583
+ C-silanetetraylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a silanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a disilanyl group.
+ MOP:0005343
+ has_participant: CHEBI:30594
+ C-disilanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a disilanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alumanyl group.
+ MOP:0005344
+ has_participant: CHEBI:30135
+ C-alumanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alumanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a stannyl group.
+ MOP:0005345
+ has_participant: CHEBI:30540
+ C-stannylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a stannyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a stannanetriyl group.
+ MOP:0005346
+ has_participant: CHEBI:30575
+ C-stannanetriylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a stannanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a plumbanetriyl group.
+ MOP:0005347
+ has_participant: CHEBI:30577
+ C-plumbanetriylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a plumbanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a plumbyl group.
+ MOP:0005348
+ has_participant: CHEBI:30543
+ C-plumbylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a plumbyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a gallanyl group.
+ MOP:0005349
+ has_participant: CHEBI:37119
+ C-gallanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a gallanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an indiganyl group.
+ MOP:0005350
+ has_participant: CHEBI:30431
+ C-indiganylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an indiganyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a thallanyl group.
+ MOP:0005351
+ has_participant: CHEBI:30442
+ C-thallanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a thallanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phosphatidyl group.
+ MOP:0005352
+ has_participant: CHEBI:26025
+ C-phosphatidylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phosphatidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nucleosidyl group.
+ MOP:0005353
+ has_participant: CHEBI:33494
+ C-nucleosidylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nucleosidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a guanosyl group.
+ MOP:0005354
+ has_participant: CHEBI:24459
+ C-guanosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a guanosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an inosyl group.
+ MOP:0005355
+ has_participant: CHEBI:24849
+ C-inosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an inosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a thymidyl group.
+ MOP:0005356
+ has_participant: CHEBI:27002
+ C-thymidylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a thymidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an adenosyl group.
+ MOP:0005357
+ has_participant: CHEBI:33505
+ C-adenosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an adenosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-adenosyl group.
+ MOP:0005358
+ has_participant: CHEBI:22261
+ C-5'-adenosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 5'-adenosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an uridyl group.
+ MOP:0005359
+ has_participant: CHEBI:27243
+ C-uridylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an uridyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cytidyl group.
+ MOP:0005360
+ has_participant: CHEBI:23525
+ C-cytidylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cytidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a dolichyl group.
+ MOP:0005361
+ has_participant: CHEBI:23883
+ C-dolichylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a dolichyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-trans,6-trans-farnesyl group.
+ MOP:0005362
+ has_participant: CHEBI:36535
+ C-2-trans,6-trans-farnesylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-trans,6-trans-farnesyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a margaryl group.
+ MOP:0005363
+ has_participant: CHEBI:32925
+ C-margarylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a margaryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a methyl group.
+ MOP:0005364
+ has_participant: CHEBI:32875
+ C-methylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a methyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a methanetetrayl group.
+ MOP:0005365
+ has_participant: CHEBI:30039
+ C-methanetetraylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a methanetetrayl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a methanetriyl group.
+ MOP:0005366
+ has_participant: CHEBI:29433
+ C-methanetriylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a methanetriyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trichloromethyl group.
+ MOP:0005367
+ has_participant: CHEBI:30736
+ C-trichloromethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trichloromethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trifluoromethyl group.
+ MOP:0005368
+ has_participant: CHEBI:50127
+ C-trifluoromethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trifluoromethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alkyl group.
+ MOP:0005369
+ has_participant: CHEBI:22323
+ C-alkylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a butyl group.
+ MOP:0005370
+ has_participant: CHEBI:41264
+ C-butylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a ceryl group.
+ MOP:0005371
+ has_participant: CHEBI:23081
+ C-cerylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a ceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a decyl group.
+ MOP:0005372
+ has_participant: CHEBI:23580
+ C-decylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a decyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a dodecyl group.
+ MOP:0005373
+ has_participant: CHEBI:23870
+ C-dodecylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a dodecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a heptyl group.
+ MOP:0005374
+ has_participant: CHEBI:24526
+ C-heptylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a heptyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a hexyl group.
+ MOP:0005375
+ has_participant: CHEBI:24593
+ C-hexylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a hexyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a myricyl group.
+ MOP:0005376
+ has_participant: CHEBI:25453
+ C-myricylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a myricyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a myristyl group.
+ MOP:0005377
+ has_participant: CHEBI:25457
+ C-myristylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a myristyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nonyl group.
+ MOP:0005378
+ has_participant: CHEBI:25589
+ C-nonylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an octyl group.
+ MOP:0005379
+ has_participant: CHEBI:25657
+ C-octylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an octyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a palmityl group.
+ MOP:0005380
+ has_participant: CHEBI:25842
+ C-palmitylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a palmityl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pentyl group.
+ MOP:0005381
+ has_participant: CHEBI:25902
+ C-pentylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a propyl group.
+ MOP:0005382
+ has_participant: CHEBI:26308
+ C-propylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a propyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a stearyl group.
+ MOP:0005383
+ has_participant: CHEBI:26755
+ C-stearylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a stearyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an isopropyl group.
+ MOP:0005384
+ has_participant: CHEBI:30353
+ C-isopropylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an isopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an ethyl group.
+ MOP:0005385
+ has_participant: CHEBI:37807
+ C-ethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an ethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an isobutyl group.
+ MOP:0005386
+ has_participant: CHEBI:30356
+ C-isobutylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an isobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pentan-2-yl group.
+ MOP:0005387
+ has_participant: CHEBI:32880
+ C-pentan-2-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pentan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an isopentyl group.
+ MOP:0005388
+ has_participant: CHEBI:30359
+ C-isopentylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an isopentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 3-methylbutan-2-yl group.
+ MOP:0005389
+ has_participant: CHEBI:32882
+ C-3-methylbutan-2-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 3-methylbutan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tert-pentyl group.
+ MOP:0005390
+ has_participant: CHEBI:30360
+ C-tert-pentylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tert-pentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a neopentyl group.
+ MOP:0005391
+ has_participant: CHEBI:30357
+ C-neopentylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a neopentyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an undecyl group.
+ MOP:0005392
+ has_participant: CHEBI:32900
+ C-undecylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an undecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tridecyl group.
+ MOP:0005393
+ has_participant: CHEBI:32908
+ C-tridecylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tridecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pentadecyl group.
+ MOP:0005394
+ has_participant: CHEBI:32909
+ C-pentadecylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pentadecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nonadecyl group.
+ MOP:0005395
+ has_participant: CHEBI:32928
+ C-nonadecylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nonadecyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arachidyl group.
+ MOP:0005396
+ has_participant: CHEBI:32930
+ C-arachidylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arachidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a henicosyl group.
+ MOP:0005397
+ has_participant: CHEBI:32932
+ C-henicosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a henicosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a behenyl group.
+ MOP:0005398
+ has_participant: CHEBI:32933
+ C-behenylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a behenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tricosyl group.
+ MOP:0005399
+ has_participant: CHEBI:32935
+ C-tricosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tricosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a lignoceryl group.
+ MOP:0005400
+ has_participant: CHEBI:32937
+ C-lignocerylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a lignoceryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pentacosyl group.
+ MOP:0005401
+ has_participant: CHEBI:32939
+ C-pentacosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pentacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a heptacosyl group.
+ MOP:0005402
+ has_participant: CHEBI:32942
+ C-heptacosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a heptacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a montanyl group.
+ MOP:0005403
+ has_participant: CHEBI:32944
+ C-montanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a montanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nonacosyl group.
+ MOP:0005404
+ has_participant: CHEBI:32945
+ C-nonacosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nonacosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sec-butyl group.
+ MOP:0005405
+ has_participant: CHEBI:45557
+ C-sec-butylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sec-butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tert-butyl group.
+ MOP:0005406
+ has_participant: CHEBI:30355
+ C-tert-butylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tert-butyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pentan-3-yl group.
+ MOP:0005407
+ has_participant: CHEBI:32881
+ C-pentan-3-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a pentan-3-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-chloroethyl group.
+ MOP:0005408
+ has_participant: CHEBI:47553
+ C-2-chloroethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-chloroethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 1-chloroethyl group.
+ MOP:0005409
+ has_participant: CHEBI:48099
+ C-1-chloroethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 1-chloroethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a hydrocarbyl group.
+ MOP:0005410
+ has_participant: CHEBI:33248
+ C-hydrocarbylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a hydrocarbyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an aryl group.
+ MOP:0005411
+ has_participant: CHEBI:33338
+ C-arylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an aryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phenyl group.
+ MOP:0005412
+ has_participant: CHEBI:30396
+ C-phenylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a biphenyl-4-yl group.
+ MOP:0005413
+ has_participant: CHEBI:35447
+ C-biphenyl-4-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a biphenyl-4-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a naphthyl group.
+ MOP:0005414
+ has_participant: CHEBI:51140
+ C-naphthylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 1-naphthyl group.
+ MOP:0005415
+ has_participant: CHEBI:51138
+ C-1-naphthylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 1-naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-naphthyl group.
+ MOP:0005416
+ has_participant: CHEBI:51139
+ C-2-naphthylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-naphthyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cycloalkyl group.
+ MOP:0005417
+ has_participant: CHEBI:33441
+ C-cycloalkylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cycloalkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cyclobutyl group.
+ MOP:0005418
+ has_participant: CHEBI:30376
+ C-cyclobutylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cyclobutyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cyclopropyl group.
+ MOP:0005419
+ has_participant: CHEBI:30364
+ C-cyclopropylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cyclopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alkenyl group.
+ MOP:0005420
+ has_participant: CHEBI:37614
+ C-alkenylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alkenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an oleyl group.
+ MOP:0005421
+ has_participant: CHEBI:25670
+ C-oleylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an oleyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an allyl group.
+ MOP:0005422
+ has_participant: CHEBI:30361
+ C-allylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an allyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an isopropenyl group.
+ MOP:0005423
+ has_participant: CHEBI:30354
+ C-isopropenylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an isopropenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a vinyl group.
+ MOP:0005424
+ has_participant: CHEBI:37603
+ C-vinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a vinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a prenyl group.
+ MOP:0005427
+ MOP:0005425
+ has_participant: CHEBI:26248
+ C-prenylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a prenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phytyl group.
+ MOP:0005426
+ has_participant: CHEBI:26126
+ C-phytylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phytyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a polyprenyl group.
+ MOP:0005428
+ has_participant: CHEBI:26201
+ C-polyprenylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a polyprenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a farnesyl group.
+ MOP:0005429
+ has_participant: CHEBI:24017
+ C-farnesylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a farnesyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a geranyl group.
+ MOP:0005430
+ has_participant: CHEBI:24224
+ C-geranylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a geranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a geranylgeranyl group.
+ MOP:0005431
+ has_participant: CHEBI:24231
+ C-geranylgeranylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a geranylgeranyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a retinyl group.
+ MOP:0005432
+ has_participant: CHEBI:26541
+ C-retinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a retinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an adamantan-2-yl group.
+ MOP:0005433
+ has_participant: CHEBI:48078
+ C-adamantan-2-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an adamantan-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cycloalkenyl group.
+ MOP:0005434
+ has_participant: CHEBI:48886
+ C-cycloalkenylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cycloalkenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a campholenic cyclohexenyl group.
+ MOP:0005435
+ has_participant: CHEBI:48885
+ C-campholenic cyclohexenylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a campholenic cyclohexenyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cyclopentadienyl group.
+ MOP:0005436
+ has_participant: CHEBI:30663
+ C-cyclopentadienylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an eta(5)-cyclopentadienyl group.
+ MOP:0005437
+ has_participant: CHEBI:36763
+ C-eta(5)-cyclopentadienylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an eta(5)-cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an eta(1)-cyclopentadienyl group.
+ MOP:0005438
+ has_participant: CHEBI:36764
+ C-eta(1)-cyclopentadienylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an eta(1)-cyclopentadienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an ethene-1,2-diyl group.
+ MOP:0005439
+ has_participant: CHEBI:46880
+ C-ethene-1,2-diylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an ethene-1,2-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arachidonyl group.
+ MOP:0005440
+ has_participant: CHEBI:22612
+ C-arachidonylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arachidonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a benzyl group.
+ MOP:0005441
+ has_participant: CHEBI:22744
+ C-benzylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a benzyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an anthracen-1-yl group.
+ MOP:0005442
+ has_participant: CHEBI:48287
+ C-anthracen-1-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an anthracen-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an anthracen-2-yl group.
+ MOP:0005443
+ has_participant: CHEBI:48371
+ C-anthracen-2-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an anthracen-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an imidazolyl group.
+ MOP:0005444
+ has_participant: CHEBI:50052
+ C-imidazolylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an imidazolyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an imidazol-1-yl group.
+ MOP:0005445
+ has_participant: CHEBI:50053
+ C-imidazol-1-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an imidazol-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an imidazol-2-yl group.
+ MOP:0005446
+ has_participant: CHEBI:50054
+ C-imidazol-2-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an imidazol-2-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an imidazol-5-yl group.
+ MOP:0005447
+ has_participant: CHEBI:50055
+ C-imidazol-5-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an imidazol-5-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an imidazol-4-yl group.
+ MOP:0005448
+ has_participant: CHEBI:50056
+ C-imidazol-4-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an imidazol-4-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a furyl group.
+ MOP:0005449
+ has_participant: CHEBI:24131
+ C-furylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-furyl group.
+ MOP:0005450
+ has_participant: CHEBI:19586
+ C-2-furylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 3-furyl group.
+ MOP:0005451
+ has_participant: CHEBI:20025
+ C-3-furylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 3-furyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a thienyl group.
+ MOP:0005452
+ has_participant: CHEBI:37991
+ C-thienylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-thienyl group.
+ MOP:0005453
+ has_participant: CHEBI:35849
+ C-2-thienylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 3-thienyl group.
+ MOP:0005454
+ has_participant: CHEBI:37992
+ C-3-thienylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 3-thienyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an adenin-9-yl group.
+ MOP:0005455
+ has_participant: CHEBI:30756
+ C-adenin-9-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an adenin-9-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a guanin-9-yl group.
+ MOP:0005456
+ has_participant: CHEBI:30755
+ C-guanin-9-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a guanin-9-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acetimidoyl group.
+ MOP:0005457
+ has_participant: CHEBI:48050
+ C-acetimidoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acetimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an organyl group.
+ MOP:0005458
+ has_participant: CHEBI:33249
+ C-organylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an organyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an organic heterocyclyl group.
+ MOP:0005459
+ has_participant: CHEBI:33453
+ C-organic heterocyclylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an organic heterocyclyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a heteroaryl group.
+ MOP:0005460
+ has_participant: CHEBI:33470
+ C-heteroarylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a heteroaryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 4,4'-dimethoxytriphenylmethyl group.
+ MOP:0005461
+ has_participant: CHEBI:51095
+ C-4,4'-dimethoxytriphenylmethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 4,4'-dimethoxytriphenylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tauryl group.
+ MOP:0005462
+ has_participant: CHEBI:26861
+ C-taurylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tauryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a triflyl group.
+ MOP:0005463
+ has_participant: CHEBI:48548
+ C-triflylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a triflyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glycidyl group.
+ MOP:0005464
+ has_participant: CHEBI:24366
+ C-glycidylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a glycidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfanylmethyl group.
+ MOP:0005465
+ has_participant: CHEBI:50326
+ C-sulfanylmethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfanylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a selanylmethyl group.
+ MOP:0005466
+ has_participant: CHEBI:50327
+ C-selanylmethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a selanylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-carboxyethyl group.
+ MOP:0005467
+ has_participant: CHEBI:50329
+ C-2-carboxyethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-carboxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-amino-2-oxoethyl group.
+ MOP:0005468
+ has_participant: CHEBI:50330
+ C-2-amino-2-oxoethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-amino-2-oxoethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 3-amino-3-oxopropyl group.
+ MOP:0005469
+ has_participant: CHEBI:50331
+ C-3-amino-3-oxopropylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 3-amino-3-oxopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-(methylsulfanyl)ethyl group.
+ MOP:0005470
+ has_participant: CHEBI:50332
+ C-2-(methylsulfanyl)ethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-(methylsulfanyl)ethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 4-hydroxybenzyl group.
+ MOP:0005471
+ has_participant: CHEBI:50336
+ C-4-hydroxybenzylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 4-hydroxybenzyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 1H-indol-3-ylmethyl group.
+ MOP:0005472
+ has_participant: CHEBI:50337
+ C-1H-indol-3-ylmethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 1H-indol-3-ylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 1H-imidazol-4-ylmethyl group.
+ MOP:0005473
+ has_participant: CHEBI:50338
+ C-1H-imidazol-4-ylmethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 1H-imidazol-4-ylmethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 3-carbamimidamidopropyl group.
+ MOP:0005474
+ has_participant: CHEBI:50340
+ C-3-carbamimidamidopropylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 3-carbamimidamidopropyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a hydroxymethyl group.
+ MOP:0005475
+ has_participant: CHEBI:24712
+ C-hydroxymethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a hydroxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 1-hydroxyethyl group.
+ MOP:0005476
+ has_participant: CHEBI:50341
+ C-1-hydroxyethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 1-hydroxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a haloalkyl group.
+ MOP:0005477
+ has_participant: CHEBI:50491
+ C-haloalkylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a haloalkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-(trimethylsilyl)ethoxymethyl group.
+ MOP:0005478
+ has_participant: CHEBI:51093
+ C-2-(trimethylsilyl)ethoxymethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-(trimethylsilyl)ethoxymethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acyl group.
+ MOP:0005479
+ has_participant: CHEBI:22221
+ C-acylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an organoheteryl group.
+ MOP:0005480
+ has_participant: CHEBI:33456
+ C-organoheterylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an organoheteryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an oxalosulfanyl group.
+ MOP:0005481
+ has_participant: CHEBI:30874
+ C-oxalosulfanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an oxalosulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an organosilyl group.
+ MOP:0005482
+ has_participant: CHEBI:33478
+ C-organosilylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an organosilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trimethylsilyl group.
+ MOP:0005483
+ has_participant: CHEBI:51088
+ C-trimethylsilylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trimethylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a triisopropylsilyl group.
+ MOP:0005484
+ has_participant: CHEBI:51089
+ C-triisopropylsilylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a triisopropylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tert-butyldiphenylsilyl group.
+ MOP:0005485
+ has_participant: CHEBI:51090
+ C-tert-butyldiphenylsilylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tert-butyldiphenylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tert-butyldimethylsilyl group.
+ MOP:0005486
+ has_participant: CHEBI:51091
+ C-tert-butyldimethylsilylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tert-butyldimethylsilyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a thioacyl group.
+ MOP:0005487
+ has_participant: CHEBI:49063
+ C-thioacylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a thioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carbothioacyl group.
+ MOP:0005488
+ has_participant: CHEBI:49066
+ C-carbothioacylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an univalent carbothioacyl group.
+ MOP:0005489
+ has_participant: CHEBI:49067
+ C-univalent carbothioacylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an univalent carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a divalent carbothioacyl group.
+ MOP:0005490
+ has_participant: CHEBI:49068
+ C-divalent carbothioacylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a divalent carbothioacyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carbonimidoyl group.
+ MOP:0005491
+ has_participant: CHEBI:29815
+ C-carbonimidoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carbonimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a thiocarbonyl group.
+ MOP:0005492
+ has_participant: CHEBI:30256
+ C-thiocarbonylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a thiocarbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a (fluoren-9-ylmethoxy)carbonyl group.
+ MOP:0005493
+ has_participant: CHEBI:48605
+ C-(fluoren-9-ylmethoxy)carbonylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a (fluoren-9-ylmethoxy)carbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carbonyl group.
+ MOP:0005494
+ has_participant: CHEBI:23019
+ C-carbonylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a carbonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cytosin-1-yl group.
+ MOP:0005495
+ has_participant: CHEBI:30758
+ C-cytosin-1-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a cytosin-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a thymin-1-yl group.
+ MOP:0005496
+ has_participant: CHEBI:30757
+ C-thymin-1-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a thymin-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an uracil-1-yl group.
+ MOP:0005497
+ has_participant: CHEBI:30759
+ C-uracil-1-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an uracil-1-yl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a morpholin-4-ylsulfonyl group.
+ MOP:0005498
+ has_participant: CHEBI:45701
+ C-morpholin-4-ylsulfonylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a morpholin-4-ylsulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acetohydrazonoyl group.
+ MOP:0005499
+ has_participant: CHEBI:48054
+ C-acetohydrazonoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acetohydrazonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-hydroxyethyl group.
+ MOP:0005500
+ has_participant: CHEBI:44730
+ C-2-hydroxyethylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a 2-hydroxyethyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an aminosulfinyl group.
+ MOP:0005501
+ has_participant: CHEBI:48257
+ C-aminosulfinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an aminosulfinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a disiloxanyl group.
+ MOP:0005502
+ has_participant: CHEBI:48142
+ C-disiloxanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a disiloxanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a disiloxane-1,3-diyl group.
+ MOP:0005503
+ has_participant: CHEBI:48143
+ C-disiloxane-1,3-diylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a disiloxane-1,3-diyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an azinoyl group.
+ MOP:0005504
+ has_participant: CHEBI:29771
+ C-azinoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an azinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an azonoyl group.
+ MOP:0005505
+ has_participant: CHEBI:37768
+ C-azonoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an azonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phosphorothioyl group.
+ MOP:0005506
+ has_participant: CHEBI:32412
+ C-phosphorothioylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phosphorothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phosphonothioyl group.
+ MOP:0005507
+ has_participant: CHEBI:32413
+ C-phosphonothioylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phosphonothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arsonoyl group.
+ MOP:0005508
+ has_participant: CHEBI:29848
+ C-arsonoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arsonoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arsinoyl group.
+ MOP:0005509
+ has_participant: CHEBI:30277
+ C-arsinoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arsinoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a stiboryl group.
+ MOP:0005510
+ has_participant: CHEBI:48439
+ C-stiborylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a stiboryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfamoyl group.
+ MOP:0005511
+ has_participant: CHEBI:48266
+ C-sulfamoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfamoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a S-aminosulfinimidoyl group.
+ MOP:0005512
+ has_participant: CHEBI:48254
+ C-S-aminosulfinimidoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a S-aminosulfinimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a S-aminosulfonimidoyl group.
+ MOP:0005513
+ has_participant: CHEBI:48264
+ C-S-aminosulfonimidoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a S-aminosulfonimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a chloryl group.
+ MOP:0005514
+ has_participant: CHEBI:29883
+ C-chlorylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a chloryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a chlorosyl group.
+ MOP:0005515
+ has_participant: CHEBI:29878
+ C-chlorosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a chlorosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a perchloryl group.
+ MOP:0005516
+ has_participant: CHEBI:29877
+ C-perchlorylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a perchloryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a bromosyl group.
+ MOP:0005517
+ has_participant: CHEBI:29871
+ C-bromosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a bromosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a bromyl group.
+ MOP:0005518
+ has_participant: CHEBI:29881
+ C-bromylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a bromyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a perbromyl group.
+ MOP:0005519
+ has_participant: CHEBI:29891
+ C-perbromylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a perbromyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an iodosyl group.
+ MOP:0005520
+ has_participant: CHEBI:29897
+ C-iodosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an iodosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an iodyl group.
+ MOP:0005521
+ has_participant: CHEBI:29904
+ C-iodylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an iodyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a periodyl group.
+ MOP:0005522
+ has_participant: CHEBI:29908
+ C-periodylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a periodyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a fluorosyl group.
+ MOP:0005523
+ has_participant: CHEBI:30241
+ C-fluorosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a fluorosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfonyl group.
+ MOP:0005539
+ MOP:0005524
+ has_participant: CHEBI:29825
+ C-sulfonylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acetoxysulfonyl group.
+ MOP:0005525
+ has_participant: CHEBI:48065
+ C-acetoxysulfonylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an acetoxysulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfonothioyl group.
+ MOP:0005526
+ has_participant: CHEBI:29828
+ C-sulfonothioylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfonothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfinothioyl group.
+ MOP:0005527
+ has_participant: CHEBI:29827
+ C-sulfinothioylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfinothioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfonodithioyl group.
+ MOP:0005528
+ has_participant: CHEBI:29835
+ C-sulfonodithioylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfonodithioyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trioxidanyl group.
+ MOP:0005529
+ has_participant: CHEBI:29791
+ C-trioxidanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trioxidanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trioxidanediyl group.
+ MOP:0005530
+ has_participant: CHEBI:30493
+ C-trioxidanediylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a trioxidanediyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a heterocyclyl group.
+ MOP:0005531
+ has_participant: CHEBI:48271
+ C-heterocyclylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a heterocyclyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phosphoramidochloridoyl group.
+ MOP:0005532
+ has_participant: CHEBI:48229
+ C-phosphoramidochloridoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a phosphoramidochloridoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a S-aminosulfonodiimidoyl group.
+ MOP:0005533
+ has_participant: CHEBI:48265
+ C-S-aminosulfonodiimidoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a S-aminosulfonodiimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an aminosulfanyl group.
+ MOP:0005534
+ has_participant: CHEBI:48252
+ C-aminosulfanylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an aminosulfanyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfinyl group.
+ MOP:0005535
+ has_participant: CHEBI:29822
+ C-sulfinylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfinyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arsoryl group.
+ MOP:0005536
+ has_participant: CHEBI:30274
+ C-arsorylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an arsoryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an azanediidyl group.
+ MOP:0005537
+ has_participant: CHEBI:30227
+ C-azanediidylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an azanediidyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfinimidoyl group.
+ MOP:0005538
+ has_participant: CHEBI:29829
+ C-sulfinimidoylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfinimidoyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tosyl group.
+ MOP:0005540
+ has_participant: CHEBI:51094
+ C-tosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a tosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a brosyl group.
+ MOP:0005541
+ has_participant: CHEBI:51101
+ C-brosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a brosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nosyl group.
+ MOP:0005542
+ has_participant: CHEBI:51102
+ C-nosylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nosyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an indolyl group.
+ MOP:0005544
+ has_participant: CHEBI:51609
+ C-indolylamination
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an indolyl group.
+ RSC:xp
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an indol-1-yl group.
+ MOP:0005545
+ has_participant: CHEBI:51610
+ C-indol-1-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an indol-1-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an indol-2-yl group.
+ MOP:0005546
+ has_participant: CHEBI:51611
+ C-indol-2-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an indol-2-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an indol-3-yl group.
+ MOP:0005547
+ has_participant: CHEBI:51612
+ C-indol-3-ylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an indol-3-yl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-oxindolyl group.
+ MOP:0005548
+ has_participant: CHEBI:51613
+ C-N-oxindolylation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an N-oxindolyl group.
+ rsc:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alkylamino group.
+ MOP:0005549
+ has_participant: CHEBI:22332
+ C-alkylamination
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an alkylamino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a halo group.
+ MOP:0005550
+ has_participant: CHEBI:47854
+ C-halogenation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a halo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a bromo group.
+ MOP:0005551
+ has_participant: CHEBI:47265
+ C-bromination
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a bromo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a chloro group.
+ MOP:0005552
+ has_participant: CHEBI:47853
+ C-chlorination
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a chloro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a fluoro group.
+ MOP:0005553
+ has_participant: CHEBI:42645
+ C-fluorination
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a fluoro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an iodo group.
+ MOP:0005554
+ has_participant: CHEBI:43448
+ C-iodination
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an iodo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an imino group.
+ MOP:0005555
+ has_participant: CHEBI:29342
+ C-imination
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and an imino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nitro group.
+ MOP:0005556
+ has_participant: CHEBI:29785
+ C-nitration
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a nitro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a hydroxyamino group.
+ MOP:0005557
+ has_participant: CHEBI:29769
+ C-hydroxyamination
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a hydroxyamino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a thioxo group.
+ MOP:0005558
+ has_participant: CHEBI:29833
+ C-thioxonation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a thioxo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfo group.
+ MOP:0005559
+ has_participant: CHEBI:29922
+ C-sulfonation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a sulfo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a selenono group.
+ MOP:0005560
+ has_participant: CHEBI:29923
+ C-selenonation
+
+
+
+
+ Formation of a covalent bond between a carbon atom in a substrate and a selenono group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
diff --git a/src/rxno.owl b/src/rxno.owl
new file mode 100644
index 0000000..923a6a4
--- /dev/null
+++ b/src/rxno.owl
@@ -0,0 +1,23394 @@
+
+
+
+
+
+ RXNO is the name reaction ontology. It contains more than 500 classes representing organic reactions such as the Diels–Alder cyclization.
+ RXNO
+
+ 16:12:2021 15:55
+ RXNO
+ 1.4
+
+
+
+
+
+
+
+
+
+
+
+
+ definition
+
+
+
+
+
+
+
+
+
+
+
+
+
+ imported from
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ has_alternative_id
+
+
+
+
+
+
+
+ has_broad_synonym
+
+
+
+
+
+
+
+ database_cross_reference
+
+
+
+
+
+
+
+ has_exact_synonym
+
+
+
+
+
+
+
+ has_narrow_synonym
+
+
+
+
+
+
+
+ has_obo_format_version
+
+
+
+
+
+
+
+ has_obo_namespace
+
+
+
+
+
+
+
+ has_related_synonym
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ in_subset
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ RXNO
+ BFO:0000055
+ realizes
+
+
+
+
+
+
+
+ RXNO
+ BFO:0000057
+ has_participant
+
+
+
+
+
+
+
+
+ RXNO
+ BFO:0000077
+ has participant beginning to exist
+
+
+
+
+
+
+
+
+ RXNO
+ BFO:0000078
+ has participant ceasing to exist
+
+
+
+
+
+
+
+ RXNO
+ BFO:0000162
+ has disposition at all times
+
+
+
+
+
+
+
+
+
+ This relation obtains between a planned process and a objective specification when the criteria specified in the objective specification are met at the end of the planned process.
+ RXNO
+ OBI:0000417
+ achieves_planned_objective
+
+
+
+
+ This relation obtains between a planned process and a objective specification when the criteria specified in the objective specification are met at the end of the planned process.
+ obi:AR
+ obi:BP
+ obi:PPPBbranch
+
+
+
+
+
+
+
+
+
+
+ The notion here is that a given reaction is meant to 'protect' a given group from reacting in a subsequent process and can be 'deprotected' later.
+ RXNO
+ RXNO:0000416
+ can we chain 'has specified reactant' (RXNO:0000424) and has_part ?
+ protects
+
+
+
+
+ The notion here is that a given reaction is meant to 'protect' a given group from reacting in a subsequent process and can be 'deprotected' later.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+ If a reaction R deprotects a group G, then G is in the product where it wasn't in the reactant.
+ RXNO
+ RXNO:0000417
+ can we chain 'has specified product' (RXNO:0000423) and has_part ?
+ deprotects
+
+
+
+
+ If a reaction R deprotects a group G, then G is in the product where it wasn't in the reactant.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+ A relation between a planned reaction step and a molecular entity participating in that process. The creation of the molecular entity during the process is explicitly specified in the objective specification which the planned reaction step realizes the concretization of.
+ RXNO
+ RXNO:0000423
+ The difference between this and OBI's has_specified_output is that it is necessary that the participant starts to exist during the process.
+ has specified product
+
+
+
+
+ A relation between a planned reaction step and a molecular entity participating in that process. The creation of the molecular entity during the process is explicitly specified in the objective specification which the planned reaction step realizes the concretization of.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+ A relation between a planned reaction step and a molecular entity participating in that process that is not created during the process. The destruction of the molecular entity during the process is explicitly specified in the plan specification which the process realizes the concretization of.
+ RXNO
+ RXNO:0000424
+ The difference between this and OBI's has_specified_input is that it is necessary that the reactant ceases to exist during the process.
+ has specified reactant
+
+
+
+
+ A relation between a planned reaction step and a molecular entity participating in that process that is not created during the process. The destruction of the molecular entity during the process is explicitly specified in the plan specification which the process realizes the concretization of.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A relation between a planned reaction step and a molecular entity participating in that process that has_role catalyst ((CHEBI:35223).
+ RXNO
+ RXNO:0000425
+ has_catalyst
+
+
+
+
+ A relation between a planned reaction step and a molecular entity participating in that process that has_role catalyst ((CHEBI:35223).
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A relation between a planned reaction step and a molecular entity participating in that process. The creation and subsequent destruction of the molecular entity during the process are explicitly specified in the plan specification which the process realizes the concretization of.
+ RXNO
+ RXNO:0000469
+ has_intermediate
+
+
+
+
+ A relation between a planned reaction step and a molecular entity participating in that process. The creation and subsequent destruction of the molecular entity during the process are explicitly specified in the plan specification which the process realizes the concretization of.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+ RXNO
+ has_part
+ has_part
+
+
+
+
+
+
+
+ RXNO
+ part_of
+ part_of
+
+
+
+
+
+
+
+
+
+
+
+
+ RXNO
+ BFO:0000015
+ process
+
+
+
+
+
+
+
+ RXNO
+ BFO:0000016
+ disposition
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:13759
+ alkylamine
+
+
+
+
+
+
+
+
+ An alpha-oxyketone that has a hydroxy group as the alpha-oxy moiety.
+ http://purl.obolibrary.org/obo/chebi/205/chebi.owl
+ chebi_ontology
+ CHEBI:139588
+
+ alpha-hydroxy ketone
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:15379
+ dioxygen
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:15734
+ primary alcohol
+
+
+
+
+
+
+
+
+ An organic hydroxy compound that consists of benzene bearing a single hydroxy substituent. The parent of the class of phenols.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ CHEBI:14777
+ CHEBI:25966
+ CHEBI:43543
+ CHEBI:8071
+ chebi_ontology
+ CHEBI:15882
+
+ phenol
+
+
+
+
+
+
+
+
+ An azane that consists of a single nitrogen atom covelently bonded to three hydrogen atoms.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ CHEBI:13405
+ CHEBI:13406
+ CHEBI:13407
+ CHEBI:13771
+ CHEBI:22533
+ CHEBI:44269
+ CHEBI:44284
+ CHEBI:44404
+ CHEBI:7434
+ chebi_ontology
+ CHEBI:16134
+
+ ammonia
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:16227
+ pyridine
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:16240
+ hydrogen peroxide
+
+
+
+
+
+
+
+
+ Compounds having the structure RSR (R =/= H). Such compounds were once called thioethers.
+ CHEBI:13694
+ CHEBI:26960
+ CHEBI:9340
+ chebi_ontology
+ CHEBI:16385
+
+ organic sulfide
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:16526
+ carbon dioxide
+
+
+
+
+
+
+
+
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ CHEBI:14137
+ CHEBI:23664
+ CHEBI:4486
+ chebi_ontology
+ CHEBI:16648
+
+ dialkyl phosphate
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:16670
+ peptide
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:16842
+ formaldehyde
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:17087
+ ketone
+
+
+
+
+
+
+
+
+ A one-carbon compound in which the carbon is joined only to a single oxygen. It is a colourless, odourless, tasteless, toxic gas.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ CHEBI:13281
+ CHEBI:23013
+ CHEBI:3282
+ CHEBI:41526
+ chebi_ontology
+ CHEBI:17245
+
+ carbon monoxide
+
+
+
+
+
+
+
+
+ An organosilicon compound that is benzene in which a hydrogen is replaced by a silyl group.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:172874
+
+ phenylsilane
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:17478
+ aldehyde
+
+
+
+
+
+
+
+
+ A compound containing at least one carbon-halogen bond (where X is a halogen atom).
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ CHEBI:13444
+ CHEBI:36684
+ CHEBI:8767
+ chebi_ontology
+ CHEBI:17792
+
+ organohalogen compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:17883
+ hydrogen chloride
+
+
+
+
+
+
+
+
+ An elemental molecule consisting of two trivalently-bonded nitrogen atoms.
+ 0
+ N2
+ InChI=1S/N2/c1-2
+ IJGRMHOSHXDMSA-UHFFFAOYSA-N
+ 28.01348
+ 28.00615
+ N#N
+ CHEBI:13388
+ CHEBI:14660
+ CHEBI:25365
+ CHEBI:43128
+ CHEBI:7593
+ CAS:7727-37-9
+ Drug_Central:4251
+ Gmelin:150
+ HMDB:HMDB0001371
+ KEGG:C00697
+ KEGG:D00083
+ MetaCyc:NITROGEN-MOLECULE
+ PDBeChem:HDZ
+ PMID:18334638
+ PMID:22237545
+ Reaxys:15940095
+ Wikipedia:Nitrogen
+ dinitrogen
+ chebi_ontology
+ N#N
+ N2
+ Nitrogen
+ molecular nitrogen
+ CHEBI:17997
+
+ dinitrogen
+
+
+
+
+ CAS:7727-37-9
+ NIST Chemistry WebBook
+
+
+
+
+ Drug_Central:4251
+ DrugCentral
+
+
+
+
+ Gmelin:150
+ Gmelin
+
+
+
+
+ PMID:18334638
+ Europe PMC
+
+
+
+
+ PMID:22237545
+ Europe PMC
+
+
+
+
+ Reaxys:15940095
+ Reaxys
+
+
+
+
+ dinitrogen
+ IUPAC
+
+
+
+
+
+ N#N
+ ChEBI
+
+
+
+
+ N2
+ IUPAC
+
+
+
+
+ N2
+ KEGG_COMPOUND
+
+
+
+
+ N2
+ UniProt
+
+
+
+
+ Nitrogen
+ KEGG_COMPOUND
+
+
+
+
+ molecular nitrogen
+ ChEBI
+
+
+
+
+ CAS:7727-37-9
+ ChemIDplus
+
+
+
+
+ CAS:7727-37-9
+ KEGG COMPOUND
+
+
+
+
+
+
+
+
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ CHEBI:13368
+ CHEBI:37140
+ CHEBI:5599
+ chebi_ontology
+ CHEBI:18140
+
+ hydrogen halide
+
+
+
+
+
+
+
+
+ A manganese group element atom that has formula Mn.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ CHEBI:13382
+ CHEBI:25153
+ CHEBI:6681
+ chebi_ontology
+ CHEBI:18291
+
+ manganese atom
+
+
+
+
+
+
+
+
+ An acyclic branched or unbranched hydrocarbon having the general formula CnH2n+2, and therefore consisting entirely of hydrogen atoms and saturated carbon atoms.
+ 0
+ CH3R
+ 15.035
+ 15.02348
+ C[*]
+ CHEBI:13435
+ CHEBI:22317
+ CHEBI:2576
+ KEGG:C01371
+ Alkane
+ alkane
+ alkanes
+ chebi_ontology
+ Alkan
+ RH
+ alcane
+ alcanes
+ alcano
+ alcanos
+ an alkane
+ CHEBI:18310
+
+ alkane
+
+
+
+
+ Alkane
+ KEGG_COMPOUND
+
+
+
+
+ alkane
+ IUPAC
+
+
+
+
+
+ alkanes
+ IUPAC
+
+
+
+
+
+ Alkan
+ ChEBI
+
+
+
+
+ RH
+ KEGG_COMPOUND
+
+
+
+
+ alcane
+ IUPAC
+
+
+
+
+ alcanes
+ IUPAC
+
+
+
+
+ alcano
+ IUPAC
+
+
+
+
+ alcanos
+ IUPAC
+
+
+
+
+ an alkane
+ UniProt
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:18379
+ nitrile
+
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:22213
+ acridines
+
+
+
+
+
+
+
+
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:22324
+
+ alkyl phosphate
+
+
+
+
+
+
+
+
+ Acyclic branched or unbranched hydrocarbons having a carbon-carbon triple bond and the general formula CnH2n-2, RC#CR.
+ chebi_ontology
+ CHEBI:22339
+
+ alkyne
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33855
+ arenecarbaldehyde
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:22680
+ azide
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:22698
+ benzaldehydes
+
+
+
+
+
+
+
+
+ Any benzenoid aromatic compound consisting of the benzene skeleton and its substituted derivatives.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:22712
+
+ benzenes
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:22715
+ benzimidazoles
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:22929
+ bromoalkane
+
+
+
+
+
+
+
+
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:23014
+
+ carbon oxide
+
+
+
+
+
+
+
+
+ 0
+ CO
+ 28.01010
+ 27.99491
+ O=C(*)*
+ carbonyl
+ carbonyl group
+ chebi_ontology
+ >C=O
+ CHEBI:23019
+
+ carbonyl group
+
+
+
+
+ carbonyl
+ IUPAC
+
+
+
+
+
+ carbonyl group
+ ChEBI
+
+
+
+
+ carbonyl group
+ UniProt
+
+
+
+
+ >C=O
+ IUPAC
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:23086
+ chalcones
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:23128
+ chloroalkane
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:23252
+ cinnamic acids
+
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:23367
+ molecular entity
+
+
+
+
+
+
+
+
+ Salts and C-organyl derivatives of hydrogen cyanide, HC#N.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:23424
+
+ cyanides
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:24043
+ flavones
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:24079
+ formamides
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:24129
+ furans
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:24431
+ chemical entity
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:24433
+ group
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:24469
+ haloalkane
+
+
+
+
+
+
+
+
+ A compound derived from a hydrocarbon by replacing a hydrogen atom with a halogen atom.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:24472
+
+ halohydrocarbon
+
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:24828
+ indoles
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:25000
+ lactone
+
+
+
+
+
+
+
+
+ Any member of the class of toluenes bearing one or more nitro substituents on the benzene ring.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:25566
+
+ nitrotoluene
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:25698
+ ether
+
+
+
+
+
+
+
+
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:25703
+
+ organic phosphate
+
+
+
+
+
+
+
+
+ A compound having bonds between one or more metal atoms and one or more carbon atoms of an organyl group.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:25707
+
+ organometallic compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:25710
+ organophosphorus compound
+
+
+
+
+
+
+
+
+ An organosilicon compound is a compound containing at least one carbon-silicon bond.
+ organosilicon compound
+ chebi_ontology
+ organosilicon compounds
+ silicoorganic compounds
+ CHEBI:25713
+
+ organosilicon compound
+
+
+
+
+ organosilicon compound
+ ChEBI
+
+
+
+
+ organosilicon compounds
+ ChEBI
+
+
+
+
+ silicoorganic compounds
+ ChEBI
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:25717
+ organotin compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:25750
+ oxime
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:25996
+ phenylhydrazine
+
+
+
+
+
+
+
+
+ Derivatives of oxoacids RnE(=O)OH in which the hydroxy group is replaced by an amino group and the oxo group is replaced by =NR. In organic chemistry an unspecified amidine is commonly a carboxamidine.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:2634
+
+ amidine
+
+
+
+
+
+
+
+
+ http://purl.obolibrary.org/obo/chebi/205/chebi.owl
+ chebi_ontology
+ CHEBI:26407
+
+ pyrans
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:26410
+ pyrazoles
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:26421
+ pyridines
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:26455
+ pyrroles
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:26513
+ quinolines
+
+
+
+
+
+
+
+
+ A molecular entity possessing an unpaired electron.
+ http://purl.obolibrary.org/obo/chebi/205/chebi.owl
+ chebi_ontology
+ CHEBI:26519
+
+ radical
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:26588
+ triazines
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:26708
+ sodium atom
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:26878
+ tertiary alcohol
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:26961
+ thiophenes
+
+
+
+
+
+
+
+
+ Any member of the class of benzenes that is a substituted benzene in which the substituents include one (and only one) methyl group.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:27024
+
+ toluenes
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:27081
+ transition element atom
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:27363
+ zinc atom
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:27385
+ tetrachloromethane
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:27539
+ isatin
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:278547
+ sodium azide
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:28112
+ nickel atom
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:28659
+ phosphorus atom
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:28694
+ copper atom
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:28802
+ flavonols
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:29224
+ dibromine
+
+
+
+
+
+
+
+
+ An organosulfur compound in which a thiol group, -SH, is attached to a carbon atom of any aliphatic or aromatic moiety.
+ CHEBI:13443
+ CHEBI:13696
+ CHEBI:17366
+ CHEBI:26969
+ CHEBI:8766
+ CHEBI:9556
+ chebi_ontology
+ CHEBI:29256
+
+ thiol
+
+
+
+
+
+
+
+
+ A sulfur hydride that has formula HS.
+ chebi_ontology
+ CHEBI:29312
+
+ sulfanyl
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:29785
+ nitro group
+
+
+
+
+
+
+
+
+ 0
+ H2N2
+ InChI=1S/H2N2/c1-2/h1-2H
+ RAABOESOVLLHRU-UHFFFAOYSA-N
+ 30.02936
+ 30.02180
+ N=N
+ CAS:3618-05-1
+ KEGG:C05360
+ diazene
+ chebi_ontology
+ Diimide
+ HN=NH
+ CHEBI:30096
+
+ diazene
+
+
+
+
+ CAS:3618-05-1
+ ChemIDplus
+
+
+
+
+ CAS:3618-05-1
+ NIST Chemistry WebBook
+
+
+
+
+ diazene
+ IUPAC
+
+
+
+
+
+ Diimide
+ NIST_Chemistry_WebBook
+
+
+
+
+ HN=NH
+ IUPAC
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:30879
+ alcohol
+
+
+
+
+
+
+
+
+ An indolinone carrying an oxo group at position 2.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:31697
+
+ indolin-2-one
+
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:32816
+ pyruvic acid
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:32863
+ secondary amine
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:32876
+ tertiary amine
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:32877
+ primary amine
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:32878
+ alkene
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:32952
+ amine
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:32955
+ epoxide
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:32988
+ amide
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33250
+ atom
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33256
+ primary amide
+
+
+
+
+
+
+
+
+ A molecular entity all atoms of which have the same atomic number.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:33259
+
+ elemental molecular entity
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33308
+ carboxylic ester
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33338
+ aryl group
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33341
+ titanium atom
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33363
+ palladium atom
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33364
+ platinum atom
+
+
+
+
+
+
+
+
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:33403
+
+ elemental sulfur
+
+
+
+
+
+
+
+
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:33434
+
+ elemental halogen
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33521
+ metal atom
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33575
+ carboxylic acid
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33595
+ cyclic compound
+
+
+
+
+
+
+
+
+ A cyclic compound having as ring members atoms of the same element only.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:33597
+
+ homocyclic compound
+
+
+
+
+
+
+
+
+ A homocyclic compound in which all of the ring members are carbon atoms.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:33598
+
+ carbocyclic compound
+
+
+
+
+
+
+
+
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:33635
+
+ polycyclic compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33641
+ olefin
+
+
+
+
+
+
+
+
+ A cyclically conjugated molecular entity with a stability (due to delocalization) significantly greater than that of a hypothetical localized structure (e.g. Kekule structure) is said to possess aromatic character.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:33655
+
+ aromatic compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33658
+ arene
+
+
+
+
+
+
+
+
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:33659
+
+ organic aromatic compound
+
+
+
+
+
+
+
+
+ A polycyclic compound in which at least one of the rings contains at least one non-carbon atom.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:33671
+
+ heteropolycyclic compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33822
+ organic hydroxy compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33823
+ enol
+
+
+
+
+
+
+
+
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:33836
+
+ benzenoid aromatic compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33839
+ macromolecule
+
+
+
+
+
+
+
+
+ A monocyclic aromatic hydrocarbon.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:33847
+
+ monocyclic arene
+
+
+
+
+
+
+
+
+ A polycyclic aromatic hydrocarbon.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:33848
+
+ polycyclic arene
+
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33853
+ phenols
+
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:33860
+ aromatic amine
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:35255
+ chloroform
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:35293
+ fused compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:35352
+ organonitrogen compound
+
+
+
+
+
+
+
+
+ The isomer HN(+)#C(-) of hydrocyanic acid, HC#N, and its hydrocarbyl derivatives RNC (RN(+)#C(-)).
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:35353
+
+ isocyanide
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:35403
+ chromium coordination entity
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:35562
+ 1,2,3-triazole
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:35636
+ carboximides
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:35681
+ secondary alcohol
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:35689
+ tetrazoles
+
+
+
+
+
+
+
+
+ A compound formally derived from an oxoacid RkE(=O)l(OH)m (l > 0) and an alcohol, phenol, heteroarenol, or enol by linking with formal loss of water from an acidic hydroxy group of the former and a hydroxy group of the latter.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ CHEBI:23960
+ CHEBI:4859
+ chebi_ontology
+ CHEBI:35701
+
+ ester
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:35715
+ nitro compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:35873
+ carboxylic anhydride
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:35886
+ tertiary phosphine
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:36587
+ carbonyl compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:36601
+ triphenylphosphane oxide
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:36605
+ phthalic anhydride
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:36606
+ acid anhydride
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:36687
+ acyl chloride
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:36823
+ pseudohalo group
+
+
+
+
+
+
+
+
+ http://purl.obolibrary.org/obo/chebi/205/chebi.owl
+ chebi_ontology
+ CHEBI:36871
+
+ inorganic radical
+
+
+
+
+
+
+
+
+ http://purl.obolibrary.org/obo/chebi/205/chebi.owl
+ chebi_ontology
+ CHEBI:36872
+
+ organic radical
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:36963
+ organooxygen compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:37148
+ bromoarene
+
+
+
+
+
+
+
+
+ Any heteroatomic molecular entity that is a chemical compound of halogen with other chemical elements.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:37578
+
+ halide
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:37579
+ acyl halide
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:37592
+ organic phosphonate
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:37602
+ allenes
+
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:37613
+ cyclohexadiene
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:37622
+ carboxamide
+
+
+
+
+
+
+
+
+ A phosphonic acid derivative in which one or both OH groups have been esterified.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ CHEBI:26068
+ CHEBI:4861
+ chebi_ontology
+ CHEBI:37735
+
+ phosphonic ester
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:37757
+ iodoalkane
+
+
+
+
+
+
+
+
+ Any of a class of cyclic chemical compounds that contain an unsaturated six-membered ring with one ring oxygen atom and an oxo substituent.
+ http://purl.obolibrary.org/obo/chebi/205/chebi.owl
+ chebi_ontology
+ CHEBI:37963
+
+ pyranone
+
+
+
+
+
+
+
+
+
+ Any organonitrogen compound containing a cyclic component with nitrogen and at least one other element as ring member atoms.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ RXNO
+ chebi_ontology
+ CHEBI:38101
+
+ organonitrogen heterocyclic compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:38104
+ oxacycle
+
+
+
+
+
+
+
+
+ thiacycle
+ RXNO
+ CHEBI:38106
+ I think this is the same as a thiacycle but need to check.
+ organosulfur heterocyclic compound
+
+
+
+
+
+
+
+
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ CHEBI:25429
+ CHEBI:38075
+ chebi_ontology
+ CHEBI:38166
+
+ organic heteropolycyclic compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:38269
+ boronic acids
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:38597
+ triazole
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:38757
+ isoflavones
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:38784
+ oxetanes
+
+
+
+
+
+
+
+
+
+ A monocyclic arene that is benzene substituted with one or more alkyl groups.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:38976
+
+ alkylbenzene
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:39141
+ Brønsted acid
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:39142
+ Brønsted base
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:39143
+ Lewis acid
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:39144
+ Lewis base
+
+
+
+
+
+
+
+
+ A haloalkane that is methane in which one (or more) of the hydrogens have been replaced by a halogen atom/halogen atoms.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:39279
+
+ halomethane
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:39447
+ pyrimidines
+
+
+
+
+
+
+
+
+ Radicals derived from hydroxylamines by removal of the hydrogen atom from the hydroxy group. The synonymous terms nitroxyl radicals and nitroxides erroneously suggest the presence of a nitro group.
+ http://purl.obolibrary.org/obo/chebi/205/chebi.owl
+ chebi_ontology
+ CHEBI:39477
+
+ aminoxyls
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:42485
+ formyl group
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:43176
+ hydroxy group
+
+
+
+
+
+
+
+
+ A dithiol that is propane substituted by thiol groups at positions 1 ans 3.
+ http://purl.obolibrary.org/obo/chebi/200/chebi.owl
+ chebi_ontology
+ CHEBI:44864
+
+ propane-1,3-dithiol
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:46882
+ amino group
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:46883
+ carboxy group
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:47266
+ hydrogen bromide
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:47875
+ tetrabromomethane
+
+
+
+
+
+
+
+
+ Ethers ROR' where R has a double bond adjacent to the oxygen of the ether linkage.
+ http://purl.obolibrary.org/obo/chebi/205/chebi.owl
+ chebi_ontology
+ CHEBI:47985
+
+ enol ether
+
+
+
+
+
+
+
+
+ Enol ethers ROR' where R' has the structure SiR''R'''R''''.
+ http://purl.obolibrary.org/obo/chebi/205/chebi.owl
+ chebi_ontology
+ CHEBI:47986
+
+ silyl enol ether
+
+
+
+
+
+
+
+
+
+ Ethers ROR' where R' has the structure SiR''R'''R''''.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:47988
+
+ silyl ether
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:48420
+ chromium trioxide
+
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:48513
+ carbazoles
+
+
+
+
+
+
+
+
+
+ An azole in which the five-membered heterocyclic aromatic skeleton contains a N atom and one S atom.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:48901
+
+ thiazoles
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:49553
+ copper(II) chloride
+
+
+
+
+
+
+
+
+ A compound formally derived from ammonia by replacing one, two or three hydrogen atoms by organyl groups.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:50047
+
+ organic amino compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:50075
+ dihydropyridine
+
+
+
+
+
+
+
+
+ http://purl.obolibrary.org/obo/chebi/205/chebi.owl
+ CHEBI:24671
+ CHEBI:5798
+ chebi_ontology
+ CHEBI:50413
+
+ hydroxyaldehyde
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:50784
+ pivalate ester
+
+
+
+
+
+
+
+
+ A compound derived from an arene by replacing a hydrogen atom with a halogen atom.
+ http://purl.obolibrary.org/obo/chebi/200/chebi.owl
+ RXNO
+ chebi_ontology
+ CHEBI:50887
+
+ haloarene
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:50888
+ fluoroarene
+
+
+
+
+
+
+
+
+ A salt or ester of boronic acid.
+ http://purl.obolibrary.org/obo/chebi/200/chebi.owl
+ chebi_ontology
+ CHEBI:50978
+
+ boronate
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:51080
+ nitrate ester
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:51142
+ amino groups
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:51154
+ phosphonium ylide
+
+
+
+
+
+
+
+
+ A compound containing at least one carbon-lithium bond.
+ http://purl.obolibrary.org/obo/chebi/200/chebi.owl
+ chebi_ontology
+ CHEBI:51186
+
+ organolithium compound
+
+
+
+
+
+
+
+
+ A compound containing at least one carbon-magnesium bond.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:51187
+
+ organomagnesium compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:51236
+ organomagnesium halide
+
+
+
+
+
+
+
+
+ A compound of general formula RC(=O)SR'. Compare with thionoester, RC(=S)OR'.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:51277
+
+ thioester
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:51454
+ cyclopropanes
+
+
+
+
+
+
+
+
+ An organolithium compound where an alkyl group is bound to a lithium atom.
+ http://purl.obolibrary.org/obo/chebi/200/chebi.owl
+ chebi_ontology
+ CHEBI:51462
+
+ alkyllithium compound
+
+
+
+
+
+
+
+
+ An alkyllithium compound that has formula C4H9Li.
+ http://purl.obolibrary.org/obo/chebi/200/chebi.owl
+ chebi_ontology
+ CHEBI:51469
+
+ butyllithium
+
+
+
+
+
+
+
+
+ A compound containing at least one carbon-zinc bond.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:51494
+
+ organozinc compound
+
+
+
+
+
+
+
+
+ Any compound containing two aryl groups connected by a single C atom.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:51614
+
+ diarylmethane
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:51721
+ alpha,beta-unsaturated ketone
+
+
+
+
+
+
+
+
+
+ A haloketone in which the halogen and oxo substituents are on adjacent carbon atoms.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:51839
+
+ alpha-haloketone
+
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:51849
+ beta-ketoester
+
+
+
+
+
+
+
+
+ A ketone of formula RC(=O)CH3 (R =/= H).
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:51867
+
+ methyl ketone
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:51929
+ arylacetylene
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:52094
+ peroxy acid
+
+
+
+
+
+
+
+
+ A compound with the general formula R2C=O (R=/=H) where one or more of the R groups contains an oxy (-O-) group.
+ http://purl.obolibrary.org/obo/chebi/205/chebi.owl
+ chebi_ontology
+ CHEBI:52395
+
+ oxyketone
+
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:53212
+ isocyanates
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:53434
+ palladium(II) chloride
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:55380
+ beta-hydroxy ketone
+
+
+
+
+
+
+
+
+ A compound having the general formula RR'C(OH)OR'' (R'' =/= H).
+ 0
+ CH2O2R2
+ 46.025
+ 46.00548
+ Hemiacetal
+ hemiacetals
+ chebi_ontology
+ hemiacetals
+ CHEBI:5653
+
+ hemiacetal
+
+
+
+
+ Hemiacetal
+ KEGG_COMPOUND
+
+
+
+
+ hemiacetals
+ IUPAC
+
+
+
+
+
+ hemiacetals
+ ChEBI
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:5686
+ heterocyclic compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:59656
+ phosphine oxide
+
+
+
+
+
+
+
+
+ An organooxygen compound having the structure RR'C(OR'')(OR''') (R'', R''' =/= H). Mixed acetals have R'' and R''' groups which differ.
+ chebi_ontology
+ acetals
+ CHEBI:59769
+
+ acetal
+
+
+
+
+ acetals
+ ChEBI
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:59831
+ enyne
+
+
+
+
+
+
+
+
+ A chemical substance is a portion of matter of constant composition, composed of molecular entities of the same type or of different types.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:59999
+
+ chemical substance
+
+
+
+
+
+
+
+
+ A mixture is a chemical substance composed of multiple molecules, at least two of which are of a different kind.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:60004
+
+ mixture
+
+
+
+
+
+
+
+
+ A polymer is a mixture, which is composed of macromolecules of different kinds and which may be differentiated by composition, length, degree of branching etc..
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:60027
+
+ polymer
+
+
+
+
+
+
+
+
+ An organic phosphonate containing a C-PO(OH)2 or C-PO(OR)2 group (where R = alkyl group).
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ CHEBI:2591
+ chebi_ontology
+ CHEBI:60983
+
+ alkylphosphonate
+
+
+
+
+
+
+
+
+
+ An organic phosphonate of formula (RO)2P(=O)-CR2-NR2; R can be H.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:61111
+
+ aminophosphonate
+
+
+
+
+
+
+
+
+ Any monocyclic heteroarene consisting of a five-membered ring containing nitrogen. Azoles can also contain one or more other non-carbon atoms, such as nitrogen, sulfur or oxygen.
+ http://purl.obolibrary.org/obo/chebi/206/chebi.owl
+ chebi_ontology
+ CHEBI:68452
+
+ azole
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:72695
+ organic molecule
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:73474
+ acetylenic compound
+
+
+
+
+
+
+
+
+ RXNO
+ CHEBI:73477
+ terminal acetylenic compound
+
+
+
+
+
+
+
+
+ RXNO
+ IAO:0000005
+ objective specification
+
+
+
+
+
+
+
+ RXNO
+ IAO:0000030
+ information content entity
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an silyl group.
+ silylation
+ RXNO
+ MOP:0000339
+ has_participant: CHEBI:33478
+ silylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an silyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ RXNO
+ MOP:0000364
+ methylation
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an alkyl group.
+ alkylation
+ RXNO
+ MOP:0000369
+ has_participant: CHEBI:22323
+ alkylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an alkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a hydrocarbyl group.
+ hydrocarbylation
+ RXNO
+ MOP:0000410
+ has_participant: CHEBI:33248
+ hydrocarbylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a hydrocarbyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an aryl group.
+ arylation
+ RXNO
+ MOP:0000411
+ arylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an aryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an allyl group.
+ allylation
+ RXNO
+ MOP:0000422
+ has_participant: CHEBI:30361
+ allylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an allyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an organyl group.
+ organylation
+ RXNO
+ MOP:0000458
+ has_participant: CHEBI:33249
+ organylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an organyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an acyl group.
+ acylation
+ RXNO
+ MOP:0000479
+ has_participant: CHEBI:22221
+ acylation
+
+
+
+
+ Formation of a covalent bond between a substrate and an acyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfonyl group.
+ MOP:0000524
+ sulfonylation
+ RXNO
+ MOP:0000539
+ has_participant: CHEBI:51100; has_participant: CHEBI:29825
+ sulfonylation
+
+
+
+
+ Formation of a covalent bond between a substrate and a sulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A process in which at least one of the participants is a molecule.
+ RXNO
+ MOP:0000543
+ TODO: needs work, formal definition, etc.
+ molecular process
+
+
+
+
+ A process in which at least one of the participants is a molecule.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a halo group.
+ RXNO
+ MOP:0000550
+ has_participant: CHEBI:47854
+ halogenation
+
+
+
+
+ Formation of a covalent bond between a substrate and a halo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an imino group.
+ RXNO
+ MOP:0000555
+ has_participant: CHEBI:29342
+ imination
+
+
+
+
+ Formation of a covalent bond between a substrate and an imino group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a nitro group.
+ RXNO
+ MOP:0000556
+ nitration
+
+
+
+
+ Formation of a covalent bond between a substrate and a nitro group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a ring in a molecule from a chain by formation of a new bond.
+ cyclisation
+ RXNO
+ MOP:0000561
+ cyclization
+
+
+
+
+ Formation of a ring in a molecule from a chain by formation of a new bond.
+ AU:C01494
+
+
+
+
+
+
+
+
+ A molecular process where two or more unsaturated molecules or parts of the same molecule combine to form a cyclic adduct in which there is a net reduction of bond multiplicity.
+ RXNO:0000314
+ RXNO
+ MOP:0000562
+ cycloaddition
+
+
+
+
+ A molecular process where two or more unsaturated molecules or parts of the same molecule combine to form a cyclic adduct in which there is a net reduction of bond multiplicity.
+ AU:C01496
+
+
+
+
+
+
+
+
+ A cycloaddition in which each participant contributes two electrons to the transformation of reactants to products.
+ RXNO
+ MOP:0000563
+ [2+2] cycloaddition
+
+
+
+
+ A cycloaddition in which each participant contributes two electrons to the transformation of reactants to products.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A molecular process in which a cyclic system decomposes into two or more unsaturated molecules or parts of the same molecule and there is a net increase in bond multiplicity.
+ cycloreversion
+ retro-addition
+ retrocycloaddition
+ RXNO
+ MOP:0000564
+ cycloelimination
+
+
+
+
+ A molecular process in which a cyclic system decomposes into two or more unsaturated molecules or parts of the same molecule and there is a net increase in bond multiplicity.
+ AU:C01496
+ AU:C01501
+
+
+
+
+ cycloreversion
+ AU:C01506
+
+
+
+
+ retrocycloaddition
+ AU:R05372
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A cycloaddition in which one participant contributes four electrons and the other participant contributes two electrons to the transformation of reactants to products.
+ RXNO
+ MOP:0000565
+ [4+2] cycloaddition
+
+
+
+
+ A cycloaddition in which one participant contributes four electrons and the other participant contributes two electrons to the transformation of reactants to products.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a group.
+ batchelorc
+ 2009-04-22T10:01:32Z
+ RXNO
+ MOP:0000566
+ formation of covalent bond with group
+
+
+
+
+ Formation of a covalent bond between a substrate and a group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a group.
+ batchelorc
+ 2009-04-30T02:24:32Z
+ RXNO
+ MOP:0000567
+ breaking of covalent bond with group
+
+
+
+
+ Breaking of a covalent bond between a substrate and a group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ The complete, net removal of one or mole electrons from a molecular entity, corresponding to an increase in the oxidation number of any atom within any substrate.
+ batchelorc
+ 2009-06-01T06:01:47Z
+ de-electronation
+ RXNO
+ MOP:0000568
+ oxidation
+
+
+
+
+ The complete, net removal of one or mole electrons from a molecular entity, corresponding to an increase in the oxidation number of any atom within any substrate.
+ AU:O04362
+
+
+
+
+
+
+
+
+ The complete transfer of one or more electrons to a molecular entity.
+ batchelorc
+ 2009-06-01T06:04:18Z
+ electronation
+ RXNO
+ MOP:0000569
+ reduction
+
+
+
+
+ The complete transfer of one or more electrons to a molecular entity.
+ AU:R05222
+
+
+
+
+
+
+
+
+ The transfer of an electron to a molecular entity, resulting in a molecular entity of increased negative charge.
+ batchelorc
+ 2009-06-01T06:06:19Z
+ RXNO
+ MOP:0000570
+ electron attachment
+
+
+
+
+ The transfer of an electron to a molecular entity, resulting in a molecular entity of increased negative charge.
+ AU:E01979
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reduction in which an aldehyde is reduced to form a primary alcohol.
+ batchelorc
+ 2009-06-01T06:07:02Z
+ RXNO
+ MOP:0000571
+ aldehyde reduction
+
+
+
+
+ A reduction in which an aldehyde is reduced to form a primary alcohol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An oxidation process where an alcohol is transformed into a carbonyl compound.
+ batchelorc
+ 2009-06-01T06:10:35Z
+ RXNO
+ MOP:0000572
+ alcohol oxidation
+
+
+
+
+ An oxidation process where an alcohol is transformed into a carbonyl compound.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An oxidation process where a primary alcohol is transformed into an aldehyde.
+ batchelorc
+ 2009-06-01T06:10:59Z
+ RXNO
+ MOP:0000573
+ primary alcohol oxidation to aldehyde
+
+
+
+
+ An oxidation process where a primary alcohol is transformed into an aldehyde.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An oxidation process where a secondary alcohol is transformed into a ketone.
+ batchelorc
+ 2009-06-01T06:11:31Z
+ RXNO
+ MOP:0000574
+ secondary alcohol oxidation to ketone
+
+
+
+
+ An oxidation process where a secondary alcohol is transformed into a ketone.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An oxidation process where an amine is transformed into an imine.
+ batchelorc
+ 2009-06-01T06:15:40Z
+ RXNO
+ MOP:0000575
+ amine oxidation
+
+
+
+
+ An oxidation process where an amine is transformed into an imine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A reduction process where an imine is transformed into an amine.
+ batchelorc
+ 2009-06-01T06:19:21Z
+ RXNO
+ MOP:0000576
+ imine reduction
+
+
+
+
+ A reduction process where an imine is transformed into an amine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reduction process where the oxidation state carbonyl carbon in the ester functionality is reduced.
+ batchelorc
+ 2009-06-02T05:30:48Z
+ reduction of ester
+ RXNO
+ MOP:0000577
+ ester reduction
+
+
+
+
+ A reduction process where the oxidation state carbonyl carbon in the ester functionality is reduced.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An ester reduction where the product is the corresponding aldehyde.
+ batchelorc
+ 2009-06-02T05:31:49Z
+ reduction of ester to aldehyde
+ reduction of esters to aldehyde
+ RXNO
+ MOP:0000578
+ ester reduction to aldehyde
+
+
+
+
+ An ester reduction where the product is the corresponding aldehyde.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An ester reduction where the product is the corresponding primary alcohol.
+ batchelorc
+ 2009-06-02T05:32:37Z
+ reduction of ester to primary alcohol
+ reduction of esters to primary alcohol
+ RXNO
+ MOP:0000579
+ ester reduction to primary alcohol
+
+
+
+
+ An ester reduction where the product is the corresponding primary alcohol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reduction process where a ketone is reduced to a secondary alcohol.
+ batchelorc
+ 2009-06-02T05:35:42Z
+ reduction of ketone
+ reduction of ketones
+ RXNO
+ MOP:0000580
+ ketone reduction
+
+
+
+
+ A reduction process where a ketone is reduced to a secondary alcohol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An oxidation process where the oxidation state of at least one doubly-bonded carbon atom increases.
+ batchelorc
+ 2009-06-02T05:45:30Z
+ olefin oxidation
+ RXNO
+ MOP:0000581
+ alkene oxidation
+
+
+
+
+ An oxidation process where the oxidation state of at least one doubly-bonded carbon atom increases.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An alkene oxidation where the product is the corresponding 1,2-diol.
+ batchelorc
+ 2009-06-02T05:46:52Z
+ alkene oxidation to glycol
+ oxidation of alkene to 1,2-diol
+ oxidation of alkenes to 1,2-diol
+ RXNO
+ MOP:0000582
+ alkene oxidation to 1,2-diol
+
+
+
+
+ An alkene oxidation where the product is the corresponding 1,2-diol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An alkene oxidation where the reagent is ozone and the product is the corresponding ozonide.
+ batchelorc
+ 2009-06-02T05:48:42Z
+ ozonolysis of alkene
+ ozonolysis of alkenes
+ RXNO
+ MOP:0000583
+ alkene ozonolysis
+
+
+
+
+ An alkene oxidation where the reagent is ozone and the product is the corresponding ozonide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An alkene oxidation process where the reactant is a primary alkene and the products are carboxylic acid and carbon dioxide. This can be achieved with a warm, acidic solution of potassium permanganate.
+ batchelorc
+ 2009-06-02T06:02:46Z
+ RXNO
+ MOP:0000584
+ primary alkene oxidation to carboxylic acid and carbon dioxide
+
+
+
+
+ An alkene oxidation process where the reactant is a primary alkene and the products are carboxylic acid and carbon dioxide. This can be achieved with a warm, acidic solution of potassium permanganate.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An alkene oxidation where the reactant is a tertiary alkene and the products are the corresponding carboxylic acid and ketone. This can be achieved with a warm, acidic solution of potassium permanganate.
+ batchelorc
+ 2009-06-02T06:04:14Z
+ RXNO
+ MOP:0000585
+ tertiary alkene oxidation to carboxylic acid and ketone
+
+
+
+
+ An alkene oxidation where the reactant is a tertiary alkene and the products are the corresponding carboxylic acid and ketone. This can be achieved with a warm, acidic solution of potassium permanganate.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An alkene oxidation process where the reactant is a secondary alkene and the products are the corresponding aldehydes. This can be achieved with warm, acidic potassium permanganate.
+ batchelorc
+ 2009-06-02T06:06:23Z
+ RXNO
+ MOP:0000586
+ secondary, non-terminal alkene oxidation to aldehydes
+
+
+
+
+ An alkene oxidation process where the reactant is a secondary alkene and the products are the corresponding aldehydes. This can be achieved with warm, acidic potassium permanganate.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An alkene oxidation process where the reactant is a secondary terminal alkene and the products are carbon dioxide and the corresponding ketone. This can be achieved by warm, acidic potassium permanganate solution.
+ batchelorc
+ 2009-06-02T06:07:44Z
+ RXNO
+ MOP:0000587
+ secondary terminal alkene oxidation to ketone and carbon dioxide
+
+
+
+
+ An alkene oxidation process where the reactant is a secondary terminal alkene and the products are carbon dioxide and the corresponding ketone. This can be achieved by warm, acidic potassium permanganate solution.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An alkene oxidation process where the reactant is a quaternary alkene and the products are the corresponding ketones.
+ batchelorc
+ 2009-06-02T06:09:24Z
+ RXNO
+ MOP:0000588
+ quaternary alkene oxidation to ketones
+
+
+
+
+ An alkene oxidation process where the reactant is a quaternary alkene and the products are the corresponding ketones.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A reduction process that involves addition of hydrogen atoms across a double bond.
+ batchelorc
+ 2009-06-05T04:53:34Z
+ RXNO
+ MOP:0000589
+ hydrogenation
+
+
+
+
+ A reduction process that involves addition of hydrogen atoms across a double bond.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and a pseudohalo group.
+ RXNO
+ MOP:0000596
+ pseudohalogenation
+
+
+
+
+ Formation of a covalent bond between a substrate and a pseudohalo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A molecular process where a molecule is broken up by reaction with a molecule that is part of the solvent material. It may be the primary constituent molecule of the solvent material (for example water, ethanol, ammonia) or its lyonium ion or lyate ion.
+ batchelorc
+ 2009-09-16T11:11:24Z
+ RXNO
+ MOP:0000618
+ solvolysis
+
+
+
+
+ A molecular process where a molecule is broken up by reaction with a molecule that is part of the solvent material. It may be the primary constituent molecule of the solvent material (for example water, ethanol, ammonia) or its lyonium ion or lyate ion.
+ AU:S05762
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A solvolysis reaction where the solvent material is water.
+ batchelorc
+ 2009-09-16T11:13:21Z
+ RXNO
+ MOP:0000619
+ hydrolysis
+
+
+
+
+ A solvolysis reaction where the solvent material is water.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A reaction in which two or more reactants or remote reactive sites within the same molecular entity yield a single main product with accompanying formation of a small molecule.
+ batchelorc
+ 2009-09-16T11:30:32Z
+ RXNO:0000315
+ RXNO
+ MOP:0000627
+ condensation reaction
+
+
+
+
+ A reaction in which two or more reactants or remote reactive sites within the same molecular entity yield a single main product with accompanying formation of a small molecule.
+ AU:C01238
+
+
+
+
+
+
+
+
+ A condensation reaction where the small molecule produced is water.
+ batchelorc
+ 2009-09-16T11:32:33Z
+ RXNO
+ MOP:0000628
+ molecular dehydration reaction
+
+
+
+
+ A condensation reaction where the small molecule produced is water.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A reaction of two or more reacting molecular entities resulting in a single reaction product containing all atoms of all components with formation of two chemical bonds and a net reduction in bond multiplicity.
+ MOP:0000642
+ addition reaction
+
+
+
+
+ A reaction of two or more reacting molecular entities resulting in a single reaction product containing all atoms of all components with formation of two chemical bonds and a net reduction in bond multiplicity.
+ https://doi.org/10.1351/goldbook.A00133
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a substrate and an amino group.
+ RXNO
+ MOP:0000650
+ amination
+
+
+
+
+ Formation of a covalent bond between a substrate and an amino group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A molecular process where two groups are lost with concomitant formation of an unsaturation in the molecule or formation of a new ring.
+ RXNO
+ MOP:0000656
+ elimination reaction
+
+
+
+
+ A molecular process where two groups are lost with concomitant formation of an unsaturation in the molecule or formation of a new ring.
+ doi:10.1351/goldbook.E02038
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A cyclisation that results in the formation of an epoxide.
+ RXNO
+ MOP:0000671
+ epoxidation
+
+
+
+
+ A cyclisation that results in the formation of an epoxide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An oxidation process where the oxidation state of at least one sulfur atom increases.
+ RXNO
+ MOP:0000705
+ oxidation at sulfur
+
+
+
+
+ An oxidation process where the oxidation state of at least one sulfur atom increases.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An oxidation process where the oxidation state of at least one nitrogen atom increases.
+ RXNO
+ MOP:0000706
+ oxidation at nitrogen
+
+
+
+
+ An oxidation process where the oxidation state of at least one nitrogen atom increases.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A formal account of the degree of oxidation of an atom.
+ http://goldbook.iupac.org/O04365.html
+ RXNO
+ MOP:0000712
+ It turns out to be formally defined, which makes our definitions a bit poor.
+ oxidation state
+
+
+
+
+ A formal account of the degree of oxidation of an atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a molecule and a carboxy group.
+ RXNO
+ MOP:0000713
+ carboxylation
+
+
+
+
+ Formation of a covalent bond between a molecule and a carboxy group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Oxidation of a carbonyl group to an alkyne.
+ RXNO
+ MOP:0000714
+ carbonyl oxidation to alkyne
+
+
+
+
+ Oxidation of a carbonyl group to an alkyne.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A cycloaddition in which one participant contributes three electrons and the other participant contributes two electrons to the transformation of reactants to products.
+ RXNO
+ MOP:0000715
+ [3+2] cycloaddition
+
+
+
+
+ A cycloaddition in which one participant contributes three electrons and the other participant contributes two electrons to the transformation of reactants to products.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Molecular process in which an aldehyde or ketone tautomerises to form an enol.
+ enolization
+ RXNO
+ MOP:0000716
+ enolisation
+
+
+
+
+ Molecular process in which an aldehyde or ketone tautomerises to form an enol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Disposition that is realised in the process of enolisation
+ RXNO
+ MOP:0000717
+ enolisability
+
+
+
+
+ Disposition that is realised in the process of enolisation
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbonyl compound that bears the disposition to be enolised.
+ RXNO
+ MOP:0000718
+ this surely belongs in ChEBI but put it here pro tem
+ enolisable carbonyl compound
+
+
+
+
+ A carbonyl compound that bears the disposition to be enolised.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between an alkyl group and an oxygen atom.
+ RXNO
+ MOP:0000719
+ O-dealkylation
+
+
+
+
+ Breaking of a covalent bond between an alkyl group and an oxygen atom.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A cycloaddition in which two participants contribute two electrons and the other participant contributes one electron to the transformation of reactants to products.
+ RXNO
+ MOP:0000720
+ [2+2+1] cycloaddition
+
+
+
+
+ A cycloaddition in which two participants contribute two electrons and the other participant contributes one electron to the transformation of reactants to products.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ RXNO:0000027
+ RXNO
+ MOP:0000721
+ This term was obsoleted from the RXNO namespace and transferred to MOP because it is a process identifiable by its mechanism rather than the intention of the experimenter.
+ [3,3]-sigmatropic rearrangement
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which two or more reactants or remote reactive sites within the same molecular entity yield a single main product with accompanying formation of a carbon dioxide molecule.
+ batchelorc
+ 2014-03-05T10:00:00Z
+ RXNO
+ MOP:0000722
+ decarboxylative condensation
+
+
+
+
+ A reaction in which two or more reactants or remote reactive sites within the same molecular entity yield a single main product with accompanying formation of a carbon dioxide molecule.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A reaction in which two or more reactants or remote reactive sites within the same molecular entity yield a single main product with accompanying formation of an ethanol molecule.
+ batchelorc
+ 2014-03-05T10:00:00Z
+ RXNO
+ MOP:0000723
+ deethanolative condensation
+
+
+
+
+ A reaction in which two or more reactants or remote reactive sites within the same molecular entity yield a single main product with accompanying formation of an ethanol molecule.
+ RSC:xp
+
+
+
+
+
+
+
+
+ batchelorc
+ 2014-04-09T10:00:00Z
+ RXNO
+ MOP:0000730
+ Brønsted acid catalysis
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ batchelorc
+ 2014-04-09T10:00:00Z
+ RXNO
+ MOP:0000731
+ base catalysis
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ batchelorc
+ 2014-04-09T10:00:00Z
+ RXNO
+ MOP:0000732
+ hydron donation
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ batchelorc
+ 2014-04-09T10:00:00Z
+ RXNO
+ MOP:0000733
+ accepting an electron pair in Lewis adduct formation
+
+
+
+
+
+
+
+
+ batchelorc
+ 2014-04-09T10:00:00Z
+ RXNO
+ MOP:0000734
+ Lewis acid catalysis
+
+
+
+
+
+
+
+
+ batchelorc
+ 2014-04-09T10:00:00Z
+ RXNO
+ MOP:0000735
+ Lewis base catalysis
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ batchelorc
+ 2014-04-09T10:00:00Z
+ RXNO
+ MOP:0000736
+ Brønsted base catalysis
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ batchelorc
+ 2014-04-09T10:00:00Z
+ RXNO
+ MOP:0000737
+ accepting a hydron
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ batchelorc
+ 2014-04-09T10:00:00Z
+ RXNO
+ MOP:0000738
+ electron pair donation in Lewis adduct formation
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ RXNO
+ MOP:0000739
+ Lewis adduct formation
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Catalysis of a reaction where the catalyst either donates a hydron or accepts an electron pair.
+ RXNO
+ MOP:0000740
+ acid catalysis
+
+
+
+
+ Catalysis of a reaction where the catalyst either donates a hydron or accepts an electron pair.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A reaction in which one singly-bonded group, but not the hydrogen atom, is replaced by another singly-bonded group.
+ RXNO:0000019
+ RXNO
+ MOP:0000790
+ The Gold Book says hydrogen atoms count, but this differs from everyone's intuition. See http://goldbook.iupac.org/S06078.html
+ substitution reaction
+
+
+
+
+ A reaction in which one singly-bonded group, but not the hydrogen atom, is replaced by another singly-bonded group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A substitution reaction in which one singly-bonded substituent on an aromatic skeleton is replaced by another singly-bonded substituent.
+ RXNO:0000020
+ RXNO
+ MOP:0000791
+ aromatic substitution
+
+
+
+
+ A substitution reaction in which one singly-bonded substituent on an aromatic skeleton is replaced by another singly-bonded substituent.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A substitution reaction in an allylic system with concomitant migration of the allyl double bond.
+ RXNO:0000033
+ RXNO
+ MOP:0000792
+ allylic rearrangement
+
+
+
+
+ A substitution reaction in an allylic system with concomitant migration of the allyl double bond.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A substitution reaction where the reactive centre is a nitrogen atom.
+ RXNO:0000319
+ RXNO
+ MOP:0000793
+ N-substitution
+
+
+
+
+ A substitution reaction where the reactive centre is a nitrogen atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A substitution reaction where the reactive centre is an oxygen atom.
+ RXNO:0000318
+ NAMERXN:1.7
+ RXNO
+ MOP:0000794
+ O-substitution
+
+
+
+
+ A substitution reaction where the reactive centre is an oxygen atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A substitution reaction where the reactive centre is a sulfur atom.
+ batchelorc
+ 2012-03-22T12:22:59Z
+ RXNO:0000336
+ NAMERXN:1.8
+ RXNO
+ MOP:0000795
+ S-substitution
+
+
+
+
+ A substitution reaction where the reactive centre is a sulfur atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a nitrogen centre.
+ RXNO
+ MOP:0000802
+ formation of covalent bond with nitrogen centre
+
+
+
+
+ Formation of a covalent bond with a group where the free valence is on a nitrogen centre.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A reaction in which two or more reactants or remote reactive sites within the same molecular entity yield a single main product with accompanying formation of an alcohol molecule.
+ RXNO
+ MOP:0000825
+ dealcoholative condensation
+
+
+
+
+ A reaction in which two or more reactants or remote reactive sites within the same molecular entity yield a single main product with accompanying formation of an alcohol molecule.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A disposition which is realised in a [4+2] reaction with a double-bonded system.
+ http://goldbook.iupac.org/D01700.html
+ RXNO
+ MOP:0000826
+ dienophilicity
+
+
+
+
+ A disposition which is realised in a [4+2] reaction with a double-bonded system.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between an alkyl group and a substrate.
+ RXNO
+ MOP:0001369
+ dealkylation
+
+
+
+
+ Breaking of a covalent bond between an alkyl group and a substrate.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and an organyl group.
+ RXNO
+ MOP:0001458
+ has_participant: CHEBI:33249
+ deorganylation
+
+
+
+
+ Breaking of a covalent bond between a substrate and an organyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a substrate and a halo group.
+ RXNO
+ MOP:0001550
+ has_participant: CHEBI:47854
+ dehalogenation
+
+
+
+
+ Breaking of a covalent bond between a substrate and a halo group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Breaking of a covalent bond between a molecule and a carboxy group.
+ RXNO
+ MOP:0001713
+ decarboxylation
+
+
+
+
+ Breaking of a covalent bond between a molecule and a carboxy group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a methyl group.
+ RXNO
+ MOP:0002364
+ has_participant: CHEBI:32875
+ N-methylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a methyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alkyl group.
+ RXNO
+ MOP:0002369
+ has_participant: CHEBI:22323
+ N-alkylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an alkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an aryl group.
+ RXNO
+ MOP:0002411
+ N-arylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an aryl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acyl group.
+ RXNO
+ MOP:0002479
+ has_participant: CHEBI:22221
+ N-acylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and an acyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfonyl group.
+ RXNO
+ MOP:0002524
+ has_participant: CHEBI:29825
+ N-sulfonylation
+
+
+
+
+ Formation of a covalent bond between a nitrogen atom in a substrate and a sulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a silyl group.
+ RXNO
+ MOP:0003339
+ has_participant: CHEBI:30541
+ O-silylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a silyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acyl group.
+ RXNO
+ MOP:0003479
+ has_participant: CHEBI:22221
+ O-acylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and an acyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfonyl group.
+ RXNO
+ MOP:0003524
+ has_participant: CHEBI:29825
+ O-sulfonylation
+
+
+
+
+ Formation of a covalent bond between an oxygen atom in a substrate and a sulfonyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ The formation of a covalent bond between a phosphorus atom and an alkyl group.
+ RXNO
+ MOP:0006369
+ P-alkylation
+
+
+
+
+ The formation of a covalent bond between a phosphorus atom and an alkyl group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ RXNO
+ OBI:0000011
+ planned process
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction where the number of atoms in the molecular skeleton increases.
+ coupling reaction
+ RXNO
+ RXNO:0000000
+ molecular skeleton joining reaction
+
+
+
+
+ A reaction where the number of atoms in the molecular skeleton increases.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A molecular process with which the experimenters aim to achieve a particular molecular transformation.
+ RXNO
+ RXNO:0000001
+ planned reaction step
+
+
+
+
+ A molecular process with which the experimenters aim to achieve a particular molecular transformation.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A reaction where a bond is formed between two carbon atoms.
+ NAMERXN:3
+ RXNO
+ RXNO:0000002
+ carbon-carbon coupling reaction
+
+
+
+
+ A reaction where a bond is formed between two carbon atoms.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An aldol condensation where an aryl aldehyde reacts with an acid anhydride to form a cinnamic acid.
+ https://www.rsc.org/Merck-Index/reaction/r327/
+ https://www.wikidata.org/wiki/Q898605
+ RXNO
+ RXNO:0000003
+ Perkin reaction
+
+
+
+
+ An aldol condensation where an aryl aldehyde reacts with an acid anhydride to form a cinnamic acid.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+ A reaction in which the number of atoms in any ring changes between the reactant and the products.
+ RXNO
+ RXNO:0000004
+ This term was obsoleted because it was a grouping term that wasn't much help.
+ obsolete: ring reaction
+ true
+
+
+
+
+ A reaction in which the number of atoms in any ring changes between the reactant and the products.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A planned reaction step where the product contains a ring that was not in any of the reactants.
+ RXNO
+ RXNO:0000005
+ ring formation reaction step
+
+
+
+
+ A planned reaction step where the product contains a ring that was not in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A [4+2] cycloaddition reaction where a diene reacts with a compound containing a double or triple bond (a dienophile) to form an unsaturated six-membered ring compound.
+ NAMERXN:3.11.3
+ https://www.rsc.org/Merck-Index/reaction/r109/
+ https://www.wikidata.org/wiki/Q375669
+ Diels-Alder coupling
+ Diels-Alder cycloaddition
+ RXNO
+ RXNO:0000006
+ Diels-Alder reaction
+
+
+
+
+ A [4+2] cycloaddition reaction where a diene reacts with a compound containing a double or triple bond (a dienophile) to form an unsaturated six-membered ring compound.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A joining reaction where an alkene with an allylic hydrogen reacts with a compound containing a multiple bond (an enophile) to form a substituted alkene.
+ https://www.rsc.org/Merck-Index/reaction/r129/
+ https://www.wikidata.org/wiki/Q26469
+ RXNO
+ RXNO:0000007
+ ene reaction
+
+
+
+
+ A joining reaction where an alkene with an allylic hydrogen reacts with a compound containing a multiple bond (an enophile) to form a substituted alkene.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A joining reaction where a nucleophile adds to the beta-carbon of an alpha,beta-unsaturated system (or an activated carbon-carbon bond).
+ https://www.wikidata.org/wiki/Q2181524
+ nucleophilic conjugate addition
+ RXNO
+ RXNO:0000008
+ conjugate addition
+
+
+
+
+ A joining reaction where a nucleophile adds to the beta-carbon of an alpha,beta-unsaturated system (or an activated carbon-carbon bond).
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+ A conjugate addition reaction where a carbon nucleophile adds to the beta-carbon of an alpha,beta-unsaturated system (or an activated carbon-carbon bond).
+ https://www.rsc.org/Merck-Index/reaction/r281/
+ https://www.wikidata.org/wiki/Q642233
+ Michael reaction
+ RXNO
+ RXNO:0000009
+ Michael addition
+
+
+
+
+ A conjugate addition reaction where a carbon nucleophile adds to the beta-carbon of an alpha,beta-unsaturated system (or an activated carbon-carbon bond).
+ RSC:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction where the number of atoms in the skeleton, and their connectivity, remain the same.
+ RXNO
+ RXNO:0000010
+ functional modification
+
+
+
+
+ A reaction where the number of atoms in the skeleton, and their connectivity, remain the same.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which a functional group undergoes a change that does not affect the number of atoms in (or connectivity of) the skeleton of the molecule.
+ NAMERXN:9
+ RXNO
+ RXNO:0000011
+ functional group modification
+
+
+
+
+ A reaction in which a functional group undergoes a change that does not affect the number of atoms in (or connectivity of) the skeleton of the molecule.
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A functional group modification reaction where a functional group is oxidised.
+ RXNO
+ RXNO:0000012
+ functional group oxidation
+
+
+
+
+ A functional group modification reaction where a functional group is oxidised.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A functional group oxidation where an aromatic amine is transformed into an aromatic diazonium salt.
+ diazotization
+ RXNO
+ RXNO:0000013
+ diazotisation
+
+
+
+
+ A functional group oxidation where an aromatic amine is transformed into an aromatic diazonium salt.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction where a Grignard reagent reacts with a compound containing an electrophilic carbon atom. A Grignard reagent is a magnesium-stabilised carbon nucleophile. An aldehyde leads to a secondary alcohol, a ketone leads to a tertiary alcohol, an ester leads to a ketone and a nitrile leads to a ketone.
+ NAMERXN:3.7
+ https://www.rsc.org/Merck-Index/reaction/r177/
+ https://www.wikidata.org/wiki/Q337748
+ RXNO
+ RXNO:0000014
+ Grignard reaction
+
+
+
+
+ A carbon-carbon coupling reaction where a Grignard reagent reacts with a compound containing an electrophilic carbon atom. A Grignard reagent is a magnesium-stabilised carbon nucleophile. An aldehyde leads to a secondary alcohol, a ketone leads to a tertiary alcohol, an ester leads to a ketone and a nitrile leads to a ketone.
+ RSC:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction where a carbonyl compound reacts with a phosphonium ylide to give an alkene.
+ NAMERXN:3.8
+ https://www.rsc.org/Merck-Index/reaction/r468/
+ https://www.wikidata.org/wiki/Q909735
+ Wittig condensation
+ Wittig olefination
+ RXNO
+ RXNO:0000015
+ Wittig reaction
+
+
+
+
+ A carbon-carbon coupling reaction where a carbonyl compound reacts with a phosphonium ylide to give an alkene.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction where an enol or enolate reacts with a carbonyl compound to form a beta-hydroxy ketone. The name comes from aldehyde + alcohol.
+ https://www.rsc.org/Merck-Index/reaction/r4/
+ https://www.wikidata.org/wiki/Q494392
+ aldol reaction
+ RXNO
+ RXNO:0000016
+ aldol addition
+
+
+
+
+ A carbon-carbon coupling reaction where an enol or enolate reacts with a carbonyl compound to form a beta-hydroxy ketone. The name comes from aldehyde + alcohol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An aldol addition where an enol or enolate reacts with a carbonyl compound to form an alpha,beta-unsaturated ketone.
+ https://www.rsc.org/Merck-Index/reaction/r4/
+ https://www.wikidata.org/wiki/Q1027170
+ RXNO
+ RXNO:0000017
+ aldol condensation
+
+
+
+
+ An aldol addition where an enol or enolate reacts with a carbonyl compound to form an alpha,beta-unsaturated ketone.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A ring formation reaction where a 1,3-dipolar compound reacts with an alkene or alkyne to form a five-membered ring compound.
+ https://www.wikidata.org/wiki/Q902907
+ Huisgen cycloaddition
+ Huisgen reaction
+ Huisgen's 1,3-dipolar cycloaddition
+ RXNO
+ RXNO:0000018
+ 1,3-dipolar cycloaddition
+
+
+
+
+ A ring formation reaction where a 1,3-dipolar compound reacts with an alkene or alkyne to form a five-membered ring compound.
+ RSC:db
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with a copper(I) halide or pseudohalide to form an aromatic halide or pseudohalide.
+ https://www.rsc.org/Merck-Index/reaction/r386/
+ https://www.wikidata.org/wiki/Q898821
+ RXNO
+ RXNO:0000021
+ Sandmeyer reaction
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with a copper(I) halide or pseudohalide to form an aromatic halide or pseudohalide.
+ RSC:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with copper powder and hydrochloric acid or hydrobromic acid to form an aromatic chloride or bromide.
+ RXNO
+ Gattermann reaction
+ RXNO:0000022
+ This is also sometimes known as the Gattermann reaction. Also doesn't work to make fluorides or iodides.
+ Gattermann halogenation
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with copper powder and hydrochloric acid or hydrobromic acid to form an aromatic chloride or bromide.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with a copper(II) halide to form an aromatic halide.
+ RXNO
+ RXNO:0000023
+ Koerner-Contardi reaction
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with a copper(II) halide to form an aromatic halide.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction where an organohalide or triflate couples to a terminal olefin to produce an internal olefin, catalysed by palladium. It is stereospecific.
+ NAMERXN:3.2
+ https://www.rsc.org/Merck-Index/reaction/r192/
+ https://www.wikidata.org/wiki/Q899916
+ Heck-Mizoroki reaction
+ Mizoroki-Heck reaction
+ RXNO
+ RXNO:0000024
+ This usually produces the trans-olefin rather than the cis-. ALSO Merck Index gives a non-terminal example.
+ Heck reaction
+
+
+
+
+ A carbon-carbon coupling reaction where an organohalide or triflate couples to a terminal olefin to produce an internal olefin, catalysed by palladium. It is stereospecific.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction which preserves the number of rings and number of skeletal atoms and in which the molecule rearranges so that one or more atoms or groups of atoms move from one atom to another.
+ RXNO
+ RXNO:0000025
+ rearrangement step
+
+
+
+
+ A reaction which preserves the number of rings and number of skeletal atoms and in which the molecule rearranges so that one or more atoms or groups of atoms move from one atom to another.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A rearrangement where an oxime rearranges to form an amide. Often there is selective migration of one group.
+ https://www.rsc.org/Merck-Index/reaction/r29/
+ https://www.wikidata.org/wiki/Q813746
+ RXNO
+ RXNO:0000026
+ Beckmann rearrangement
+
+
+
+
+ A rearrangement where an oxime rearranges to form an amide. Often there is selective migration of one group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+ A [3,3]-sigmatropic rearrangement where a 1,5-hexadiene rearranges to form a 1,5-hexadiene.
+ https://www.rsc.org/Merck-Index/reaction/r86/
+ https://www.wikidata.org/wiki/Q905087
+ RXNO
+ RXNO:0000028
+ Cope rearrangement
+
+
+
+
+ A [3,3]-sigmatropic rearrangement where a 1,5-hexadiene rearranges to form a 1,5-hexadiene.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ A [3,3]-sigmatropic rearrangement of a 3-hydroxy-1,5-hexadiene rearranges to form a 5,6-unsaturated carbonyl compound.
+ https://www.rsc.org/Merck-Index/reaction/r86/
+ https://www.wikidata.org/wiki/Q25326942
+ RXNO
+ RXNO:0000029
+ oxy-Cope rearrangement
+
+
+
+
+ A [3,3]-sigmatropic rearrangement of a 3-hydroxy-1,5-hexadiene rearranges to form a 5,6-unsaturated carbonyl compound.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A joining reaction in which one or more atoms are added to the middle of a chain.
+ RXNO
+ RXNO:0000030
+ molecular skeleton insertion reaction
+
+
+
+
+ A joining reaction in which one or more atoms are added to the middle of a chain.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction of a ketone to give an ester, in which an alkyl, benzyl or phenyl group migrates from one of the alpha-carbon centres to an adjacent oxygen, displacing an oxygen-based leaving group; the result is a formal insertion of an oxygen atom. The reaction also works with aldehydes, giving the corresponding carboxylic acid. The term "Baeyer-Villiger rearrangement" may occasionally be used in a mechanistic sense to refer specificially to the actual rearrangement step.
+ RXNO:0000190
+ https://www.rsc.org/Merck-Index/reaction/r13/
+ https://www.wikidata.org/wiki/Q182033
+ B-V reaction
+ Baeyer-Villiger oxidative rearrangement
+ Baeyer-Villiger reaction
+ RXNO
+ Baeyer-Villiger rearrangement
+ RXNO:0000031
+ Baeyer-Villiger oxidation
+
+
+
+
+ A reaction of a ketone to give an ester, in which an alkyl, benzyl or phenyl group migrates from one of the alpha-carbon centres to an adjacent oxygen, displacing an oxygen-based leaving group; the result is a formal insertion of an oxygen atom. The reaction also works with aldehydes, giving the corresponding carboxylic acid. The term "Baeyer-Villiger rearrangement" may occasionally be used in a mechanistic sense to refer specificially to the actual rearrangement step.
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction where ammonia or an amine reacts with a non-enolisable aldehyde, often methanal, and an enolisable carbonyl compound to form a beta-amino carbonyl compound.
+ https://www.rsc.org/Merck-Index/reaction/r265/
+ https://www.wikidata.org/wiki/Q183055
+ RXNO
+ RXNO:0000032
+ Mannich reaction
+
+
+
+
+ A carbon-carbon coupling reaction where ammonia or an amine reacts with a non-enolisable aldehyde, often methanal, and an enolisable carbonyl compound to form a beta-amino carbonyl compound.
+ RSC:db
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A substitution where an alcohol is converted into something else. Typical reagents are a dialkyl azodicarboxylate and a triarylphosphine. The alcohol stereocentre is inverted.
+ https://www.rsc.org/Merck-Index/reaction/r287/
+ https://www.wikidata.org/wiki/Q899062
+ RXNO
+ RXNO:0000034
+ Mitsunobu reaction
+
+
+
+
+ A substitution where an alcohol is converted into something else. Typical reagents are a dialkyl azodicarboxylate and a triarylphosphine. The alcohol stereocentre is inverted.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction where a stannane reacts with an organohalide or organotriflate.
+ NAMERXN:3.4
+ https://www.rsc.org/Merck-Index/reaction/r415/
+ https://www.wikidata.org/wiki/Q899861
+ Stille reaction
+ RXNO
+ RXNO:0000035
+ Stille coupling
+
+
+
+
+ A carbon-carbon coupling reaction where a stannane reacts with an organohalide or organotriflate.
+ RSC:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction where an aldehyde or amine reacts with a alpha-halo ester and zinc to form a beta-hydroxy ester.
+ https://www.rsc.org/Merck-Index/reaction/r361/
+ https://www.wikidata.org/wiki/Q898948
+ Reformatskii reaction
+ RXNO
+ RXNO:0000036
+ Reformatsky reaction
+
+
+
+
+ A carbon-carbon coupling reaction where an aldehyde or amine reacts with a alpha-halo ester and zinc to form a beta-hydroxy ester.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A functional group modification reaction where a functional group is reduced.
+ RXNO
+ RXNO:0000037
+ functional group reduction
+
+
+
+
+ A functional group modification reaction where a functional group is reduced.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A functional group reduction where an aldehyde or ketone carbonyl group is reduced to a methylene with zinc-mercury amalgam and hydrochloric acid.
+ https://www.rsc.org/Merck-Index/reaction/r82/
+ https://www.wikidata.org/wiki/Q898480
+ RXNO
+ RXNO:0000038
+ Clemmensen reduction
+
+
+
+
+ A functional group reduction where an aldehyde or ketone carbonyl group is reduced to a methylene with zinc-mercury amalgam and hydrochloric acid.
+ RSC:db
+
+
+
+
+
+
+
+
+ A joining reaction where a carbon-carbon bond is formed between like moieties.
+ RXNO
+ RXNO:0000039
+ carbon-carbon homocoupling reaction
+
+
+
+
+ A joining reaction where a carbon-carbon bond is formed between like moieties.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A carbon-carbon homocoupling reaction of an aryl halide mediated by copper.
+ https://www.rsc.org/Merck-Index/reaction/r441/
+ https://www.wikidata.org/wiki/Q904703
+ RXNO
+ RXNO:0000040
+ Ullmann reaction
+
+
+
+
+ A carbon-carbon homocoupling reaction of an aryl halide mediated by copper.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which two or more groups of atoms are added to the molecule, resulting in a change of skeletal bond order.
+ RXNO
+ RXNO:0000041
+ addition reaction step
+
+
+
+
+ A reaction in which two or more groups of atoms are added to the molecule, resulting in a change of skeletal bond order.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Addition of hydrogen atoms to aromatic rings by means of alkali metals in liquid ammonia.
+ https://www.rsc.org/Merck-Index/reaction/r44/
+ https://www.wikidata.org/wiki/Q864996
+ RXNO
+ RXNO:0000042
+ Birch reduction
+
+
+
+
+ Addition of hydrogen atoms to aromatic rings by means of alkali metals in liquid ammonia.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction of an ester and a carbonyl compound to form a beta-keto ester.
+ https://www.rsc.org/Merck-Index/reaction/r79/
+ https://www.wikidata.org/wiki/Q898501
+ RXNO
+ RXNO:0000043
+ Claisen condensation
+
+
+
+
+ A carbon-carbon coupling reaction of an ester and a carbonyl compound to form a beta-keto ester.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction of an aldehyde and a methylene compound.
+ https://www.rsc.org/Merck-Index/reaction/r230/
+ https://www.wikidata.org/wiki/Q898972
+ RXNO
+ RXNO:0000044
+ Knoevenagel condensation
+
+
+
+
+ A carbon-carbon coupling reaction of an aldehyde and a methylene compound.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction between an arene and a carbonyl compound (usually an acyl halide) to give an aryl ketone. The reaction is catalysed by a Lewis acid.
+ https://www.rsc.org/Merck-Index/reaction/r158/
+ https://www.wikidata.org/wiki/Q15130933
+ RXNO
+ RXNO:0000045
+ Friedel-Crafts acylation
+
+
+
+
+ A carbon-carbon coupling reaction between an arene and a carbonyl compound (usually an acyl halide) to give an aryl ketone. The reaction is catalysed by a Lewis acid.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction between an arene and an alkyl halide/alkene/alcohol (anything that can form a carbocation) to give a substituted arene. The reaction is catalysed by a Lewis acid.
+ https://www.rsc.org/Merck-Index/reaction/r158/
+ RXNO
+ RXNO:0000046
+ It proceeds by an SN1 mechanism.
+ Friedel-Crafts alkylation
+
+
+
+
+ A carbon-carbon coupling reaction between an arene and an alkyl halide/alkene/alcohol (anything that can form a carbocation) to give a substituted arene. The reaction is catalysed by a Lewis acid.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An oxidation of a secondary alcohol to a ketone involving an equilibrium between the alcohol and a reagent ketone present in excess, catalysed by a metal alkoxide.
+ https://www.rsc.org/Merck-Index/reaction/r311/
+ https://www.wikidata.org/wiki/Q902263
+ RXNO
+ RXNO:0000047
+ Oppenauer oxidation
+
+
+
+
+ An oxidation of a secondary alcohol to a ketone involving an equilibrium between the alcohol and a reagent ketone present in excess, catalysed by a metal alkoxide.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling between formaldehyde and an alkene to give a 1,3-diol or an allylic alcohol, catalysed by acid.
+ https://www.rsc.org/Merck-Index/reaction/r352/
+ https://www.wikidata.org/wiki/Q267374
+ RXNO
+ RXNO:0000048
+ See also "intramolecular Prins reaction".
+ Prins reaction
+
+
+
+
+ A carbon-carbon coupling between formaldehyde and an alkene to give a 1,3-diol or an allylic alcohol, catalysed by acid.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction between formaldehyde and an alkene to give a 1,3-dioxane, catalysed by acid.
+ https://www.rsc.org/Merck-Index/reaction/r352/
+ RXNO
+ RXNO:0000049
+ intramolecular Prins reaction
+
+
+
+
+ A reaction between formaldehyde and an alkene to give a 1,3-dioxane, catalysed by acid.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A rearrangement of a 1,2-diol to give a carbonyl compound, catalysed by acid.
+ https://www.rsc.org/Merck-Index/reaction/r341/
+ https://www.wikidata.org/wiki/Q902209
+ RXNO
+ RXNO:0000050
+ pinacol rearrangement
+
+
+
+
+ A rearrangement of a 1,2-diol to give a carbonyl compound, catalysed by acid.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A rearrangement of a diazoketone to give a ketene, with the elimination of molecular nitrogen.
+ https://www.rsc.org/Merck-Index/reaction/r474/
+ https://www.wikidata.org/wiki/Q255452
+ RXNO
+ RXNO:0000051
+ Wolff rearrangement
+
+
+
+
+ A rearrangement of a diazoketone to give a ketene, with the elimination of molecular nitrogen.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which a fused ring system is present in a product that was not present in any of the reactants.
+ RXNO
+ RXNO:0000052
+ fused-ring-system formation
+
+
+
+
+ A reaction in which a fused ring system is present in a product that was not present in any of the reactants.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A cyclodehydration of a beta-phenethylamide to give a 3,4-dihydroisoquinoline.
+ https://www.rsc.org/Merck-Index/reaction/r46/
+ https://www.wikidata.org/wiki/Q866098
+ Bischler-Napieralski 3,4-dihydroisoquinoline synthesis
+ Bischler-Napieralski dihydroisoquinoline synthesis
+ Bischler-Napieralski isoquinoline synthesis
+ RXNO
+ RXNO:0000053
+ Bischler-Napieralski reaction
+
+
+
+
+ A cyclodehydration of a beta-phenethylamide to give a 3,4-dihydroisoquinoline.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A rearrangement of an acyl azide to give an isocyanate by pyrolysis, with the elimination of molecular nitrogen.
+ https://www.rsc.org/Merck-Index/reaction/r97/
+ https://www.wikidata.org/wiki/Q254370
+ Curtius degradation
+ Curtius reaction
+ RXNO
+ RXNO:0000054
+ Curtius rearrangement
+
+
+
+
+ A rearrangement of an acyl azide to give an isocyanate by pyrolysis, with the elimination of molecular nitrogen.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A formylation of an activated arene with a disubstituted formamide to give an arenecarbaldehyde.
+ https://www.rsc.org/Merck-Index/reaction/r444/
+ https://www.wikidata.org/wiki/Q903038
+ Vilsmeier-Haack formylation
+ RXNO
+ RXNO:0000055
+ Vilsmeier-Haack reaction
+
+
+
+
+ A formylation of an activated arene with a disubstituted formamide to give an arenecarbaldehyde.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction between a phosphonate and a carbonyl compound to give an olefin.
+ https://www.rsc.org/Merck-Index/reaction/r468/
+ https://www.wikidata.org/wiki/Q905020
+ Emmons reaction
+ Horner-Emmons reaction
+ Horner-Emmons-Wadsworth reaction
+ Horner-Wadsworth-Emmons (HWE) olefination
+ Horner-Wadsworth-Emmons olefination
+ Horner-Wittig reaction
+ Wadsworth-Emmons olefination
+ Wadsworth-Emmons reaction
+ Wadsworth-Emmons-Horner reaction
+ Wittig-Horner reaction
+ RXNO
+ RXNO:0000056
+ Horner-Wadsworth-Emmons reaction
+
+
+
+
+ A carbon-carbon coupling reaction between a phosphonate and a carbonyl compound to give an olefin.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A joining reaction between a phosphine oxide and a carbonyl compound to give an olefin.
+ https://www.rsc.org/Merck-Index/reaction/r468/
+ RXNO
+ RXNO:0000057
+ Horner reaction
+
+
+
+
+ A joining reaction between a phosphine oxide and a carbonyl compound to give an olefin.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction between an alcohol or alkene and a nitrile to give an amide, catalysed by a Bronsted acid.
+ https://www.rsc.org/Merck-Index/reaction/r372/
+ https://www.wikidata.org/wiki/Q902273
+ RXNO
+ RXNO:0000058
+ Proceeds by an SN1 mechanism.
+ Ritter reaction
+
+
+
+
+ A reaction between an alcohol or alkene and a nitrile to give an amide, catalysed by a Bronsted acid.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A condensation-cyclisation of a beta-phenethylamine with an aldehyde to give a tetrahydroisoquinoline.
+ https://www.rsc.org/Merck-Index/reaction/r338/
+ https://www.wikidata.org/wiki/Q899206
+ Pictet-Spengler isoquinoline synthesis
+ Pictet-Spengler tetrahydroisoquinoline synthesis
+ RXNO
+ RXNO:0000059
+ Pictet-Spengler reaction
+
+
+
+
+ A condensation-cyclisation of a beta-phenethylamine with an aldehyde to give a tetrahydroisoquinoline.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The alkylation of a trialkyl phosphite with an alkyl halide or acyl halide to give an alkyl phosphonate.
+ RXNO:0000112
+ https://www.wikidata.org/wiki/Q630801
+ Michaelis-Arbuzov phosphonate synthesis
+ Michaelis-Arbuzov reaction
+ RXNO
+ RXNO:0000060
+ Arbuzov reaction
+
+
+
+
+ The alkylation of a trialkyl phosphite with an alkyl halide or acyl halide to give an alkyl phosphonate.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ An aldol condensation between an aldehyde or ketone and a silyl enol ether (also known as a ketene silyl acetal) to give a beta-hydroxy carbonyl compound.
+ https://www.wikidata.org/wiki/Q1059787
+ Mukaiyama aldol addition
+ Mukaiyama aldol reaction
+ RXNO
+ RXNO:0000061
+ Mukaiyama aldol condensation
+
+
+
+
+ An aldol condensation between an aldehyde or ketone and a silyl enol ether (also known as a ketene silyl acetal) to give a beta-hydroxy carbonyl compound.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A condensation between an aromatic amine and glycerol to give a quinoline.
+ https://www.rsc.org/Merck-Index/reaction/r403/
+ https://www.wikidata.org/wiki/Q903836
+ Skraup quinoline synthesis
+ RXNO
+ RXNO:0000062
+ Skraup reaction
+
+
+
+
+ A condensation between an aromatic amine and glycerol to give a quinoline.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A homologation reaction of a carboxylic acid to give the homologated carboxylic acid via acyl chloride and diazoketone intermediates.
+ https://www.rsc.org/Merck-Index/reaction/r10/
+ https://www.wikidata.org/wiki/Q137617
+ Arndt-Eistert synthesis
+ RXNO
+ RXNO:0000063
+ This is an insertion because the carbon atom is added between the R group and the carboxyl carbon in the starting material.
+ Arndt-Eistert reaction
+
+
+
+
+ A homologation reaction of a carboxylic acid to give the homologated carboxylic acid via acyl chloride and diazoketone intermediates.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of an aldehyde or ketone with a phenylhydrazine to give an indole.
+ https://www.wikidata.org/wiki/Q901218
+ Fischer indolisation
+ Fischer indolization
+ RXNO
+ RXNO:0000064
+ Fischer indole synthesis
+
+
+
+
+ Reaction of an aldehyde or ketone with a phenylhydrazine to give an indole.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+ An intramolecular cyclisation of a diester to give a cyclic beta-ketoester.
+ https://www.rsc.org/Merck-Index/reaction/r108/
+ https://www.wikidata.org/wiki/Q900932
+ Dieckmann condensation
+ Dieckmann cyclization
+ Dieckmann reaction
+ RXNO
+ RXNO:0000065
+ This is the intramolecular version of the Claisen condensation.
+ Dieckmann cyclisation
+
+
+
+
+ An intramolecular cyclisation of a diester to give a cyclic beta-ketoester.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A joining of an organic azide and a tertiary phosphine to give a phosphazo compound.
+ https://www.wikidata.org/wiki/Q903726
+ Staudinger ligation
+ Staudinger reduction
+ RXNO
+ RXNO:0000066
+ Hydrolysis of the phosphazo compound gives the corresponding amine." [https://orcid.org/0000-0002-4077-4719, RSC:db]
+ Staudinger reaction
+
+
+
+
+ A joining of an organic azide and a tertiary phosphine to give a phosphazo compound.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A rearrangement of a hydrazobenzene to give a diaminobiphenyl compound.
+ https://www.rsc.org/Merck-Index/reaction/r33/
+ https://www.wikidata.org/wiki/Q465781
+ RXNO
+ RXNO:0000067
+ benzidine rearrangement
+
+
+
+
+ A rearrangement of a hydrazobenzene to give a diaminobiphenyl compound.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A rearrangement of a p-substituted hydrazobenzene to give a p-aminodiphenylamine.
+ https://www.rsc.org/Merck-Index/reaction/r33/
+ RXNO
+ RXNO:0000068
+ semidine rearrangement
+
+
+
+
+ A rearrangement of a p-substituted hydrazobenzene to give a p-aminodiphenylamine.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A rearrangement of a heterocyclic compound in which endocyclic and exocyclic heteroatoms swap places.
+ https://www.rsc.org/Merck-Index/reaction/r111/
+ https://www.wikidata.org/wiki/Q902659
+ RXNO
+ RXNO:0000069
+ Dimroth rearrangement
+
+
+
+
+ A rearrangement of a heterocyclic compound in which endocyclic and exocyclic heteroatoms swap places.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A molecular skeleton joining reaction in which a chain part of a molecular skeleton is lengthened.
+ RXNO
+ RXNO:0000070
+ chain lengthening
+
+
+
+
+ A molecular skeleton joining reaction in which a chain part of a molecular skeleton is lengthened.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A cleaving reaction in which a peptide is treated with phenylisothiocyanate, removing the terminal amino acid group, to form the chain-shortened amine and a phenylthiohydantoin.
+ https://www.rsc.org/Merck-Index/reaction/r122/
+ https://www.wikidata.org/wiki/Q898506
+ RXNO
+ RXNO:0000071
+ The latter can be used to identify the terminal amino acid, and the process repeated to enable peptide sequencing."
+ Edman degradation
+
+
+
+
+ A cleaving reaction in which a peptide is treated with phenylisothiocyanate, removing the terminal amino acid group, to form the chain-shortened amine and a phenylthiohydantoin.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A formylation reaction between a phenol and chloroform (for example, to form an ortho-formyl phenol).
+ https://www.rsc.org/Merck-Index/reaction/r362/
+ RXNO
+ RXNO:0000072
+ Reimer-Tiemann reaction
+
+
+
+
+ A formylation reaction between a phenol and chloroform (for example, to form an ortho-formyl phenol).
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction where atoms are lost from the molecular skeleton.
+ RXNO
+ RXNO:0000073
+ cleaving reaction
+
+
+
+
+ A reaction where atoms are lost from the molecular skeleton.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A carbon-carbon homocoupling reaction of two molecules of an alkyl halide with sodium to give a symmetrical product.
+ https://www.rsc.org/Merck-Index/reaction/r478/
+ https://www.wikidata.org/wiki/Q898901
+ Wurtz coupling
+ RXNO
+ RXNO:0000074
+ Wurtz reaction
+
+
+
+
+ A carbon-carbon homocoupling reaction of two molecules of an alkyl halide with sodium to give a symmetrical product.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A rearrangement of a 1,2-diketone to an alpha-hydroxy carboxylic acid. It can also be applied to alpha-keto aldehydes. The first exmaple of this reaction was with benzil (PhC(=O)C(=O)Ph) to form benzilic acid, hence the name.
+ https://www.rsc.org/Merck-Index/reaction/r34/
+ https://www.wikidata.org/wiki/Q818488
+ RXNO
+ RXNO:0000075
+ benzilic acid rearrangement
+
+
+
+
+ A rearrangement of a 1,2-diketone to an alpha-hydroxy carboxylic acid. It can also be applied to alpha-keto aldehydes. The first exmaple of this reaction was with benzil (PhC(=O)C(=O)Ph) to form benzilic acid, hence the name.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling of an aldehyde to an activated alkene in the presence of a nucleophilic base to give an alpha-hydroxyalkylated compound.
+ https://www.rsc.org/Merck-Index/reaction/r27/
+ https://www.wikidata.org/wiki/Q812563
+ MBH reaction
+ Morita-Baylis-Hillman reaction
+ RXNO
+ RXNO:0000076
+ Baylis-Hillman reaction
+
+
+
+
+ A carbon-carbon coupling of an aldehyde to an activated alkene in the presence of a nucleophilic base to give an alpha-hydroxyalkylated compound.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+ A coupling of an aldehyde or ketone with an alpha-halo ester to form an alpha,beta-epoxy ester, which hydrolyses to yield aldehydes or ketones by elimination of carbon dioxide.
+ https://www.rsc.org/Merck-Index/reaction/r101/
+ https://www.wikidata.org/wiki/Q899351
+ Darzens condensation
+ Darzens-Claisen reaction
+ glycidic ester condensation
+ RXNO
+ RXNO:0000077
+ Darzens reaction
+
+
+
+
+ A coupling of an aldehyde or ketone with an alpha-halo ester to form an alpha,beta-epoxy ester, which hydrolyses to yield aldehydes or ketones by elimination of carbon dioxide.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which a functional group is modified by converting it into a protecting group, in order to make subsequent reactions more selective.
+ NAMERXN:5
+ RXNO
+ RXNO:0000078
+ protection reaction
+
+
+
+
+ A reaction in which a functional group is modified by converting it into a protecting group, in order to make subsequent reactions more selective.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A protection reaction in which an amine is converted into a tert-butoxycarbonyl compound.
+ RXNO
+ RXNO:0000079
+ Boc protection
+
+
+
+
+ A protection reaction in which an amine is converted into a tert-butoxycarbonyl compound.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction in which an alpha-silyl carbanion reacts with an aldehyde or a ketone to give an alkene, proceeding via a beta-hydroxysilane. The stereochemistry of the alkene can be controlled by treating the intermediate with acid or base.
+ https://www.rsc.org/Merck-Index/reaction/r331/
+ https://www.wikidata.org/wiki/Q900350
+ Peterson reaction
+ RXNO
+ RXNO:0000080
+ Peterson olefination
+
+
+
+
+ A carbon-carbon coupling reaction in which an alpha-silyl carbanion reacts with an aldehyde or a ketone to give an alkene, proceeding via a beta-hydroxysilane. The stereochemistry of the alkene can be controlled by treating the intermediate with acid or base.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A coupling reaction in which a phenol is coupled to an aryl halide to give a diaryl ether in the presence of a copper compound.
+ https://www.wikidata.org/wiki/Q2371705
+ Ullmann ether synthesis
+ RXNO
+ RXNO:0000081
+ Ullmann condensation
+
+
+
+
+ A coupling reaction in which a phenol is coupled to an aryl halide to give a diaryl ether in the presence of a copper compound.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A coupling reaction in which an acetanilide is coupled to an aryl halide to give an N-acetyl diaryl amine in the presence of a copper compound.
+ RXNO
+ RXNO:0000082
+ Goldberg reaction
+
+
+
+
+ A coupling reaction in which an acetanilide is coupled to an aryl halide to give an N-acetyl diaryl amine in the presence of a copper compound.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A photochemical cycloaddition between an aldehyde or ketone and an alkene to give an oxetane.
+ https://www.rsc.org/Merck-Index/reaction/r319/
+ https://www.wikidata.org/wiki/Q902254
+ Paterno-Buchi reaction
+ RXNO
+ RXNO:0000083
+ Paternò–Büchi reaction
+
+
+
+
+ A photochemical cycloaddition between an aldehyde or ketone and an alkene to give an oxetane.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A joining reaction between an aldehyde or ketone and an alkyl halide or aryl halide or vinyl halide or allyl halide in the presence of metal to give a secondary or tertiary alcohol.
+ https://www.wikidata.org/wiki/Q807848
+ RXNO
+ RXNO:0000084
+ Barbier reaction
+
+
+
+
+ A joining reaction between an aldehyde or ketone and an alkyl halide or aryl halide or vinyl halide or allyl halide in the presence of metal to give a secondary or tertiary alcohol.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reductive coupling reaction between two esters to give an acyloin (an alpha-hydroxyketone).
+ https://www.rsc.org/Merck-Index/reaction/r2/
+ https://www.wikidata.org/wiki/Q345007
+ RXNO
+ RXNO:0000085
+ acyloin condensation
+
+
+
+
+ A reductive coupling reaction between two esters to give an acyloin (an alpha-hydroxyketone).
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction between a nitroalkane and an aldehyde or ketone to give a beta-hydroxy nitroalkane.
+ https://www.rsc.org/Merck-Index/reaction/r196/
+ https://www.wikidata.org/wiki/Q903747
+ nitro-aldol reaction
+ nitroaldol reaction
+ RXNO
+ RXNO:0000086
+ Henry reaction
+
+
+
+
+ A carbon-carbon coupling reaction between a nitroalkane and an aldehyde or ketone to give a beta-hydroxy nitroalkane.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The photolytic oxidation of a nitrate ester to give a gamma-nitroalcohol.
+ https://www.rsc.org/Merck-Index/reaction/r24/
+ https://www.wikidata.org/wiki/Q809549
+ RXNO
+ RXNO:0000087
+ Barton reaction
+
+
+
+
+ The photolytic oxidation of a nitrate ester to give a gamma-nitroalcohol.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction between an organohalide or organotriflate and an organozinc compound. The reaction is catalysed by palladium or nickel.
+ https://www.rsc.org/Merck-Index/reaction/r299/
+ https://www.wikidata.org/wiki/Q902756
+ Negishi cross-coupling
+ RXNO
+ RXNO:0000088
+ Negishi coupling
+
+
+
+
+ A carbon-carbon coupling reaction between an organohalide or organotriflate and an organozinc compound. The reaction is catalysed by palladium or nickel.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reduction of an aldehyde or ketone to an alcohol involving an equilibrium between the aldehyde or ketone and a reagent alcohol present in excess, catalysed by a metal alkoxide. This reaction is the reverse of the Oppenauer oxidation (RXNO:0000047).
+ https://www.rsc.org/Merck-Index/reaction/r272/
+ https://www.wikidata.org/wiki/Q903026
+ RXNO
+ RXNO:0000089
+ Meerwein-Ponndorf-Verley reduction
+
+
+
+
+ A reduction of an aldehyde or ketone to an alcohol involving an equilibrium between the aldehyde or ketone and a reagent alcohol present in excess, catalysed by a metal alkoxide. This reaction is the reverse of the Oppenauer oxidation (RXNO:0000047).
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The reaction between an alkyl halide or alkyl sulfate and a metal alkoxide to give an ether.
+ https://www.wikidata.org/wiki/Q898790
+ Williamson etherification
+ RXNO
+ RXNO:0000090
+ Williamson ether synthesis
+
+
+
+
+ The reaction between an alkyl halide or alkyl sulfate and a metal alkoxide to give an ether.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction where a carbonyl compound reacts with a phosphonium ylide to give a terminal alkene.
+ RXNO
+ RXNO:0000091
+ Wittig methylenation
+
+
+
+
+ A carbon-carbon coupling reaction where a carbonyl compound reacts with a phosphonium ylide to give a terminal alkene.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Diels-Alder reaction between a diene and an imine or an azadiene and an alkene to give a six-membered nitrogen-containing ring compound.
+ https://www.wikidata.org/wiki/Q2042393
+ aza Diels-Alder cycloaddition
+ aza Diels-Alder reaction
+ aza-Diels-Alder cycloaddition
+ azo Diels-Alder cycloaddition
+ azo Diels-Alder reaction
+ azo-Diels-Alder cycloaddition
+ azo-Diels-Alder reaction
+ RXNO
+ RXNO:0000092
+ aza-Diels-Alder reaction
+
+
+
+
+ A Diels-Alder reaction between a diene and an imine or an azadiene and an alkene to give a six-membered nitrogen-containing ring compound.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A cleaving reaction in which a skeletal atom or group of atoms is removed from the middle of a molecule.
+ https://www.wikidata.org/wiki/Q31287730
+ RXNO
+ RXNO:0000093
+ extrusion reaction
+
+
+
+
+ A cleaving reaction in which a skeletal atom or group of atoms is removed from the middle of a molecule.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ The reaction of an alpha-halosulfone to give an alkene, with the extrusion of sulfur dioxide.
+ https://www.wikidata.org/wiki/Q1935557
+ Ramberg-Backlund reaction
+ RXNO
+ RXNO:0000094
+ Ramberg-Bäcklund reaction
+
+
+
+
+ The reaction of an alpha-halosulfone to give an alkene, with the extrusion of sulfur dioxide.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The rearrangement of an aromatic nitrosamine to a para-nitrosoaniline.
+ https://www.wikidata.org/wiki/Q1968891
+ RXNO
+ RXNO:0000095
+ Fischer-Hepp rearrangement
+
+
+
+
+ The rearrangement of an aromatic nitrosamine to a para-nitrosoaniline.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A coupling reaction of a diazonium salt with a phenol or aniline to give an azo compound.
+ https://www.wikidata.org/wiki/Q668665
+ RXNO
+ RXNO:0000096
+ azo coupling
+
+
+
+
+ A coupling reaction of a diazonium salt with a phenol or aniline to give an azo compound.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction where an imine reacts with a alpha-halo ester and zinc to form a beta-amino ester.
+ imino Reformatsky reaction
+ RXNO
+ RXNO:0000097
+ imino-Reformatsky reaction
+
+
+
+
+ A carbon-carbon coupling reaction where an imine reacts with a alpha-halo ester and zinc to form a beta-amino ester.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A coupling reaction between two molecules of a terminal alkyne catalysed by Cu(I) salts.
+ https://www.rsc.org/Merck-Index/reaction/r169/
+ https://www.wikidata.org/wiki/Q514335
+ RXNO
+ RXNO:0000098
+ Glaser coupling
+
+
+
+
+ A coupling reaction between two molecules of a terminal alkyne catalysed by Cu(I) salts.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A coupling reaction between two molecules of a terminal alkyne using stoichiometric Cu(II) salts.
+ https://www.rsc.org/Merck-Index/reaction/r169/
+ Eglinton coupling
+ RXNO
+ RXNO:0000099
+ Eglinton reaction
+
+
+
+
+ A coupling reaction between two molecules of a terminal alkyne using stoichiometric Cu(II) salts.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A coupling reaction between a terminal alkyne and an alkynyl halide catalysed by Cu(I) salts.
+ https://www.rsc.org/Merck-Index/reaction/r169/
+ https://www.wikidata.org/wiki/Q903015
+ RXNO
+ RXNO:0000100
+ Cadiot-Chodkiewicz coupling
+
+
+
+
+ A coupling reaction between a terminal alkyne and an alkynyl halide catalysed by Cu(I) salts.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reductive amination of ketones or aldehydes with an ammonium formate or formamide to form an amine.
+ https://www.wikidata.org/wiki/Q726513
+ RXNO
+ RXNO:0000101
+ Leuckart reaction
+
+
+
+
+ The reductive amination of ketones or aldehydes with an ammonium formate or formamide to form an amine.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The reductive amination of ketones or aldehydes with an amine and formic acid to form amines.
+ https://www.wikidata.org/wiki/Q726513
+ Wallach reaction
+ RXNO
+ RXNO:0000102
+ Leuckart-Wallach reaction
+
+
+
+
+ The reductive amination of ketones or aldehydes with an amine and formic acid to form amines.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reaction of primary alkyl halides with sodium or potassium phthalimide, followed by hydrolysis, to give the corresponding primary amine.
+ https://www.wikidata.org/wiki/Q123422
+ RXNO
+ RXNO:0000103
+ Gabriel synthesis
+
+
+
+
+ The reaction of primary alkyl halides with sodium or potassium phthalimide, followed by hydrolysis, to give the corresponding primary amine.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The reaction of primary alkyl halides with sodium or potassium phthalimide, followed by treatment with hydrazine, to give the corresponding primary amine.
+ RXNO
+ RXNO:0000104
+ Ing-Manske procedure
+
+
+
+
+ The reaction of primary alkyl halides with sodium or potassium phthalimide, followed by treatment with hydrazine, to give the corresponding primary amine.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which a single skeletal atom is removed from the end of a chain.
+ RXNO
+ RXNO:0000105
+ end-of-chain chain shortening
+
+
+
+
+ A reaction in which a single skeletal atom is removed from the end of a chain.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ The decarboxylation of silver carboxylates with halogens to give organic halides.
+ https://www.rsc.org/Merck-Index/reaction/r215/
+ https://www.wikidata.org/wiki/Q902216
+ Borodin reaction
+ Borodine reaction
+ RXNO
+ RXNO:0000106
+ Hunsdiecker reaction
+
+
+
+
+ The decarboxylation of silver carboxylates with halogens to give organic halides.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction between a dialkyl malonate and an alkyl halide, to give a substituted acetic acid. The base/R'X treatment can be repeated to give a disubstituted product.
+ https://www.rsc.org/Merck-Index/reaction/r264/
+ https://www.wikidata.org/wiki/Q902284
+ RXNO
+ RXNO:0000107
+ malonic ester synthesis
+
+
+
+
+ A carbon-carbon coupling reaction between a dialkyl malonate and an alkyl halide, to give a substituted acetic acid. The base/R'X treatment can be repeated to give a disubstituted product.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which an existing ring is increased in size.
+ ring enlargement
+ RXNO
+ RXNO:0000108
+ ring expansion
+
+
+
+
+ A reaction in which an existing ring is increased in size.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ The reaction between isatin and an alpha-methylene carbonyl compound to give a substituted quinoline-4-carboxylic acid.
+ https://www.rsc.org/Merck-Index/reaction/r334/
+ https://www.wikidata.org/wiki/Q1580484
+ Pfitzinger quinoline synthesis
+ Pfitzinger-Borsche reaction
+ RXNO
+ RXNO:0000109
+ Pfitzinger reaction
+
+
+
+
+ The reaction between isatin and an alpha-methylene carbonyl compound to give a substituted quinoline-4-carboxylic acid.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which the parent molecule breaks up into three or more products.
+ RXNO
+ RXNO:0000110
+ fragmentation reaction
+
+
+
+
+ A reaction in which the parent molecule breaks up into three or more products.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ The fragmentation of a molecule that takes place when an electron-donating fragment (X) and an electron-accepting fragment (X') are situated at positions 1 and 3 on an aliphatic chain, to give a cationic fragment, a neutral fragment (e.g. an alkene) and an anionic fragment.
+ https://www.wikidata.org/wiki/Q5609896
+ RXNO
+ RXNO:0000111
+ Grob fragmentation
+
+
+
+
+ The fragmentation of a molecule that takes place when an electron-donating fragment (X) and an electron-accepting fragment (X') are situated at positions 1 and 3 on an aliphatic chain, to give a cationic fragment, a neutral fragment (e.g. an alkene) and an anionic fragment.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+ The rearrangement of an alpha-, beta- or gamma-hydroxy silane to give a silyl ether. It is catalysed by a base.
+ https://www.rsc.org/Merck-Index/reaction/r62/
+ https://www.wikidata.org/wiki/Q2558021
+ RXNO
+ RXNO:0000113
+ Brook rearrangement
+
+
+
+
+ The rearrangement of an alpha-, beta- or gamma-hydroxy silane to give a silyl ether. It is catalysed by a base.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reaction of a propargylic cation (stabilised with dicobalt octacarbonyl) with a nucleophile to give a substituted alkyne.
+ https://www.rsc.org/Merck-Index/reaction/r303/
+ https://www.wikidata.org/wiki/Q902932
+ RXNO
+ RXNO:0000114
+ Nicholas reaction
+
+
+
+
+ The reaction of a propargylic cation (stabilised with dicobalt octacarbonyl) with a nucleophile to give a substituted alkyne.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The reaction of a propargylic cation (stabilised with dicobalt octacarbonyl) with a hydride or amine or enamine to give a substituted alkyne.
+ RXNO
+ RXNO:0000115
+ Nicholas reaction, nucleophilic heteroatom centre
+
+
+
+
+ The reaction of a propargylic cation (stabilised with dicobalt octacarbonyl) with a hydride or amine or enamine to give a substituted alkyne.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+ The reaction of a propargylic cation (stabilised with dicobalt octacarbonyl) with a nucleophilic carbon centre (on e.g. enolates, allyl silanes, ketones, electron-rich aromatics, beta-dicarbonyl compounds) to give a substituted alkyne.
+ RXNO
+ RXNO:0000116
+ Nicholas reaction, nucleophilic carbon centre
+
+
+
+
+ The reaction of a propargylic cation (stabilised with dicobalt octacarbonyl) with a nucleophilic carbon centre (on e.g. enolates, allyl silanes, ketones, electron-rich aromatics, beta-dicarbonyl compounds) to give a substituted alkyne.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction between a phenyl sulfone and an aldehyde or ketone to give a (typically trans) alkene.
+ https://www.rsc.org/Merck-Index/reaction/r224/
+ https://www.wikidata.org/wiki/Q902237
+ Julia-Lythgoe olefination
+ RXNO
+ RXNO:0000117
+ Julia olefination
+
+
+
+
+ A carbon-carbon coupling reaction between a phenyl sulfone and an aldehyde or ketone to give a (typically trans) alkene.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The oxidation of a benzylic halide to give an aldehyde. The reaction uses hexamethylenetetramine.
+ https://www.wikidata.org/wiki/Q909040
+ RXNO
+ RXNO:0000118
+ Sommelet reaction
+
+
+
+
+ The oxidation of a benzylic halide to give an aldehyde. The reaction uses hexamethylenetetramine.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reduction of an ester using sodium to give two alcohols.
+ https://www.rsc.org/Merck-Index/reaction/r58/
+ https://www.wikidata.org/wiki/Q895315
+ Bouveault-Blanc procedure
+ Bouveault-Blanc reduction
+ RXNO
+ RXNO:0000119
+ Bouveault-Blanc reaction
+
+
+
+
+ The reduction of an ester using sodium to give two alcohols.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A base-catalysed isomerisation of a 2,3-epoxyalcohol, with inversion of configuration at C2.
+ https://www.rsc.org/Merck-Index/reaction/r321/
+ https://www.wikidata.org/wiki/Q983127
+ RXNO
+ RXNO:0000120
+ Payne rearrangement
+
+
+
+
+ A base-catalysed isomerisation of a 2,3-epoxyalcohol, with inversion of configuration at C2.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A base-catalysed isomerisation of a 2,3-epoxyamine to form a hydroxy aziridine, with inversion of configuration at C2.
+ https://www.rsc.org/Merck-Index/reaction/r321/
+ RXNO
+ RXNO:0000121
+ aza-Payne rearrangement
+
+
+
+
+ A base-catalysed isomerisation of a 2,3-epoxyamine to form a hydroxy aziridine, with inversion of configuration at C2.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The base-catalysed rearrangement of an o-acetoxyacetophenone to give a hydroxyphenyl-1,3-diketone.
+ https://www.rsc.org/Merck-Index/reaction/r14/
+ https://www.wikidata.org/wiki/Q804325
+ RXNO
+ RXNO:0000122
+ Baker-Venkataraman rearrangement
+
+
+
+
+ The base-catalysed rearrangement of an o-acetoxyacetophenone to give a hydroxyphenyl-1,3-diketone.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which two or more groups of atoms are removed from the molecule, resulting in a change of skeletal bond order.
+ RXNO
+ RXNO:0000123
+ This is narrower in focus than elimination in general in that we're focussing on the aims of the chemist.
+ molecular skeleton elimination reaction
+
+
+
+
+ A reaction in which two or more groups of atoms are removed from the molecule, resulting in a change of skeletal bond order.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reaction of a tosylhydrazone of an aldehyde or ketone with a strong base to give an olefin.
+ https://www.rsc.org/Merck-Index/reaction/r16/
+ https://www.wikidata.org/wiki/Q575939
+ RXNO
+ RXNO:0000124
+ This generally provides the more-substituted olefin as the thermodynamic product.
+ Bamford-Stevens reaction
+
+
+
+
+ The reaction of a tosylhydrazone of an aldehyde or ketone with a strong base to give an olefin.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reaction of a tosylhydrazone of an aldehyde or ketone with an alkyllithium or Grignard reagent to give an olefin.
+ https://www.rsc.org/Merck-Index/reaction/r16/
+ https://www.wikidata.org/wiki/Q846597
+ RXNO
+ RXNO:0000125
+ This generally provides the less-substituted olefin as the kinetic product.
+ Shapiro reaction
+
+
+
+
+ The reaction of a tosylhydrazone of an aldehyde or ketone with an alkyllithium or Grignard reagent to give an olefin.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reaction between an aromatic amine, an aldehyde and pyruvic acid on heating to give a quinoline 4-carboxylic acid (cinchoninic acid).
+ https://www.rsc.org/Merck-Index/reaction/r114/
+ https://www.wikidata.org/wiki/Q3772250
+ RXNO
+ RXNO:0000126
+ Doebner reaction
+
+
+
+
+ The reaction between an aromatic amine, an aldehyde and pyruvic acid on heating to give a quinoline 4-carboxylic acid (cinchoninic acid).
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The conversion of an aromatic amine to the corresponding fluoride via the diazonium fluoroborate.
+ https://www.rsc.org/Merck-Index/reaction/r388/
+ https://www.wikidata.org/wiki/Q572113
+ Schiemann reaction
+ RXNO
+ RXNO:0000127
+ Balz-Schiemann reaction
+
+
+
+
+ The conversion of an aromatic amine to the corresponding fluoride via the diazonium fluoroborate.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The decarboxylation and coupling of a carboxylate or mixture of carboxylates to give a dimer.
+ https://www.rsc.org/Merck-Index/reaction/r238/
+ https://www.wikidata.org/wiki/Q901771
+ Crum-Brown-Walker reaction
+ Kolbe electrolytic synthesis
+ Kolbe electrosynthesis
+ Kolbe reaction
+ RXNO
+ RXNO:0000128
+ Kolbe electrolysis
+
+
+
+
+ The decarboxylation and coupling of a carboxylate or mixture of carboxylates to give a dimer.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of a ketone or aldehyde, amine, an isocyanide and carboxylic acid to form a bisamide.
+ https://www.rsc.org/Merck-Index/reaction/r440/
+ https://www.wikidata.org/wiki/Q2002373
+ 4CC
+ Ugi four-component condensation
+ Ugi-4CR
+ RXNO
+ RXNO:0000129
+ Ugi reaction
+
+
+
+
+ Reaction of a ketone or aldehyde, amine, an isocyanide and carboxylic acid to form a bisamide.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The oxidation of a terminal alkene or ethene to a methyl ketone or acetaldehyde, catalysed by PdCl2 and CuCl2, and using molecular oxygen as the oxidant.
+ https://www.rsc.org/Merck-Index/reaction/r452/
+ Wacker oxidation
+ Wacker reaction
+ RXNO
+ RXNO:0000130
+ Wacker-Tsuji oxidation
+
+
+
+
+ The oxidation of a terminal alkene or ethene to a methyl ketone or acetaldehyde, catalysed by PdCl2 and CuCl2, and using molecular oxygen as the oxidant.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The oxidation of ethene to acetaldehyde, catalysed by PdCl2 and CuCl2, and using molecular oxygen as the oxidant.
+ https://www.wikidata.org/wiki/Q578923
+ RXNO
+ RXNO:0000131
+ Wacker process
+
+
+
+
+ The oxidation of ethene to acetaldehyde, catalysed by PdCl2 and CuCl2, and using molecular oxygen as the oxidant.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reaction of formaldehyde with methanol to form acetic acid, catalysed by a rhodium complex.
+ https://www.wikidata.org/wiki/Q901246
+ RXNO
+ RXNO:0000132
+ Monsanto process
+
+
+
+
+ The reaction of formaldehyde with methanol to form acetic acid, catalysed by a rhodium complex.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reaction of formaldehyde with methanol to form acetic acid, catalysed by an iridium complex.
+ https://www.wikidata.org/wiki/Q579304
+ RXNO
+ RXNO:0000133
+ Cativa process
+
+
+
+
+ The reaction of formaldehyde with methanol to form acetic acid, catalysed by an iridium complex.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The deoxygenation of an alcohol to the corresponding alkane using a thiochloroformate. It proceeds by a radical mechanism.
+ https://www.rsc.org/Merck-Index/reaction/r22/
+ https://www.wikidata.org/wiki/Q809548
+ Barton deoxygenation
+ Barton reduction
+ RXNO
+ RXNO:0000134
+ Barton-McCombie deoxygenation
+
+
+
+
+ The deoxygenation of an alcohol to the corresponding alkane using a thiochloroformate. It proceeds by a radical mechanism.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The decarboxylation of a carboxylic acid to the lower homologue alkane using a pyridine thione.
+ https://www.rsc.org/Merck-Index/reaction/r21/
+ https://www.wikidata.org/wiki/Q3454335
+ RXNO
+ RXNO:0000135
+ The reaction proceeds by a radical mechanism.
+ Barton decarboxylation
+
+
+
+
+ The decarboxylation of a carboxylic acid to the lower homologue alkane using a pyridine thione.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The hydrogenolysis of an acyl halide to the corresponding aldehyde, catalysed by palladium-on-barium sulfate.
+ https://www.rsc.org/Merck-Index/reaction/r375/
+ https://www.wikidata.org/wiki/Q905524
+ Rosenmund reaction
+ RXNO
+ RXNO:0000136
+ Rosenmund reduction
+
+
+
+
+ The hydrogenolysis of an acyl halide to the corresponding aldehyde, catalysed by palladium-on-barium sulfate.
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction where a terminal alkyne reacts with an aryl halide to give an aryl alkyne. It is catalysed by palladium.
+ NAMERXN:3.3
+ https://www.rsc.org/Merck-Index/reaction/r408/
+ https://www.wikidata.org/wiki/Q900334
+ Hagihara-Sonogashira coupling
+ Sonogashira cross-coupling
+ Sonogashira reaction
+ RXNO
+ RXNO:0000137
+ Sonogashira coupling
+
+
+
+
+ A carbon-carbon coupling reaction where a terminal alkyne reacts with an aryl halide to give an aryl alkyne. It is catalysed by palladium.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction between two aromatic aldehydes to give a benzoin (an alpha-hydroxyketone).
+ https://www.rsc.org/Merck-Index/reaction/r35/
+ https://www.wikidata.org/wiki/Q818514
+ benzoin addition
+ RXNO
+ RXNO:0000138
+ benzoin condensation
+
+
+
+
+ A reaction between two aromatic aldehydes to give a benzoin (an alpha-hydroxyketone).
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The formylation of an arene with hydrogen cyanide to give an aryl aldehyde or ketone.
+ RXNO
+ RXNO:0000139
+ This is essentially a variant of the Friedel-Crafts acylation.
+ Gattermann reaction
+
+
+
+
+ The formylation of an arene with hydrogen cyanide to give an aryl aldehyde or ketone.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The coupling of a boronic acid or boronic ester with an unsaturated halide, triflate or sulfonate catalysed by a palladium(0) complex.
+ NAMERXN:3.1
+ https://www.rsc.org/Merck-Index/reaction/r424/
+ https://www.wikidata.org/wiki/Q899891
+ Suzuki coupling reaction
+ Suzuki cross-coupling
+ Suzuki cross-coupling reaction
+ Suzuki reaction
+ Suzuki-Miyaura coupling
+ Suzuki-Miyaura coupling reaction
+ Suzuki-Miyaura cross-coupling
+ Suzuki-Miyaura cross-coupling reaction
+ Suzuki-Miyaura reaction
+ RXNO
+ RXNO:0000140
+ Suzuki-Miyaura coupling
+
+
+
+
+ The coupling of a boronic acid or boronic ester with an unsaturated halide, triflate or sulfonate catalysed by a palladium(0) complex.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The epoxidation of an allylic alcohol to give a beta,gamma-epoxy alcohol, with control of absolute stereochemistry at the two new stereocentres. The oxidising agent is tert-butyl hydroperoxide, and the catalyst is a complex of titanium salt and optically active diethyl tartrate.
+ https://www.rsc.org/Merck-Index/reaction/r397/
+ https://www.wikidata.org/wiki/Q56672072
+ Katsuki-Sharpless asymmetric epoxidation
+ Katsuki-Sharpless epoxidation
+ Sharpless epoxidation
+ Sharpless-Katsuki asymmetric epoxidation
+ Sharpless-Katsuki epoxidation
+ RXNO
+ RXNO:0000141
+ Sharpless asymmetric epoxidation
+
+
+
+
+ The epoxidation of an allylic alcohol to give a beta,gamma-epoxy alcohol, with control of absolute stereochemistry at the two new stereocentres. The oxidising agent is tert-butyl hydroperoxide, and the catalyst is a complex of titanium salt and optically active diethyl tartrate.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The dihydroxylation of an alkene to give an alpha,beta-diol, with control of absolute stereochemistry at the two new stereocentres. The oxidising agent is osmium tetroxide, which is used catalytically with a stoichiometric oxidant and a chiral ligand. The reagents are available commercially as AD-mix.
+ https://www.rsc.org/Merck-Index/reaction/r396/
+ https://www.wikidata.org/wiki/Q752651
+ Sharpless bishydroxylation
+ Sharpless hydroxylation
+ RXNO
+ RXNO:0000142
+ Sharpless asymmetric dihydroxylation
+
+
+
+
+ The dihydroxylation of an alkene to give an alpha,beta-diol, with control of absolute stereochemistry at the two new stereocentres. The oxidising agent is osmium tetroxide, which is used catalytically with a stoichiometric oxidant and a chiral ligand. The reagents are available commercially as AD-mix.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The aminohydroxylation of an alkene to give a beta-amino alcohol, with control of absolute stereochemistry at the two new stereocentres. The oxidising agent is an oxygen-containing osmium species and/or an amino derivative which can be used catalytically with a stoichiometric oxidant and a chiral ligand.
+ Sharpless oxyamination
+ RXNO
+ RXNO:0000143
+ Sharpless asymmetric aminohydroxylation
+
+
+
+
+ The aminohydroxylation of an alkene to give a beta-amino alcohol, with control of absolute stereochemistry at the two new stereocentres. The oxidising agent is an oxygen-containing osmium species and/or an amino derivative which can be used catalytically with a stoichiometric oxidant and a chiral ligand.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A cross-coupling reaction between a Grignard reagent and an activated (aryl or vinyl) halide or triflate. The reaction is catalysed by a palladium or nickel catalyst.
+ https://www.rsc.org/Merck-Index/reaction/r248/
+ https://www.wikidata.org/wiki/Q899278
+ Kharasch cross-coupling
+ Kumada cross-coupling
+ RXNO
+ RXNO:0000144
+ Kumada coupling
+
+
+
+
+ A cross-coupling reaction between a Grignard reagent and an activated (aryl or vinyl) halide or triflate. The reaction is catalysed by a palladium or nickel catalyst.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The degradation of a carboxylic acid to its next lower homologous carboxylic acid.
+ https://www.rsc.org/Merck-Index/reaction/r18/
+ https://www.wikidata.org/wiki/Q5801440
+ Barbier-Wieland procedure
+ RXNO
+ RXNO:0000145
+ Barbier-Wieland degradation
+
+
+
+
+ The degradation of a carboxylic acid to its next lower homologous carboxylic acid.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A homologation reaction of an aldehyde to yield a terminal alkyne. The reagents are tetrabromomethane, triphenylphosphine, butyllithium and water.
+ https://www.rsc.org/Merck-Index/reaction/r89/
+ https://www.wikidata.org/wiki/Q903573
+ Ramirez-Corey-Fuchs reaction
+ RXNO
+ RXNO:0000146
+ Corey-Fuchs reaction
+
+
+
+
+ A homologation reaction of an aldehyde to yield a terminal alkyne. The reagents are tetrabromomethane, triphenylphosphine, butyllithium and water.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A reduction of a quaternary ammonium salt containing at least one unsaturated substituent, to give a tertiary amine.
+ https://www.rsc.org/Merck-Index/reaction/r127/
+ https://www.wikidata.org/wiki/Q2026108
+ Emde reaction
+ Emde reduction
+ RXNO
+ RXNO:0000147
+ Emde degradation
+
+
+
+
+ A reduction of a quaternary ammonium salt containing at least one unsaturated substituent, to give a tertiary amine.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+ The [3,3]-sigmatropic rearrangement of an allyl vinyl ether to give a gamma,delta-unsaturated carbonyl compound.
+ https://www.rsc.org/Merck-Index/reaction/r80/
+ https://www.wikidata.org/wiki/Q900936
+ RXNO
+ RXNO:0000148
+ Claisen rearrangement
+
+
+
+
+ The [3,3]-sigmatropic rearrangement of an allyl vinyl ether to give a gamma,delta-unsaturated carbonyl compound.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+ The enolisation and subsequent [3,3]-sigmatropic rearrangement of an allylic acetate to give a gamma,delta-unsaturated carboxylic acid.
+ https://www.rsc.org/Merck-Index/reaction/r80/
+ https://www.wikidata.org/wiki/Q1945726
+ RXNO
+ RXNO:0000149
+ Ireland-Claisen rearrangement
+
+
+
+
+ The enolisation and subsequent [3,3]-sigmatropic rearrangement of an allylic acetate to give a gamma,delta-unsaturated carboxylic acid.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which one or more atoms are added to the molecular skeleton and a skeletal rearrangement occurs.
+ RXNO
+ RXNO:0000150
+ joining with rearrangement
+
+
+
+
+ A reaction in which one or more atoms are added to the molecular skeleton and a skeletal rearrangement occurs.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ The coupling and subsequent [3,3]-sigmatropic rearrangement of an allylic ether or allylic thioether or allylic amine and a ketene to give the corresponding gamma,delta-unsaturated carbonyl compound.
+ RXNO
+ RXNO:0000151
+ Bellus-Claisen rearrangement
+
+
+
+
+ The coupling and subsequent [3,3]-sigmatropic rearrangement of an allylic ether or allylic thioether or allylic amine and a ketene to give the corresponding gamma,delta-unsaturated carbonyl compound.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+ The coupling and subsequent [3,3]-sigmatropic rearrangement of an allylic alcohol and alpha,alpha-dialkoxy ethylamine to give a gamma,delta-unsaturated dialkyl amide.
+ https://www.rsc.org/Merck-Index/reaction/r80/
+ RXNO
+ RXNO:0000152
+ Eschenmoser-Claisen rearrangement
+
+
+
+
+ The coupling and subsequent [3,3]-sigmatropic rearrangement of an allylic alcohol and alpha,alpha-dialkoxy ethylamine to give a gamma,delta-unsaturated dialkyl amide.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+ The coupling and subsequent [3,3]-sigmatropic rearrangement of an allylic alcohol and trimethyl orthoacetate to give a gamma,delta-unsaturated alkyl ester.
+ https://www.rsc.org/Merck-Index/reaction/r80/
+ RXNO
+ RXNO:0000153
+ Johnson-Claisen rearrangement
+
+
+
+
+ The coupling and subsequent [3,3]-sigmatropic rearrangement of an allylic alcohol and trimethyl orthoacetate to give a gamma,delta-unsaturated alkyl ester.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+ The oxidation of a primary alcohol or secondary alcohol to an aldehyde or ketone respectively. Does not work with allylic or benzylic alcohols.
+ https://www.rsc.org/Merck-Index/reaction/r426
+ RXNO
+ RXNO:0000154
+ Swern oxidation
+
+
+
+
+ The oxidation of a primary alcohol or secondary alcohol to an aldehyde or ketone respectively. Does not work with allylic or benzylic alcohols.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The conversion of an alkyl chloride, alkyl bromide or alkyl sulfonate ester to an alkyl iodide by SN2 substitution. The reaction relies upon the equilibrium being pushed to completion by the precipitation.
+ https://www.rsc.org/Merck-Index/reaction/r141/
+ RXNO
+ RXNO:0000155
+ Finkelstein reaction
+
+
+
+
+ The conversion of an alkyl chloride, alkyl bromide or alkyl sulfonate ester to an alkyl iodide by SN2 substitution. The reaction relies upon the equilibrium being pushed to completion by the precipitation.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The derivatisation (for example with tosyl chloride) and subsequent rearrangement of a hydroxamic acid to give an isocyanate.
+ https://www.rsc.org/Merck-Index/reaction/r259/
+ RXNO
+ RXNO:0000156
+ Lossen rearrangement
+
+
+
+
+ The derivatisation (for example with tosyl chloride) and subsequent rearrangement of a hydroxamic acid to give an isocyanate.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The conversion of a primary nitroalkane or secondary nitroalkane to an aldehyde or ketone, respectively.
+ https://www.rsc.org/Merck-Index/reaction/r297/
+ RXNO
+ RXNO:0000157
+ Nef reaction
+
+
+
+
+ The conversion of a primary nitroalkane or secondary nitroalkane to an aldehyde or ketone, respectively.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The reaction of a doubly activated methylene compound that has at least one carbonyl substituent with an aryl azide to give a hydrazone. Usually there is concomitant cleaving and oxidation of one of the carbonyl substituents.
+ RXNO
+ RXNO:0000158
+ Japp-Klingemann reaction
+
+
+
+
+ The reaction of a doubly activated methylene compound that has at least one carbonyl substituent with an aryl azide to give a hydrazone. Usually there is concomitant cleaving and oxidation of one of the carbonyl substituents.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The formation of a quinoline from a primary aromatic amine and an alpha,beta-unsaturated carbonyl compound.
+ Doebner-von Miller reaction
+ Skraup-Doebner-von Miller quinoline synthesis
+ RXNO
+ RXNO:0000159
+ Doebner-Miller reaction
+
+
+
+
+ The formation of a quinoline from a primary aromatic amine and an alpha,beta-unsaturated carbonyl compound.
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The protection of an amine (often a peptide) as its 9H-fluoren-9-ylmethoxycarbonyl derivative.
+ RXNO
+ RXNO:0000160
+ Fmoc protection
+
+
+
+
+ The protection of an amine (often a peptide) as its 9H-fluoren-9-ylmethoxycarbonyl derivative.
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The cyclisation of a 1,4-dicarbonyl compound with another molecule to give a five-membered aromatic ring compound.
+ RXNO
+ RXNO:0000161
+ Usually this gives rise to a heterocycle.
+ Paal-Knorr synthesis
+
+
+
+
+ The cyclisation of a 1,4-dicarbonyl compound with another molecule to give a five-membered aromatic ring compound.
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The cyclisation of a 1,4-dicarbonyl compound with an acid catalyst to give a furan.
+ https://www.rsc.org/Merck-Index/reaction/r315/
+ RXNO
+ RXNO:0000162
+ Paal-Knorr furan synthesis
+
+
+
+
+ The cyclisation of a 1,4-dicarbonyl compound with an acid catalyst to give a furan.
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The cyclisation of a 1,4-dicarbonyl compound with phosphorus pentasulfide to give a thiophene.
+ RXNO
+ RXNO:0000163
+ Paal-Knorr thiophene synthesis
+
+
+
+
+ The cyclisation of a 1,4-dicarbonyl compound with phosphorus pentasulfide to give a thiophene.
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The cyclisation of a 1,4-dicarbonyl compound with an amine to give a pyrrole.
+ https://www.rsc.org/Merck-Index/reaction/r316/
+ RXNO
+ RXNO:0000164
+ Merck Index says "ammonia or primary amines"
+ Paal-Knorr pyrrole synthesis
+
+
+
+
+ The cyclisation of a 1,4-dicarbonyl compound with an amine to give a pyrrole.
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The coupling of an alcohol or amine with an acyl chloride to give an ester or amide. A two-phase solvent system is often used, to enable the acid generated during the reaction to be neutralised by the aqueous base, while the starting materials and products remain in the organic phase.
+ https://www.rsc.org/Merck-Index/reaction/r392/
+ RXNO
+ RXNO:0000165
+ Schotten-Baumann reaction
+
+
+
+
+ The coupling of an alcohol or amine with an acyl chloride to give an ester or amide. A two-phase solvent system is often used, to enable the acid generated during the reaction to be neutralised by the aqueous base, while the starting materials and products remain in the organic phase.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The elimination of a methylated amine from an alkylamine to form an olefin. The reaction proceeds via the quaternary ammonium salt.
+ https://www.rsc.org/Merck-Index/reaction/r205/
+ exhaustive methylation
+ RXNO
+ Hofmann degradation
+ RXNO:0000166
+ Hofmann elimination
+
+
+
+
+ The elimination of a methylated amine from an alkylamine to form an olefin. The reaction proceeds via the quaternary ammonium salt.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The esterification of a carboxylic acid with an alcohol. Various Lewis acids or Bronsted acids may be used as catalyst.
+ Fischer esterification
+ RXNO
+ RXNO:0000167
+ Fischer-Speier esterification
+
+
+
+
+ The esterification of a carboxylic acid with an alcohol. Various Lewis acids or Bronsted acids may be used as catalyst.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The degradation of an alpha-hydroxy amide or an alpha,beta-unsaturated amide to the lower homologue aldehyde, especially in carbohydrate chemistry. The process proceeds via Hofmann degradation.
+ Weerman degradation
+ Weerman's reaction
+ RXNO
+ RXNO:0000168
+ Weerman reaction
+
+
+
+
+ The degradation of an alpha-hydroxy amide or an alpha,beta-unsaturated amide to the lower homologue aldehyde, especially in carbohydrate chemistry. The process proceeds via Hofmann degradation.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reaction of ortho- or para-phenolic (or ortho- or para-anilinic) aldehydes or ketones with hydrogen peroxide to form bisphenols (or hydroxy anilines) and carboxylic acids.
+ RXNO
+ RXNO:0000169
+ Dakin reaction
+
+
+
+
+ The reaction of ortho- or para-phenolic (or ortho- or para-anilinic) aldehydes or ketones with hydrogen peroxide to form bisphenols (or hydroxy anilines) and carboxylic acids.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The reaction of a carboxylic acid with hydrazoic acid to give the lower homologue amine, with the loss of the terminal carbon atom.
+ RXNO
+ RXNO:0000170
+ Schmidt rearrangement, carboxylic acid
+
+
+
+
+ The reaction of a carboxylic acid with hydrazoic acid to give the lower homologue amine, with the loss of the terminal carbon atom.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The reaction of a ketone with hydrazoic acid with the insertion of an NH group between the carbonyl carbon and one of the R groups to form an amide.
+ RXNO
+ RXNO:0000171
+ Schmidt rearrangement, ketone
+
+
+
+
+ The reaction of a ketone with hydrazoic acid with the insertion of an NH group between the carbonyl carbon and one of the R groups to form an amide.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The reaction of a tertiary alcohol with hydrazoic acid with rearrangement to form an imide.
+ RXNO
+ RXNO:0000172
+ Schmidt rearrangement, tertiary alcohol
+
+
+
+
+ The reaction of a tertiary alcohol with hydrazoic acid with rearrangement to form an imide.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The reaction of an alkene with hydrazoic acid with rearrangement to form an imide.
+ RXNO
+ RXNO:0000173
+ Schmidt rearrangement, alkene
+
+
+
+
+ The reaction of an alkene with hydrazoic acid with rearrangement to form an imide.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The [2,3]-sigmatropic rearrangement of a benzyl quaternary ammonium salt to form an aniline.
+ RXNO
+ RXNO:0000174
+ Sommelet-Hauser rearrangement
+
+
+
+
+ The [2,3]-sigmatropic rearrangement of a benzyl quaternary ammonium salt to form an aniline.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reaction of an amino acid with an acid anhydride to give an alpha-acylamido ketone. The reaction proceeds via the mixed anhydride and an oxazolone; the product is always racemic.
+ RXNO
+ RXNO:0000175
+ Dakin-West reaction
+
+
+
+
+ The reaction of an amino acid with an acid anhydride to give an alpha-acylamido ketone. The reaction proceeds via the mixed anhydride and an oxazolone; the product is always racemic.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The cleavage of an oxime to the corresponding nitrile and an alkyl halide. This reaction is related to the Beckmann rearrangement, and occurs when the R group that is anti to the oxime hydroxyl is quaternary.
+ RXNO
+ RXNO:0000176
+ Beckmann fragmentation
+
+
+
+
+ The cleavage of an oxime to the corresponding nitrile and an alkyl halide. This reaction is related to the Beckmann rearrangement, and occurs when the R group that is anti to the oxime hydroxyl is quaternary.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The transfer of a hydrogen or halogen atom from a haloalkane to an alkene, giving the chain-extended halogenated alkane.
+ Kharasch addition reaction
+ RXNO
+ RXNO:0000177
+ Kharasch reaction
+
+
+
+
+ The transfer of a hydrogen or halogen atom from a haloalkane to an alkene, giving the chain-extended halogenated alkane.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The allylic oxidation of an alkene with a peroxy ester or a peroxide to give the corresponding allylic alcohol derivative. The catalyst is a copper compound.
+ RXNO
+ RXNO:0000178
+ Kharasch-Sosnovsky reaction
+
+
+
+
+ The allylic oxidation of an alkene with a peroxy ester or a peroxide to give the corresponding allylic alcohol derivative. The catalyst is a copper compound.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The oxidation of a phenol to give a (predominantly para) diphenol using potassium persulfate.
+ RXNO
+ RXNO:0000179
+ Elbs persulfate oxidation, phenol variant
+
+
+
+
+ The oxidation of a phenol to give a (predominantly para) diphenol using potassium persulfate.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The oxidation of a methyl-substituted aromatic compound to the corresponding benzaldehyde using potassium persulfate.
+ RXNO
+ RXNO:0000180
+ Elbs persulfate oxidation, tolyl variant
+
+
+
+
+ The oxidation of a methyl-substituted aromatic compound to the corresponding benzaldehyde using potassium persulfate.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The oxidation of an aromatic amine to give a (predominantly ortho) amino aryl sulfate using potassium persulfate followed by hydrolysis to yield the corresponding aminophenol.
+ https://www.rsc.org/Merck-Index/reaction/r59/
+ RXNO
+ RXNO:0000181
+ Boyland-Sims oxidation
+
+
+
+
+ The oxidation of an aromatic amine to give a (predominantly ortho) amino aryl sulfate using potassium persulfate followed by hydrolysis to yield the corresponding aminophenol.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The (predominantly ortho) carboxylation of a phenoxide.
+ https://www.rsc.org/Merck-Index/reaction/r239/
+ RXNO
+ RXNO:0000182
+ Kolbe-Schmitt reaction
+
+
+
+
+ The (predominantly ortho) carboxylation of a phenoxide.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The reaction between an alpha-halocarbonyl compound and a trialkyl phosphite to give an enol phosphate.
+ https://www.rsc.org/Merck-Index/reaction/r329/
+ RXNO
+ RXNO:0000183
+ not clear why this is where it is and not a sibling of the Arbuzov reaction (2014-02-17)
+ Perkow reaction
+
+
+
+
+ The reaction between an alpha-halocarbonyl compound and a trialkyl phosphite to give an enol phosphate.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The oxidation of a primary or secondary alcohol to the corresponding aldehyde or ketone respectively using dimethyl sulfoxide, 1,3-dicyclohexylcarbodiimide and acid. The reaction proceeds via an alkoxysulfonium ylide.
+ https://www.rsc.org/Merck-Index/reaction/r335/
+ Moffatt oxidation
+ RXNO
+ RXNO:0000184
+ Pfitzner-Moffatt oxidation
+
+
+
+
+ The oxidation of a primary or secondary alcohol to the corresponding aldehyde or ketone respectively using dimethyl sulfoxide, 1,3-dicyclohexylcarbodiimide and acid. The reaction proceeds via an alkoxysulfonium ylide.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The conversion of an aryl alkyl ketone to an amide and/or an ammonium salt of a carboxylic acid using ammonium polysulfide. The carbonyl group of the product is always at the end of the alkyl chain.
+ RXNO
+ RXNO:0000185
+ Willgerodt reaction
+
+
+
+
+ The conversion of an aryl alkyl ketone to an amide and/or an ammonium salt of a carboxylic acid using ammonium polysulfide. The carbonyl group of the product is always at the end of the alkyl chain.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The conversion of an aryl alkyl ketone to an amide using sulfur and dry ammonia or a primary or secondary amine. The amide carbonyl group is always at the end of the alkyl chain.
+ https://www.rsc.org/Merck-Index/reaction/r466/
+ RXNO
+ RXNO:0000186
+ Willgerodt-Kindler reaction
+
+
+
+
+ The conversion of an aryl alkyl ketone to an amide using sulfur and dry ammonia or a primary or secondary amine. The amide carbonyl group is always at the end of the alkyl chain.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The formation of an ester from two aldehydes via a disproportionation process using a metal alkoxide to oxidise one aldehyde and reduce the other.
+ https://www.rsc.org/Merck-Index/reaction/r433/
+ RXNO
+ RXNO:0000187
+ Tishchenko reaction
+
+
+
+
+ The formation of an ester from two aldehydes via a disproportionation process using a metal alkoxide to oxidise one aldehyde and reduce the other.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The reaction between a methylene ketone and a polynitro aromatic compound.
+ https://www.rsc.org/Merck-Index/reaction/r482/
+ RXNO
+ RXNO:0000188
+ Zimmermann reaction
+
+
+
+
+ The reaction between a methylene ketone and a polynitro aromatic compound.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The rearrangement of the sulfonic ester of a ketoxime in base to give an alpha-amino ketone.
+ https://www.rsc.org/Merck-Index/reaction/r296/
+ RXNO
+ RXNO:0000189
+ Neber rearrangement
+
+
+
+
+ The rearrangement of the sulfonic ester of a ketoxime in base to give an alpha-amino ketone.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A coupling reaction of an aldehyde to an allyl, vinyl or aryl halide or triflate in the presence of chromium(II). It is catalysed by nickel.
+ Nozaki reaction
+ Nozaki-Hiyama-Kishi coupling
+ Nozaki-Kishi reaction
+ RXNO
+ RXNO:0000191
+ Nozaki-Hiyama-Kishi reaction
+
+
+
+
+ A coupling reaction of an aldehyde to an allyl, vinyl or aryl halide or triflate in the presence of chromium(II). It is catalysed by nickel.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which an aryl halide or aryl triflate reacts with a primary or secondary amine in the presence of base to give a secondary or tertiary amine. It is catalysed by a palladium catalyst.
+ Buchwald-Hartwig reaction
+ RXNO
+ RXNO:0000192
+ Buchwald-Hartwig amination
+
+
+
+
+ A reaction in which an aryl halide or aryl triflate reacts with a primary or secondary amine in the presence of base to give a secondary or tertiary amine. It is catalysed by a palladium catalyst.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction where an organosilane reacts with an organic halide or triflate. It is catalysed by a palladium or nickel complex.
+ Hiyama cross-coupling
+ RXNO
+ RXNO:0000193
+ Hiyama coupling
+
+
+
+
+ A carbon-carbon coupling reaction where an organosilane reacts with an organic halide or triflate. It is catalysed by a palladium or nickel complex.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The 1,2-rearrangement of an alpha-methylene ammonium salt or alpha-methylene sulfonium salt to an amine or sulfide in the presence of strong base.
+ RXNO
+ RXNO:0000194
+ Stevens rearrangement
+
+
+
+
+ The 1,2-rearrangement of an alpha-methylene ammonium salt or alpha-methylene sulfonium salt to an amine or sulfide in the presence of strong base.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The 1,2-rearrangement of an alpha-methylene ammonium salt to an amine in the presence of strong base.
+ RXNO
+ RXNO:0000195
+ Stevens rearrangement, ammonium
+
+
+
+
+ The 1,2-rearrangement of an alpha-methylene ammonium salt to an amine in the presence of strong base.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The 1,2-rearrangement of an alpha-methylene sulfonium salt to a sulfide in the presence of strong base.
+ RXNO
+ RXNO:0000196
+ Stevens rearrangement, sulfonium
+
+
+
+
+ The 1,2-rearrangement of an alpha-methylene sulfonium salt to a sulfide in the presence of strong base.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+ A [3,3]-sigmatropic rearrangement where an aza-1,5-hexadiene rearranges to form an aza-1,5-hexadiene.
+ RXNO
+ RXNO:0000197
+ aza-Cope rearrangement
+
+
+
+
+ A [3,3]-sigmatropic rearrangement where an aza-1,5-hexadiene rearranges to form an aza-1,5-hexadiene.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The rearrangement of a 2-aza-1,5-hexadiene to form an imine.
+ RXNO
+ RXNO:0000198
+ 2-aza-Cope rearrangement
+
+
+
+
+ The rearrangement of a 2-aza-1,5-hexadiene to form an imine.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The rearrangement of a 3-aza-1,5-hexadiene to form a delta,epsilon-unsaturated imine.
+ amino-Claisen rearrangement
+ aza-Claisen rearrangement
+ RXNO
+ RXNO:0000199
+ This is the reverse of the 1-aza-Cope rearrangement.
+ 3-aza-Cope rearrangement
+
+
+
+
+ The rearrangement of a 3-aza-1,5-hexadiene to form a delta,epsilon-unsaturated imine.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The rearrangement of a delta,epsilon-unsaturated imine to form a 3-aza-1,5-hexadiene.
+ RXNO
+ RXNO:0000200
+ This is the reverse of the 3-aza-Cope rearrangement.
+ 1-aza-Cope rearrangement
+
+
+
+
+ The rearrangement of a delta,epsilon-unsaturated imine to form a 3-aza-1,5-hexadiene.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The rearrangement of an oxazolyl carbonate to a C-carboxyazlactone.
+ RXNO
+ RXNO:0000201
+ Steglich rearrangement
+
+
+
+
+ The rearrangement of an oxazolyl carbonate to a C-carboxyazlactone.
+ RSC:jrw
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which the number of rings in a molecule stays the same but the connectivity of the atoms in at least one ring changes.
+ RXNO
+ RXNO:0000202
+ ring rearrangement
+
+
+
+
+ A reaction in which the number of rings in a molecule stays the same but the connectivity of the atoms in at least one ring changes.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which a protecting group is modified by converting it into a functional group.
+ NAMERXN:6
+ RXNO
+ RXNO:0000203
+ deprotection reaction
+
+
+
+
+ A reaction in which a protecting group is modified by converting it into a functional group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A joining reaction in which two carbon-carbon multiple bonds are redistributed among two fragments. The reaction is typically catalysed by a metal carbenoid, and proceeds via two four-membered intermediates (metallacyclobutanes). The reaction is driven by release of a low-MW alkene.
+ metathesis
+ multiple bond metathesis
+ RXNO
+ RXNO:0000204
+ multiple-bond metathesis
+
+
+
+
+ A joining reaction in which two carbon-carbon multiple bonds are redistributed among two fragments. The reaction is typically catalysed by a metal carbenoid, and proceeds via two four-membered intermediates (metallacyclobutanes). The reaction is driven by release of a low-MW alkene.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A planned reaction step in which the product has fewer rings than the reactants.
+ ring opening
+ selective ring opening
+ RXNO
+ RXNO:0000205
+ ring breaking
+
+
+
+
+ A planned reaction step in which the product has fewer rings than the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A planned reaction step in which an existing ring is reduced in size.
+ RXNO
+ RXNO:0000206
+ ring contraction
+
+
+
+
+ A planned reaction step in which an existing ring is reduced in size.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An addition reaction between a carbonyl compound, an inorganic cyanide and an ammonium salt, followed by hydrolysis, to give an alpha-amino carboxylic acid.
+ RXNO
+ RXNO:0000207
+ Strecker reaction
+
+
+
+
+ An addition reaction between a carbonyl compound, an inorganic cyanide and an ammonium salt, followed by hydrolysis, to give an alpha-amino carboxylic acid.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+ The [3,3]-sigmatropic rearrangement, and subsequent re-aromatisation, of an allyl aryl ether to give an ortho-allyl phenol.
+ RXNO
+ RXNO:0000208
+ aromatic Claisen rearrangement
+
+
+
+
+ The [3,3]-sigmatropic rearrangement, and subsequent re-aromatisation, of an allyl aryl ether to give an ortho-allyl phenol.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The acid-catalysed cyclisation of a divinylketone to give a cyclopentenone.
+ https://www.rsc.org/Merck-Index/reaction/r295/
+ Nazarov cyclization
+ RXNO
+ RXNO:0000209
+ Nazarov cyclisation
+
+
+
+
+ The acid-catalysed cyclisation of a divinylketone to give a cyclopentenone.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The stereospecific oxidation of a (phenyldimethylsilyl)alkane to the corresponding alcohol using bromine, usually generated in situ from potassium bromide and peracetic acid.
+ https://www.rsc.org/Merck-Index/reaction/r150/
+ Fleming oxidation
+ Tamao-Fleming oxidation
+ RXNO
+ RXNO:0000210
+ Fleming-Tamao oxidation
+
+
+
+
+ The stereospecific oxidation of a (phenyldimethylsilyl)alkane to the corresponding alcohol using bromine, usually generated in situ from potassium bromide and peracetic acid.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The stereospecific oxidation of a (halosilyl)alkane to the corresponding alcohol using potassium fluoride and hydrogen peroxide.
+ https://www.rsc.org/Merck-Index/reaction/r150/
+ Tamao-Kumada oxidation
+ RXNO
+ RXNO:0000211
+ Tamao oxidation
+
+
+
+
+ The stereospecific oxidation of a (halosilyl)alkane to the corresponding alcohol using potassium fluoride and hydrogen peroxide.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction in which an aldehyde or ketone reacts with allyltrimethylsilane to form a homoallylic alcohol.
+ RXNO
+ RXNO:0000212
+ Sakurai reaction, aldehyde or ketone
+
+
+
+
+ A carbon-carbon coupling reaction in which an aldehyde or ketone reacts with allyltrimethylsilane to form a homoallylic alcohol.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction in which an enone reacts with allyltrimethylsilane to form a delta,epsilon-unsaturated carbonyl compound.
+ RXNO
+ RXNO:0000213
+ Sakurai reaction, enone
+
+
+
+
+ A carbon-carbon coupling reaction in which an enone reacts with allyltrimethylsilane to form a delta,epsilon-unsaturated carbonyl compound.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction in which an acid chloride reacts with allyltrimethylsilane to form a gamma,delta-unsaturated ketone.
+ RXNO
+ RXNO:0000214
+ Sakurai reaction, acid chloride
+
+
+
+
+ A carbon-carbon coupling reaction in which an acid chloride reacts with allyltrimethylsilane to form a gamma,delta-unsaturated ketone.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction in which an acetal or ketal reacts with allyltrimethylsilane to form a homoallylic ether.
+ RXNO
+ RXNO:0000215
+ Sakurai reaction, acetal or ketal
+
+
+
+
+ A carbon-carbon coupling reaction in which an acetal or ketal reacts with allyltrimethylsilane to form a homoallylic ether.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction in which an imine reacts with allyltrimethylsilane to form a homoallylic amine.
+ RXNO
+ RXNO:0000216
+ imine Sakurai reaction
+
+
+
+
+ A carbon-carbon coupling reaction in which an imine reacts with allyltrimethylsilane to form a homoallylic amine.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+ A ring-breaking reaction in which an epoxide reacts with allyltrimethylsilane to form a hydroxy alkene.
+ RXNO
+ RXNO:0000217
+ Sakurai reaction, epoxide
+
+
+
+
+ A ring-breaking reaction in which an epoxide reacts with allyltrimethylsilane to form a hydroxy alkene.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The disproportionation of a non-enolisable aldehyde to the corresponding carboxylic acid and alcohol. The reaction is base-catalysed.
+ https://www.rsc.org/Merck-Index/reaction/r71/
+ RXNO
+ RXNO:0000218
+ Cannizzaro reaction
+
+
+
+
+ The disproportionation of a non-enolisable aldehyde to the corresponding carboxylic acid and alcohol. The reaction is base-catalysed.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reaction between two different non-enolisable aldehydes to give a carboxylic acid and an alcohol. The reaction is base-catalysed.
+ https://www.rsc.org/Merck-Index/reaction/r71/
+ RXNO
+ RXNO:0000219
+ crossed Cannizzaro reaction
+
+
+
+
+ The reaction between two different non-enolisable aldehydes to give a carboxylic acid and an alcohol. The reaction is base-catalysed.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The conversion of a sulfoxide with an alpha-hydrogen to an alpha-substituted thioether. The reaction is usually performed with an acid anhydride or acyl halide.
+ Pummerer methyl sulfoxide rearrangement
+ RXNO
+ RXNO:0000220
+ Pummerer rearrangement
+
+
+
+
+ The conversion of a sulfoxide with an alpha-hydrogen to an alpha-substituted thioether. The reaction is usually performed with an acid anhydride or acyl halide.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reaction of a tertiary amine oxide with an anhydride or acyl chloride to give an N,N-disubstituted acetamide and an aldehyde.
+ RXNO
+ RXNO:0000221
+ Polonovski reaction
+
+
+
+
+ The reaction of a tertiary amine oxide with an anhydride or acyl chloride to give an N,N-disubstituted acetamide and an aldehyde.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reaction of a tertiary amine oxide with trifluoroacetic anhydride to give an N,N-disubstituted acetamide and an aldehyde.
+ Potier-Polonovski reaction
+ RXNO
+ RXNO:0000222
+ Polonovski-Potier reaction
+
+
+
+
+ The reaction of a tertiary amine oxide with trifluoroacetic anhydride to give an N,N-disubstituted acetamide and an aldehyde.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The alkylation of a tertiary amine with an alkyl halide to the corresponding ammonium salt.
+ RXNO:0000375
+ https://www.rsc.org/Merck-Index/reaction/r275/
+ Menschutkin reaction
+ RXNO
+ RXNO:0000223
+ Menshutkin reaction
+
+
+
+
+ The alkylation of a tertiary amine with an alkyl halide to the corresponding ammonium salt.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The deamination and decarboxylation of amino acids to imines and then to aldehydes or ketones, in the presence of a carbonyl compound (especially an alpha,beta-dicarbonyl compound or a reducing sugar such as glucose). The reaction is involved in the generation of meat aromas/flavours in cooking.
+ RXNO
+ RXNO:0000224
+ Strecker degradation
+
+
+
+
+ The deamination and decarboxylation of amino acids to imines and then to aldehydes or ketones, in the presence of a carbonyl compound (especially an alpha,beta-dicarbonyl compound or a reducing sugar such as glucose). The reaction is involved in the generation of meat aromas/flavours in cooking.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The allylic or benzylic bromination of hydrocarbons using an N-bromoimide and a radical initiator, to give an allylic or benzylic bromide.
+ Wohl-Ziegler reaction
+ RXNO
+ RXNO:0000225
+ Wohl-Ziegler bromination
+
+
+
+
+ The allylic or benzylic bromination of hydrocarbons using an N-bromoimide and a radical initiator, to give an allylic or benzylic bromide.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The reduction of an aldehyde or ketone to the corresponding methylene compound, using hydrazine hydrate and a base.
+ RXNO
+ RXNO:0000226
+ Wolff-Kishner reduction
+
+
+
+
+ The reduction of an aldehyde or ketone to the corresponding methylene compound, using hydrazine hydrate and a base.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The reduction of an aldehyde or ketone to the corresponding methylene compound, using hydrazine hydrate and a base in refluxing ethylene glycol.
+ Huang-Minlon modification
+ RXNO
+ RXNO:0000227
+ Wolff-Kishner reduction, Huang-Minlon modification
+
+
+
+
+ The reduction of an aldehyde or ketone to the corresponding methylene compound, using hydrazine hydrate and a base in refluxing ethylene glycol.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The reduction of an ester to the corresponding alcohol, using sodium methoxide in dry methanol.
+ Zemplen procedure
+ RXNO
+ RXNO:0000228
+ Zemplen transesterification
+
+
+
+
+ The reduction of an ester to the corresponding alcohol, using sodium methoxide in dry methanol.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The rearrangement of an O-alkenyl acetal to give the corresponding beta-alkoxy carbonyl compound.
+ Ferrier reaction
+ RXNO
+ RXNO:0000229
+ Ferrier rearrangement
+
+
+
+
+ The rearrangement of an O-alkenyl acetal to give the corresponding beta-alkoxy carbonyl compound.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The rearrangement of an O-alkenyl hemiaminal ether to give the corresponding beta-amino carbonyl compound.
+ aza-Ferrier reaction
+ RXNO
+ RXNO:0000230
+ aza-Ferrier rearrangement
+
+
+
+
+ The rearrangement of an O-alkenyl hemiaminal ether to give the corresponding beta-amino carbonyl compound.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A joining reaction where an N=C system with an allylic hydrogen reacts with a compound containing a multiple bond (an enophile) to form a substituted alkene.
+ RXNO
+ RXNO:0000231
+ aza-ene reaction
+
+
+
+
+ A joining reaction where an N=C system with an allylic hydrogen reacts with a compound containing a multiple bond (an enophile) to form a substituted alkene.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The alkylation of an amine with a boronic acid and an aldehyde to give a substituted amine.
+ Petasis three-component coupling
+ RXNO
+ RXNO:0000232
+ Petasis reaction
+
+
+
+
+ The alkylation of an amine with a boronic acid and an aldehyde to give a substituted amine.
+ RSC:db
+
+
+
+
+
+
+
+
+ A rearrangement of a furfuryl alcohol derivative to a dihydropyranone, from which monosaccharides may be synthesised.
+ RXNO
+ RXNO:0000233
+ Achmatowicz rearrangement
+
+
+
+
+ A rearrangement of a furfuryl alcohol derivative to a dihydropyranone, from which monosaccharides may be synthesised.
+ RSC:db
+
+
+
+
+
+
+
+
+ A rearrangement of a furfuryl amine derivative to a tetrahydropyridinone.
+ RXNO
+ RXNO:0000234
+ aza-Achmatowicz rearrangement
+
+
+
+
+ A rearrangement of a furfuryl amine derivative to a tetrahydropyridinone.
+ RSC:db
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction between a nitroalkane and an imine to give a beta-amino nitroalkane.
+ RXNO
+ RXNO:0000235
+ aza-Henry reaction
+
+
+
+
+ A carbon-carbon coupling reaction between a nitroalkane and an imine to give a beta-amino nitroalkane.
+ RSC:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A three-component coupling of a beta-keto ester, an aldehyde and urea to give a 3,4-dihydropyrimidinone.
+ https://www.rsc.org/Merck-Index/reaction/r43/
+ Biginelli condensation
+ Biginelli pyrimidone synthesis
+ Biginelli three-component reaction
+ RXNO
+ RXNO:0000236
+ Biginelli reaction
+
+
+
+
+ A three-component coupling of a beta-keto ester, an aldehyde and urea to give a 3,4-dihydropyrimidinone.
+ RSC:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The coupling of an alpha-bromo ester with a nitrile to give a beta-ketoester, in the presence of zinc.
+ RXNO
+ RXNO:0000237
+ Blaise reaction
+
+
+
+
+ The coupling of an alpha-bromo ester with a nitrile to give a beta-ketoester, in the presence of zinc.
+ RSC:db
+
+
+
+
+
+
+
+
+ The substitution of an amine with a nucleophile using a pyrylium salt.
+ RXNO
+ RXNO:0000238
+ Katritzky pyrylium-pyridinium method
+
+
+
+
+ The substitution of an amine with a nucleophile using a pyrylium salt.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The rearrangement of a 3-aza-4-metalla-1,5-hexadiene to form a delta,epsilon-unsaturated metallaimine.
+ RXNO
+ RXNO:0000239
+ metalla-aza-Claisen rearrangement
+
+
+
+
+ The rearrangement of a 3-aza-4-metalla-1,5-hexadiene to form a delta,epsilon-unsaturated metallaimine.
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The cyclisation of an ene-diyne to give a 1,4-diradical cyclohexatriene. The diradical usually aromatises.
+ https://www.rsc.org/Merck-Index/reaction/r37/
+ Bergman cyclization
+ Bergman reaction
+ Masamune-Bergman cyclisation
+ Masamune-Bergman cyclization
+ RXNO
+ RXNO:0000240
+ Bergman cyclisation
+
+
+
+
+ The cyclisation of an ene-diyne to give a 1,4-diradical cyclohexatriene. The diradical usually aromatises.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A conjugate addition reaction where a carbon nucleophile adds to an alpha,beta-unsaturated nitro compound.
+ RXNO
+ RXNO:0000241
+ nitro-Michael reaction
+
+
+
+
+ A conjugate addition reaction where a carbon nucleophile adds to an alpha,beta-unsaturated nitro compound.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The homogeneous asymmetric catalytic hydrogenation of a C=C double bond using a ruthenium(II) BINAP catalyst.
+ Noyori hydrogenation, alkene
+ RXNO
+ RXNO:0000242
+ Noyori asymmetric hydrogenation, alkene
+
+
+
+
+ The homogeneous asymmetric catalytic hydrogenation of a C=C double bond using a ruthenium(II) BINAP catalyst.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The homogeneous asymmetric catalytic hydrogenation of a carbonyl bond using a ruthenium(II) BINAP catalyst.
+ Noyori hydrogenation, carbonyl
+ RXNO
+ RXNO:0000243
+ Noyori asymmetric hydrogenation, carbonyl
+
+
+
+
+ The homogeneous asymmetric catalytic hydrogenation of a carbonyl bond using a ruthenium(II) BINAP catalyst.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The reaction between an isonitrile, a carboxylic acid and aldehyde or ketone to give an alpha-acyloxy amide.
+ RXNO
+ RXNO:0000244
+ Passerini reaction
+
+
+
+
+ The reaction between an isonitrile, a carboxylic acid and aldehyde or ketone to give an alpha-acyloxy amide.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A joining reaction in which two carbon-carbon double bonds in the same molecule are redistributed to give a cycloalkene. It is typically catalysed by a metal carbenoid, and proceeds via two four-membered intermediates (metallacyclobutanes). The reaction is driven by release of a low-MW alkene.
+ RCM
+ ring closing alkene metathesis
+ ring closing metathesis
+ ring closing olefin metathesis
+ ring-closing alkene metathesis
+ ring-closing olefin metathesis
+ RXNO
+ RXNO:0000245
+ ring-closing metathesis
+
+
+
+
+ A joining reaction in which two carbon-carbon double bonds in the same molecule are redistributed to give a cycloalkene. It is typically catalysed by a metal carbenoid, and proceeds via two four-membered intermediates (metallacyclobutanes). The reaction is driven by release of a low-MW alkene.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A joining reaction, the objective of which is that a large number of monomers react together to produce a polymer consisting of repeating units.
+ polymerisation
+ polymerization
+ polymerization reaction
+ RXNO
+ RXNO:0000246
+ polymerisation reaction
+
+
+
+
+ A joining reaction, the objective of which is that a large number of monomers react together to produce a polymer consisting of repeating units.
+ rsc:db
+
+
+
+
+
+
+
+
+ A joining reaction in which two carbon-carbon double bonds are redistributed among two fragments, i.e. two alkenes. It is typically catalysed by a metal carbenoid, and proceeds via two four-membered intermediates (metallacyclobutanes). The reaction is driven by release of ring strain in the cycloalkene.
+ ROMP
+ ring-opening metathesis polymerization
+ RXNO
+ RXNO:0000247
+ ring-opening metathesis polymerisation
+
+
+
+
+ A joining reaction in which two carbon-carbon double bonds are redistributed among two fragments, i.e. two alkenes. It is typically catalysed by a metal carbenoid, and proceeds via two four-membered intermediates (metallacyclobutanes). The reaction is driven by release of ring strain in the cycloalkene.
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+ An adaptation of the Claisen rearrangement that transforms a beta-keto allyl ester into a gamma,delta-allyl ketone. It uses base and high temperature or milder conditions with a ruthenium or palladium complex as catalyst.
+ https://www.rsc.org/Merck-Index/reaction/r72/
+ Kimel-Cope rearrangement
+ RXNO
+ RXNO:0000248
+ Carroll rearrangement
+
+
+
+
+ An adaptation of the Claisen rearrangement that transforms a beta-keto allyl ester into a gamma,delta-allyl ketone. It uses base and high temperature or milder conditions with a ruthenium or palladium complex as catalyst.
+ RSC:db
+
+
+
+
+
+
+
+
+ A Mitsunobu reaction, where an alcohol is converted to something else with inversion at the stereocentre, using diphenylphosphoryl azide.
+ RXNO
+ RXNO:0000249
+ Bose-Mitsunobu reaction
+
+
+
+
+ A Mitsunobu reaction, where an alcohol is converted to something else with inversion at the stereocentre, using diphenylphosphoryl azide.
+ RSC:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The rearrangement of a 2-bromoalkene into an alkyne, mediated by strong base.
+ https://www.rsc.org/Merck-Index/reaction/r161/
+ https://www.wikidata.org/wiki/Q573664
+ RXNO
+ RXNO:0000250
+ Fritsch-Buttenberg-Wiechell rearrangement
+
+
+
+
+ The rearrangement of a 2-bromoalkene into an alkyne, mediated by strong base.
+ RSC:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction where an aldehyde reacts with a phosphonium salt to give a Z-iodoalkene. The reaction is mediated by sodium or potassium hexamethyldisilazide.
+ RXNO
+ RXNO:0000251
+ Stork-Wittig olefination
+
+
+
+
+ A carbon-carbon coupling reaction where an aldehyde reacts with a phosphonium salt to give a Z-iodoalkene. The reaction is mediated by sodium or potassium hexamethyldisilazide.
+ RSC:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reduction of a 2-nitrobiaryl compound to give a carbazole.
+ RXNO
+ RXNO:0000252
+ Cadogan carbazole synthesis
+
+
+
+
+ The reduction of a 2-nitrobiaryl compound to give a carbazole.
+ doi:10.1039/JR9650004831
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The arylation of an arylamine mediated by isopentyl nitrite.
+ RXNO
+ RXNO:0000253
+ Cadogan coupling
+
+
+
+
+ The arylation of an arylamine mediated by isopentyl nitrite.
+ doi:10.1039/b409373a
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The reaction between a 1,9-diformyldipyrromethane and a dipyrromethane to give a porphodimethene.
+ RXNO
+ RXNO:0000254
+ MacDonald condensation
+
+
+
+
+ The reaction between a 1,9-diformyldipyrromethane and a dipyrromethane to give a porphodimethene.
+ doi:10.1039/a908784b
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ The carbon-carbon homocoupling reaction of a pair of alkyne molecules using a borane and iodine. The reaction proceeds via a borane intermediate.
+ RXNO
+ RXNO:0000255
+ Zweifel diene synthesis
+
+
+
+
+ The carbon-carbon homocoupling reaction of a pair of alkyne molecules using a borane and iodine. The reaction proceeds via a borane intermediate.
+ https://orcid.org/0000-0002-4077-4719
+ isbn:9780521096430
+
+
+
+
+
+
+
+
+
+ The oxidation of a primary alcohol to an aldehyde or a secondary alcohol to a ketone using the Dess-Martin periodinane.
+ https://www.rsc.org/Merck-Index/reaction/r107/
+ https://www.wikidata.org/wiki/Q28455131
+ Dess-Martin periodinane oxidation
+ RXNO
+ RXNO:0000256
+ Dess-Martin oxidation
+
+
+
+
+ The oxidation of a primary alcohol to an aldehyde or a secondary alcohol to a ketone using the Dess-Martin periodinane.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ The oxidative cleavage of an alpha,beta-diol using lead tetraacetate to give the corresponding carbonyl compounds.
+ https://www.rsc.org/Merck-Index/reaction/r96/
+ https://www.wikidata.org/wiki/Q30693026
+ Criegee glycol cleavage
+ Criegee reaction
+ RXNO
+ RXNO:0000257
+ Criegee oxidation
+
+
+
+
+ The oxidative cleavage of an alpha,beta-diol using lead tetraacetate to give the corresponding carbonyl compounds.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A ring formation reaction where an alkene reacts with a dihalomethane in the presence of a metal atom or metal complexes to form a cyclopropane. The traditional reaction uses a zinc-copper couple and diiodomethane.
+ https://www.rsc.org/Merck-Index/reaction/r400/
+ https://www.wikidata.org/wiki/Q903776
+ Simmons-Smith cyclopropanation
+ RXNO
+ RXNO:0000258
+ Simmons-Smith reaction
+
+
+
+
+ A ring formation reaction where an alkene reacts with a dihalomethane in the presence of a metal atom or metal complexes to form a cyclopropane. The traditional reaction uses a zinc-copper couple and diiodomethane.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ Any of a family of sigmatropic rearrangements that involve the migration of a group on an electronegative atom (O or N) to a carbon atom.
+ RXNO
+ RXNO:0000259
+ Wittig rearrangement
+
+
+
+
+ Any of a family of sigmatropic rearrangements that involve the migration of a group on an electronegative atom (O or N) to a carbon atom.
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A base-mediated 1,2-sigmatropic rearrangement of an ether to give an alcohol.
+ 1,2-Wittig rearrangement
+ [1,2] Wittig rearrangement
+ RXNO
+ RXNO:0000260
+ [1,2]-Wittig rearrangement
+
+
+
+
+ A base-mediated 1,2-sigmatropic rearrangement of an ether to give an alcohol.
+ rsc:db
+
+
+
+
+
+
+
+
+ A base-mediated 2,3-sigmatropic rearrangement of an allyl ether to give a homoallylic alcohol.
+ 2,3-Wittig rearrangement
+ [2,3] Wittig rearrangement
+ RXNO
+ RXNO:0000261
+ [2,3]-Wittig rearrangement
+
+
+
+
+ A base-mediated 2,3-sigmatropic rearrangement of an allyl ether to give a homoallylic alcohol.
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A base-mediated 1,2-sigmatropic rearrangement of a tertiary amine to give a secondary amine.
+ 1,2-aza-Wittig rearrangement
+ [1,2] aza-Wittig rearrangement
+ RXNO
+ RXNO:0000262
+ [1,2]-aza-Wittig rearrangement
+
+
+
+
+ A base-mediated 1,2-sigmatropic rearrangement of a tertiary amine to give a secondary amine.
+ rsc:db
+
+
+
+
+
+
+
+
+ A base-mediated 2,3-sigmatropic rearrangement of an activated tertiary allyl amine, to give a secondary homoallylic amine.
+ 2,3-aza-Wittig rearrangement
+ [2,3] aza-Wittig rearrangement
+ RXNO
+ RXNO:0000263
+ [2,3]-aza-Wittig rearrangement
+
+
+
+
+ A base-mediated 2,3-sigmatropic rearrangement of an activated tertiary allyl amine, to give a secondary homoallylic amine.
+ rsc:db
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling of an imine to an activated alkene in the presence of a nucleophilic base to give an allylic amine.
+ aza-Morita-Baylis-Hillman reaction
+ RXNO
+ RXNO:0000264
+ aza-Baylis-Hillman reaction
+
+
+
+
+ A carbon-carbon coupling of an imine to an activated alkene in the presence of a nucleophilic base to give an allylic amine.
+ rsc:db
+
+
+
+
+
+
+
+
+ Reaction of a carbonyl compound with a phosphazene to give an imine.
+ RXNO
+ RXNO:0000265
+ aza-Wittig reaction
+
+
+
+
+ Reaction of a carbonyl compound with a phosphazene to give an imine.
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An oxidation reaction involving Fenton's reagent.
+ RXNO:0000267
+ Fenton's reaction
+ RXNO
+ RXNO:0000266
+ Fenton reaction
+
+
+
+
+ An oxidation reaction involving Fenton's reagent.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A ring-forming reaction between two equivalents of a beta-ketoester, an aldehyde and ammonia (or an ammonium salt), to give a dihydropyridine. The dihydropyridine can be oxidised to a pyridine using an oxidising agent.
+ Hantzsch dihydropyridine synthesis
+ RXNO
+ RXNO:0000268
+ Hantzsch pyridine synthesis
+
+
+
+
+ A ring-forming reaction between two equivalents of a beta-ketoester, an aldehyde and ammonia (or an ammonium salt), to give a dihydropyridine. The dihydropyridine can be oxidised to a pyridine using an oxidising agent.
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A [3+2] cycloaddition reaction between an azide and an alkyne to give a 1,2,3-triazole, needing only heat to proceed.
+ Huisgen cycloaddition
+ Huisgen reaction
+ Huisgen's 1,3-dipolar cycloaddition
+ "click" reaction
+ 'click' reaction
+ alkyne-azide Huisgen cycloaddition
+ alkyne-azide Huisgen reaction
+ azide-alkyne Huisgen cycloaddition
+ azide-alkyne Huisgen reaction
+ azide-alkyne click reaction
+ click reaction
+ RXNO
+ RXNO:0000269
+ Note: The term "click reaction" was originally used in a broader sense to refer to any coupling that took place cleanly and quickly in quantitative yield, but it now always seems to be used in this narrower sense.
+ alkyne-azide click reaction
+
+
+
+
+ A [3+2] cycloaddition reaction between an azide and an alkyne to give a 1,2,3-triazole, needing only heat to proceed.
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A [3+2] cycloaddition reaction between an azide and an alkyne to give a 1,2,3-triazole as a single regioisomer.
+ CuAAC
+ copper(I)-catalysed alkyne-azide cycloaddition
+ copper(I)-catalysed azide-alkyne click reaction
+ copper(I)-catalysed azide-alkyne cycloaddition
+ copper(I)-catalyzed alkyne-azide cycloaddition
+ copper(I)-catalyzed azide-alkyne click reaction
+ copper(I)-catalyzed azide-alkyne cycloaddition
+ RXNO
+ RXNO:0000270
+ Commonly described as a variant of the (uncatalyzed) alkyne-azide click reaction, the mechanism of reaction is different, and thus formally it is not a 1,3-dipolar cycloaddition. [rsc:db]
+ copper(I)-catalyzed azide-alkyne cycloaddition
+
+
+
+
+ A [3+2] cycloaddition reaction between an azide and an alkyne to give a 1,2,3-triazole as a single regioisomer.
+ RSC:db
+
+
+
+
+
+
+
+
+ A process in which carbon monoxide and hydrogen ('syngas') are converted into various liquid hydrocarbons.
+ Fischer-Tropsch reaction
+ Fischer-Tropsch synthesis
+ RXNO
+ RXNO:0000271
+ Fischer-Tropsch process
+
+
+
+
+ A process in which carbon monoxide and hydrogen ('syngas') are converted into various liquid hydrocarbons.
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reaction of hydrogen and carbon monoxide with an alkene, to give an aldehyde, catalysed by a rhodium or cobalt catalyst. The process is equivalent to the formal addition of the H-C bond of formaldehyde across the double bond of an alkene.
+ RXNO
+ RXNO:0000272
+ hydroformylation
+
+
+
+
+ The reaction of hydrogen and carbon monoxide with an alkene, to give an aldehyde, catalysed by a rhodium or cobalt catalyst. The process is equivalent to the formal addition of the H-C bond of formaldehyde across the double bond of an alkene.
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reverse of a [4+2] cycloaddition reaction, in which an unsaturated six-membered ring compound fragments to give a diene and a compound containing a double or triple bond (a dienophile).
+ retro Diels-Alder reaction
+ RXNO
+ RXNO:0000273
+ retro-Diels-Alder reaction
+
+
+
+
+ The reverse of a [4+2] cycloaddition reaction, in which an unsaturated six-membered ring compound fragments to give a diene and a compound containing a double or triple bond (a dienophile).
+ rsc:db
+
+
+
+
+
+
+
+
+ The reverse of an aldol addition, in which a beta-hydroxy ketone fragments to form a carbonyl compound and the enolate of an alpha-acidic carbonyl compound.
+ retro-aldol reaction
+ RXNO
+ RXNO:0000274
+ This process can occur because the whole reaction is an equilibrium. In the forward direction (aldol addition), elimination of water from the beta-hydroxy ketone, giving an alpha,beta-unsaturated ketone, is irreversible, and thus the aldol condensation does not have a "retro" counterpart.
+ retro-aldol addition
+
+
+
+
+ The reverse of an aldol addition, in which a beta-hydroxy ketone fragments to form a carbonyl compound and the enolate of an alpha-acidic carbonyl compound.
+ rsc:db
+
+
+
+
+
+
+
+
+ A hydrogenation in which a metal-ligating group distant from the reacting alkene directs the attack of hydrogen, giving preferentially one stereoisomer of the product.
+ RXNO
+ RXNO:0000275
+ Stork-Crabtree hydrogenation
+
+
+
+
+ A hydrogenation in which a metal-ligating group distant from the reacting alkene directs the attack of hydrogen, giving preferentially one stereoisomer of the product.
+ doi:10.1021/jo00364a007
+ rsc:db
+
+
+
+
+
+
+
+
+ The insertion of alkenes (usually ethene) into the Al-C bond of an aluminium alkyl, to give a long-chain aluminium alkyl that can go on to react again, or can decompose into the corresponding terminal alkene. The addition of transition metals results in reliable production of high molecular weight polymers.
+ "Aufbau" reaction
+ 'Aufbau' reaction
+ Aufbau process
+ RXNO
+ RXNO:0000276
+ Aufbau reaction
+
+
+
+
+ The insertion of alkenes (usually ethene) into the Al-C bond of an aluminium alkyl, to give a long-chain aluminium alkyl that can go on to react again, or can decompose into the corresponding terminal alkene. The addition of transition metals results in reliable production of high molecular weight polymers.
+ rsc:db
+
+
+
+
+
+
+
+
+ The reaction of an aluminium alkyl with an alkene, to give an intermediate aluminium species that can give various products after work-up.
+ RXNO
+ RXNO:0000277
+ hydroalumination
+
+
+
+
+ The reaction of an aluminium alkyl with an alkene, to give an intermediate aluminium species that can give various products after work-up.
+ rsc:db
+
+
+
+
+
+
+
+
+ The reaction of two alkenes to give an elongated alkene, employing a transition-metal-based catalyst.
+ 1,2-hydrovinylation
+ RXNO
+ RXNO:0000278
+ hydrovinylation
+
+
+
+
+ The reaction of two alkenes to give an elongated alkene, employing a transition-metal-based catalyst.
+ rsc:db
+
+
+
+
+
+
+
+
+ The reaction of a 1,3-diene with an alkene to give a 1,4-diene, usually employing a cobalt-based catalyst (see Hilt and Luers, Synthesis, 2002, 609).
+ RXNO
+ RXNO:0000279
+ 1,4-hydrovinylation
+
+
+
+
+ The reaction of a 1,3-diene with an alkene to give a 1,4-diene, usually employing a cobalt-based catalyst (see Hilt and Luers, Synthesis, 2002, 609).
+ rsc:db
+
+
+
+
+
+
+
+
+ A joining reaction in which two carbon-carbon double bonds are redistributed among two fragments, i.e. two alkenes. It is typically catalysed by a metal carbenoid, and proceeds via two four-membered intermediates (metallacyclobutanes). The reaction is driven by release of a low-MW alkene.
+ Grubbs metathesis
+ Grubbs reaction
+ cross metathesis
+ cross-metathesis
+ olefin metathesis
+ transalkylidenation
+ RXNO
+ RXNO:0000280
+ alkene metathesis
+
+
+
+
+ A joining reaction in which two carbon-carbon double bonds are redistributed among two fragments, i.e. two alkenes. It is typically catalysed by a metal carbenoid, and proceeds via two four-membered intermediates (metallacyclobutanes). The reaction is driven by release of a low-MW alkene.
+ rsc:db
+
+
+
+
+
+
+
+
+ A joining reaction in which two carbon-carbon triple bonds are redistributed among two fragments, i.e. two alkynes. It is catalysed by a metal carbenoid, and proceeds via two four-membered intermediates (metallacyclobutenes). The reaction is driven by release of a low-MW alkyne.
+ RXNO
+ RXNO:0000281
+ alkyne metathesis
+
+
+
+
+ A joining reaction in which two carbon-carbon triple bonds are redistributed among two fragments, i.e. two alkynes. It is catalysed by a metal carbenoid, and proceeds via two four-membered intermediates (metallacyclobutenes). The reaction is driven by release of a low-MW alkyne.
+ rsc:db
+
+
+
+
+
+
+
+
+ A joining reaction in which a carbon-carbon double bond and a carbon-carbon triple bond are redistributed among two fragments, i.e. an alkene and an alkyne. It is typically catalysed by a metal carbenoid, and proceeds via two four-membered intermediates (metallacyclobutenes). As a low-MW alkene is not released, the reaction is usually driven by formation of a ring.
+ RXNO
+ RXNO:0000282
+ enyne metathesis
+
+
+
+
+ A joining reaction in which a carbon-carbon double bond and a carbon-carbon triple bond are redistributed among two fragments, i.e. an alkene and an alkyne. It is typically catalysed by a metal carbenoid, and proceeds via two four-membered intermediates (metallacyclobutenes). As a low-MW alkene is not released, the reaction is usually driven by formation of a ring.
+ rsc:db
+
+
+
+
+
+
+
+
+ A joining reaction in which a carbon-carbon double bond and a carbon-carbon triple bond in the same molecule are redistributed to give a alkene-substituted cycloalkene. It is typically catalysed by a metal carbenoid, and proceeds via two four-membered intermediates (metallacyclobutanes). The reaction is driven by formation of the ring.
+ ring closing enyne metathesis
+ RXNO
+ RXNO:0000283
+ ring-closing enyne metathesis
+
+
+
+
+ A joining reaction in which a carbon-carbon double bond and a carbon-carbon triple bond in the same molecule are redistributed to give a alkene-substituted cycloalkene. It is typically catalysed by a metal carbenoid, and proceeds via two four-membered intermediates (metallacyclobutanes). The reaction is driven by formation of the ring.
+ rsc:db
+
+
+
+
+
+
+
+
+ A ring-breaking reaction in which two carbon-carbon double bonds are redistributed among two fragments, i.e. an alkene and a cycloalkene. It is typically catalysed by a metal carbenoid, and proceeds via two four-membered intermediates (metallacyclobutanes). The reaction is driven by release of ring strain in the cycloalkene.
+ ring opening metathesis
+ RXNO
+ RXNO:0000284
+ ring-opening metathesis
+
+
+
+
+ A ring-breaking reaction in which two carbon-carbon double bonds are redistributed among two fragments, i.e. an alkene and a cycloalkene. It is typically catalysed by a metal carbenoid, and proceeds via two four-membered intermediates (metallacyclobutanes). The reaction is driven by release of ring strain in the cycloalkene.
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction where an aldehyde or ketone reacts with an allyl halide and zinc to give a homoallylic alcohol.
+ RXNO
+ RXNO:0000285
+ Not to be confused with the Luche reduction (the chemoselective reduction of an enone to an allylic alcohol).
+ Luche reaction
+
+
+
+
+ A carbon-carbon coupling reaction where an aldehyde or ketone reacts with an allyl halide and zinc to give a homoallylic alcohol.
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+ The chemoselective reduction of an enone to give an allylic alcohol, using sodium borohydride and an lanthanoid chloride, typically cerium chloride.
+ RXNO
+ RXNO:0000286
+ Not to be confused with the Luche reaction (the coupling of an aldehyde or ketone with an allyl halide).
+ Luche reduction
+
+
+
+
+ The chemoselective reduction of an enone to give an allylic alcohol, using sodium borohydride and an lanthanoid chloride, typically cerium chloride.
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The oxidation of an aldehyde to a carboxylic acid with chlorite.
+ RXNO
+ RXNO:0000287
+ Lindgren oxidation
+
+
+
+
+ The oxidation of an aldehyde to a carboxylic acid with chlorite.
+ doi:10.3891/acta.chem.scand.27-0888
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction where an aryl halide reacts with copper(I) cyanide to give an aryl nitrile.
+ https://www.rsc.org/Merck-Index/reaction/r376/
+ Rosenmund-von Braun synthesis
+ RXNO
+ RXNO:0000288
+ Rosenmund-von Braun reaction
+
+
+
+
+ A carbon-carbon coupling reaction where an aryl halide reacts with copper(I) cyanide to give an aryl nitrile.
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+ The formation of urea from ammonium cyanate. Ammonium cyanate is unstable, and so is formed in situ from either (a) cyanic acid and ammonia, (b) a metal cyanate and an ammonium salt, or (c) a metal cyanate and ammonia.
+ Woehler synthesis
+ Wohler reaction
+ Wohler synthesis
+ RXNO
+ RXNO:0000289
+ Woehler reaction
+
+
+
+
+ The formation of urea from ammonium cyanate. Ammonium cyanate is unstable, and so is formed in situ from either (a) cyanic acid and ammonia, (b) a metal cyanate and an ammonium salt, or (c) a metal cyanate and ammonia.
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+ The addition of a hydrosilane across the double bond of an alkene or alkyne to give a more substituted silane. Addition to an aldehyde or ketone produces a silyl ether.
+ hydrosilation
+ RXNO
+ RXNO:0000290
+ hydrosilylation
+
+
+
+
+ The addition of a hydrosilane across the double bond of an alkene or alkyne to give a more substituted silane. Addition to an aldehyde or ketone produces a silyl ether.
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+ The addition of the N-H bond of an amine across a double bond of an alkene or alkyne, to give a more substituted amine.
+ RXNO
+ RXNO:0000291
+ hydroamination
+
+
+
+
+ The addition of the N-H bond of an amine across a double bond of an alkene or alkyne, to give a more substituted amine.
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+ The addition of a boron hydride across a double bond of an alkene or alkyne. The boron usually adds to the less substituted carbon.
+ RXNO
+ RXNO:0000292
+ hydroboration
+
+
+
+
+ The addition of a boron hydride across a double bond of an alkene or alkyne. The boron usually adds to the less substituted carbon.
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+ The formal addition of water across a double bond of an alkene or alkyne by formation of an organoborane and in situ oxidation, typically with basic peroxide. The product is usually the less substituted alcohol.
+ RXNO
+ RXNO:0000293
+ hydroboration-oxidation
+
+
+
+
+ The formal addition of water across a double bond of an alkene or alkyne by formation of an organoborane and in situ oxidation, typically with basic peroxide. The product is usually the less substituted alcohol.
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+ The reaction of any of a number of metal hydride species with an alkene or alkyne, to give an intermediate organometal species that can give various products after work-up.
+ hydrometalation
+ RXNO
+ RXNO:0000294
+ hydrometallation
+
+
+
+
+ The reaction of any of a number of metal hydride species with an alkene or alkyne, to give an intermediate organometal species that can give various products after work-up.
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+ The reaction of a organozirconium hydride with an alkene or alkyne, to give an intermediate zirconium species that can give various products after work-up. The zirconium reagent used is typically Schwartz's reagent, Cp2ZrHCl.
+ RXNO
+ RXNO:0000295
+ hydrozirconation
+
+
+
+
+ The reaction of a organozirconium hydride with an alkene or alkyne, to give an intermediate zirconium species that can give various products after work-up. The zirconium reagent used is typically Schwartz's reagent, Cp2ZrHCl.
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+ The reaction of a organotin hydride with an alkene or alkyne, to give an intermediate tin species that can give various products after work-up.
+ RXNO
+ RXNO:0000296
+ hydrostannylation
+
+
+
+
+ The reaction of a organotin hydride with an alkene or alkyne, to give an intermediate tin species that can give various products after work-up.
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+ The reaction of a organotellurium hydride with an alkyne, to give a (usually (Z)-configured) vinyltellurium species.
+ RXNO
+ RXNO:0000297
+ hydrotelluration
+
+
+
+
+ The reaction of a organotellurium hydride with an alkyne, to give a (usually (Z)-configured) vinyltellurium species.
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+ The oxidation of a primary alcohol to an aldehyde or a secondary alcohol to a ketone using Fetizon's reagent.
+ RXNO
+ RXNO:0000298
+ Fetizon oxidation
+
+
+
+
+ The oxidation of a primary alcohol to an aldehyde or a secondary alcohol to a ketone using Fetizon's reagent.
+ :cg
+ rsc:db
+
+
+
+
+
+
+
+
+ The substitution of an acylated sugar with a silylated base to give a nucleoside.
+ Vorbrueggen glycosylation
+ Vorbruggen condensation
+ Vorbruggen glycosylation
+ RXNO
+ RXNO:0000299
+ Vorbrueggen condensation
+
+
+
+
+ The substitution of an acylated sugar with a silylated base to give a nucleoside.
+ :
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+ The addition of a thiol across the double bond of an alkene to give a thioether.
+ thiol-ene click reaction
+ RXNO
+ RXNO:0000300
+ thiol-ene reaction
+
+
+
+
+ The addition of a thiol across the double bond of an alkene to give a thioether.
+ :cg
+ rsc:db
+
+
+
+
+
+
+
+
+ The nickel-catalysed carbon-carbon coupling of a dihaloaromatic compound or aromatic bistriflate to give a polymer.
+ Yamamoto coupling
+ Yamamoto polymerization
+ RXNO
+ RXNO:0000301
+ Yamamoto polymerisation
+
+
+
+
+ The nickel-catalysed carbon-carbon coupling of a dihaloaromatic compound or aromatic bistriflate to give a polymer.
+ https://orcid.org/0000-0002-4077-4719
+ rsc:db
+
+
+
+
+
+
+
+
+ The thermally induced addition of a hydrosilane across the double bond of an alkene or alkyne to give a more substituted silane, usually applied to cases where the hydrosilane is part of a silicon surface.
+ RXNO
+ RXNO:0000302
+ thermal hydrosilylation
+
+
+
+
+ The thermally induced addition of a hydrosilane across the double bond of an alkene or alkyne to give a more substituted silane, usually applied to cases where the hydrosilane is part of a silicon surface.
+ :cg
+ rsc:db
+
+
+
+
+
+
+
+
+ The photochemically induced addition of a hydrosilane across the double bond of an alkene or alkyne to give a more substituted silane, usually applied to cases where the hydrosilane is part of a silicon surface. The reaction uses UV irradiation and is usually initiated by an added photoactive compound such as a platinum catalyst.
+ photo-hydrosilylation
+ RXNO
+ RXNO:0000303
+ photohydrosilylation
+
+
+
+
+ The photochemically induced addition of a hydrosilane across the double bond of an alkene or alkyne to give a more substituted silane, usually applied to cases where the hydrosilane is part of a silicon surface. The reaction uses UV irradiation and is usually initiated by an added photoactive compound such as a platinum catalyst.
+ :cg
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction between a tetrazole sulfone and an aldehyde or ketone to give a (typically trans) alkene.
+ Julia-Kocienski coupling
+ Julia-Kocienski reaction
+ RXNO
+ RXNO:0000304
+ Julia-Kocienski olefination
+
+
+
+
+ A carbon-carbon coupling reaction between a tetrazole sulfone and an aldehyde or ketone to give a (typically trans) alkene.
+ rsc:db
+
+
+
+
+
+
+
+
+ The conversion of a selenoxide with an alpha-hydrogen to an alpha-subtituted selenoether.
+ selenoxide Pummerer reaction
+ RXNO
+ RXNO:0000305
+ seleno-Pummerer rearrangement
+
+
+
+
+ The conversion of a selenoxide with an alpha-hydrogen to an alpha-subtituted selenoether.
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction where an organohalide or triflate couples to an alkene in the same molecule, catalysed by palladium.
+ intramolecular Heck-Mizoroki
+ RXNO
+ RXNO:0000306
+ intramolecular Heck reaction
+
+
+
+
+ A carbon-carbon coupling reaction where an organohalide or triflate couples to an alkene in the same molecule, catalysed by palladium.
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An intramolecular Heck reaction of an ortho-halo-aniline with an alkene, catalysed by palladium.
+ Mori-Ban indole reaction
+ RXNO
+ RXNO:0000307
+ Mori-Ban indole synthesis
+
+
+
+
+ An intramolecular Heck reaction of an ortho-halo-aniline with an alkene, catalysed by palladium.
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The intramolecular esterification of a carboxylic acid group with an alcohol group using 2,4,6-trichlorobenzoyl chloride (Yamaguchi reagent) - an intramolecular Yamaguchi esterification.
+ Yamaguchi lactonization
+ RXNO
+ RXNO:0000308
+ Yamaguchi lactonisation
+
+
+
+
+ The intramolecular esterification of a carboxylic acid group with an alcohol group using 2,4,6-trichlorobenzoyl chloride (Yamaguchi reagent) - an intramolecular Yamaguchi esterification.
+ rsc:db
+
+
+
+
+
+
+
+
+ The esterification of a carboxylic acid with an alcohol using 2,4,6-trichlorobenzoyl chloride (Yamaguchi reagent).
+ https://www.rsc.org/Merck-Index/reaction/r479/
+ RXNO
+ RXNO:0000309
+ Yamaguchi esterification
+
+
+
+
+ The esterification of a carboxylic acid with an alcohol using 2,4,6-trichlorobenzoyl chloride (Yamaguchi reagent).
+ rsc:db
+
+
+
+
+
+
+
+
+ A Diels-Alder reaction between a diene and an aldehyde or ketone to give a six-membered oxygen-containing ring compound.
+ oxa Diels-Alder cycloaddition
+ oxa Diels-Alder reaction
+ oxa-Diels-Alder cycloaddition
+ oxo Diels-Alder cycloaddition
+ oxo Diels-Alder reaction
+ oxo-Diels-Alder cycloaddition
+ oxo-Diels-Alder reaction
+ RXNO
+ RXNO:0000310
+ oxa-Diels-Alder reaction
+
+
+
+
+ A Diels-Alder reaction between a diene and an aldehyde or ketone to give a six-membered oxygen-containing ring compound.
+ rsc:db
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction in which a nucleophile reacts with an allyl acetate, allyl halide, allyl carbonate, allyl carbamate, allyl phosphate, allyl sulfone or allyl nitro compound to give an allyl compound. The reaction is catalsed by Pd(0).
+ Trost allylation
+ RXNO
+ RXNO:0000311
+ Tsuji-Trost reaction
+
+
+
+
+ A carbon-carbon coupling reaction in which a nucleophile reacts with an allyl acetate, allyl halide, allyl carbonate, allyl carbamate, allyl phosphate, allyl sulfone or allyl nitro compound to give an allyl compound. The reaction is catalsed by Pd(0).
+ rsc:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A ring rearrangement reaction where an amine reacts with a 2,5-dialkoxytetrahydrofuran to give a pyrrole.
+ Clauson-Kaas pyrrole synthesis
+ RXNO
+ RXNO:0000312
+ Clauson-Kaas reaction
+
+
+
+
+ A ring rearrangement reaction where an amine reacts with a 2,5-dialkoxytetrahydrofuran to give a pyrrole.
+ http://www.clauson-kaas.com/cgi-files/mdmgfx/file-709-116554-7465.pdf
+
+
+
+
+
+
+
+
+ A [4+2] cycloaddition reaction where a diene (or heterocyclic analogue) reacts with a dienophile to form an unsaturated heterocyclic six-membered ring compound.
+ RXNO
+ RXNO:0000313
+ hetero-Diels-Alder reaction
+
+
+
+
+ A [4+2] cycloaddition reaction where a diene (or heterocyclic analogue) reacts with a dienophile to form an unsaturated heterocyclic six-membered ring compound.
+ rsc:djb
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction that is catalysed by a palladium atom.
+ RXNO
+ RXNO:0000316
+ palladium-catalysed carbon-carbon coupling reaction
+
+
+
+
+ A carbon-carbon coupling reaction that is catalysed by a palladium atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A condensation reaction that results in the production of an ester.
+ NAMERXN:3.6
+ RXNO
+ RXNO:0000317
+ ester condensation reaction
+
+
+
+
+ A condensation reaction that results in the production of an ester.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A deprotection reaction where the reactive centre is an amino nitrogen atom.
+ RXNO
+ RXNO:0000320
+ amino group deprotection
+
+
+
+
+ A deprotection reaction where the reactive centre is an amino nitrogen atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A protection reaction where the reactive centre is an amino nitrogen atom.
+ RXNO
+ RXNO:0000321
+ amino group protection
+
+
+
+
+ A protection reaction where the reactive centre is an amino nitrogen atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An amino group protection where the amino nitrogen atom is protected by reaction with benzylamine.
+ RXNO
+ RXNO:0000322
+ benzylamine protection
+
+
+
+
+ An amino group protection where the amino nitrogen atom is protected by reaction with benzylamine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A protection reaction where the reactive centre is a hydroxyl oxygen atom.
+ RXNO
+ RXNO:0000323
+ hydroxyl group protection
+
+
+
+
+ A protection reaction where the reactive centre is a hydroxyl oxygen atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A hydroxyl group protection where the hydroxyl oxygen atom is protected by formation of a benzyl ether.
+ RXNO
+ RXNO:0000324
+ benzyl ether protection
+
+
+
+
+ A hydroxyl group protection where the hydroxyl oxygen atom is protected by formation of a benzyl ether.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A protection reaction where the reactive centre is a carboxy oxygen.
+ RXNO
+ RXNO:0000325
+ carboxylic acid protection
+
+
+
+
+ A protection reaction where the reactive centre is a carboxy oxygen.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An amino group deprotection reaction where a tertbutoxycarbonyl group is removed in acid conditions.
+ RXNO
+ RXNO:0000326
+ Boc deprotection
+
+
+
+
+ An amino group deprotection reaction where a tertbutoxycarbonyl group is removed in acid conditions.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An amino group deprotection reaction where a benzylamine group is removed by hydrogenation.
+ RXNO
+ RXNO:0000327
+ benzylamine deprotection
+
+
+
+
+ An amino group deprotection reaction where a benzylamine group is removed by hydrogenation.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ A hydroxyl group protection where the hydroxyl oxygen atom is protected by formation of a silyl ether.
+ RXNO
+ RXNO:0000328
+ silyl protection
+
+
+
+
+ A hydroxyl group protection where the hydroxyl oxygen atom is protected by formation of a silyl ether.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An experimental procedure with the aim of producing a portion of a given compound or mixture.
+ RXNO
+ RXNO:0000329
+ planned synthesis
+
+
+
+
+ An experimental procedure with the aim of producing a portion of a given compound or mixture.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A hydroxyl group protection where the hydroxyl oxygen atom is protected by formation of an acetate ester.
+ O-Ac protection
+ RXNO
+ RXNO:0000330
+ acetate protection
+
+
+
+
+ A hydroxyl group protection where the hydroxyl oxygen atom is protected by formation of an acetate ester.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A functional modification step in which one singly-bonded substituent, but not a hydrogen, is replaced by another singly-bonded substituent.
+ RXNO
+ RXNO:0000331
+ substitution step
+
+
+
+
+ A functional modification step in which one singly-bonded substituent, but not a hydrogen, is replaced by another singly-bonded substituent.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A substitution step where one singly-bonded substituent on an aromatic skeleton is replaced by another singly-bonded substituent.
+ RXNO
+ RXNO:0000332
+ aromatic substitution step
+
+
+
+
+ A substitution step where one singly-bonded substituent on an aromatic skeleton is replaced by another singly-bonded substituent.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with a copper(I) halide to form an aromatic halide.
+ RXNO
+ RXNO:0000333
+ Sandmeyer halogenation
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with a copper(I) halide to form an aromatic halide.
+ RSC:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with a copper(II) pseudohalide to form an aromatic pseudohalide.
+ RXNO
+ RXNO:0000334
+ Sandmeyer pseudohalogenation
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with a copper(II) pseudohalide to form an aromatic pseudohalide.
+ RSC:db
+
+
+
+
+
+
+
+
+
+ A functional group modification where a carbonyl oxygen is replaced by an amine.
+ batchelorc
+ 2012-03-22T12:15:29Z
+ NAMERXN:1.2
+ RXNO
+ RXNO:0000335
+ reductive amination
+
+
+
+
+ A functional group modification where a carbonyl oxygen is replaced by an amine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reduction reaction where a nitro group is reduced to an amino group.
+ batchelorc
+ 2012-03-22T12:28:47Z
+ NAMERXN:7.1
+ RXNO
+ RXNO:0000337
+ nitro reduction to amine
+
+
+
+
+ A reduction reaction where a nitro group is reduced to an amino group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reduction process where an amide is transformed into an amine.
+ batchelorc
+ 2012-03-22T12:29:51Z
+ NAMERXN:7.2
+ RXNO
+ RXNO:0000338
+ amide reduction to amine
+
+
+
+
+ A reduction process where an amide is transformed into an amine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A hydrogenation reaction where an alkene is reduced to an alkane.
+ batchelorc
+ 2012-03-22T12:30:40Z
+ NAMERXN:7.6
+ RXNO
+ RXNO:0000339
+ alkene reduction to alkane
+
+
+
+
+ A hydrogenation reaction where an alkene is reduced to an alkane.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An N-alkylation where the reactive centre is an amide nitrogen.
+ batchelorc
+ 2012-03-22T03:07:17Z
+ NAMERXN:1.4
+ RXNO
+ RXNO:0000340
+ amide N-alkylation
+
+
+
+
+ An N-alkylation where the reactive centre is an amide nitrogen.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An N-alkylation where the reactive centre is an aniline nitrogen.
+ batchelorc
+ 2012-03-22T03:07:44Z
+ NAMERXN:1.5
+ RXNO
+ RXNO:0000341
+ aniline N-alkylation
+
+
+
+
+ An N-alkylation where the reactive centre is an aniline nitrogen.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A reduction where a nitrile is replaced by an amine function.
+ batchelorc
+ 2012-03-22T03:12:31Z
+ RXNO
+ RXNO:0000342
+ nitrile reduction to amine
+
+
+
+
+ A reduction where a nitrile is replaced by an amine function.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A reduction reaction where an imine function is replaced by an amine.
+ batchelorc
+ 2012-03-22T03:13:12Z
+ RXNO
+ RXNO:0000343
+ imine reduction to amine
+
+
+
+
+ A reduction reaction where an imine function is replaced by an amine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An alkene oxidation where the carbon-carbon double bond is cleaved.
+ batchelorc
+ 2012-03-22T03:15:25Z
+ NAMERXN:1.6
+ RXNO
+ RXNO:0000344
+ alkene oxidative cleavage
+
+
+
+
+ An alkene oxidation where the carbon-carbon double bond is cleaved.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An N-alkylation reaction where the reactive centre is an azacycle ring nitrogen.
+ batchelorc
+ 2012-03-22T03:22:27Z
+ NAMERXN:1.1
+ RXNO
+ RXNO:0000345
+ heteroaryl N-alkylation
+
+
+
+
+ An N-alkylation reaction where the reactive centre is an azacycle ring nitrogen.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A ring formation reaction where the intended product contains an oxacycle that was not in any of the reactants.
+ batchelorc
+ 2012-03-22T03:24:06Z
+ NAMERXN:4.2
+ RXNO
+ RXNO:0000346
+ oxacycle synthesis
+
+
+
+
+ A ring formation reaction where the intended product contains an oxacycle that was not in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A ring formation reaction where the intended product contains an azacycle that was not in any of the reactants.
+ batchelorc
+ 2012-03-22T03:24:12Z
+ NAMERXN:4.1
+ RXNO
+ RXNO:0000347
+ azacycle synthesis
+
+
+
+
+ A ring formation reaction where the intended product contains an azacycle that was not in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A ring formation reaction where the intended product contains an thiacycle that was not in any of the reactants.
+ batchelorc
+ 2012-03-22T03:24:23Z
+ NAMERXN:4.3
+ RXNO
+ RXNO:0000348
+ thiacycle synthesis
+
+
+
+
+ A ring formation reaction where the intended product contains an thiacycle that was not in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A ring formation reaction where the intended product contains a heterocycle that was not in any of the reactants.
+ batchelorc
+ 2012-03-22T03:24:34Z
+ NAMERXN:4
+ RXNO
+ RXNO:0000349
+ heterocycle synthesis
+
+
+
+
+ A ring formation reaction where the intended product contains a heterocycle that was not in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A hydrogenation reaction where an alkyne is reduced to an alkane.
+ batchelorc
+ 2012-03-22T03:30:01Z
+ NAMERXN:7.7
+ RXNO
+ RXNO:0000350
+ alkyne reduction to alkane
+
+
+
+
+ A hydrogenation reaction where an alkyne is reduced to an alkane.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A hydrogenation reaction where an aryl ring is reduced to a cycloalkyl ring.
+ batchelorc
+ 2012-03-22T03:30:50Z
+ RXNO
+ RXNO:0000351
+ aryl reduction to cycloalkyl
+
+
+
+
+ A hydrogenation reaction where an aryl ring is reduced to a cycloalkyl ring.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A hydrogenation reaction where a heteroaryl is reduced to a saturated heterocycle.
+ batchelorc
+ 2012-03-22T03:31:49Z
+ RXNO
+ RXNO:0000352
+ heteroaryl reduction to saturated heterocycle
+
+
+
+
+ A hydrogenation reaction where a heteroaryl is reduced to a saturated heterocycle.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An alcohol oxidation where the alcohol centre is replaced with a carboxy group.
+ batchelorc
+ 2012-03-22T03:34:20Z
+ RXNO
+ RXNO:0000353
+ alcohol oxidation to carboxylic acid
+
+
+
+
+ An alcohol oxidation where the alcohol centre is replaced with a carboxy group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An oxidation reaction where a carbon centre bonded to the benzene ring is oxidized to a carboxyl group.
+ batchelorc
+ 2012-03-22T03:37:52Z
+ RXNO
+ RXNO:0000354
+ benzylic oxidation
+
+
+
+
+ An oxidation reaction where a carbon centre bonded to the benzene ring is oxidized to a carboxyl group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An oxidation reaction where an allylic C-H bond is replaced by a C=O bond.
+ batchelorc
+ 2012-03-22T03:39:47Z
+ RXNO
+ RXNO:0000355
+ This can be done with, for instance, selenium dioxide.
+ allylic oxidation
+
+
+
+
+ An oxidation reaction where an allylic C-H bond is replaced by a C=O bond.
+ http://www.chemtube3d.com/ox_se_allylic.html
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ An oxidation reaction where an alcohol is oxidized to the corresponding carbonyl compound by a dichromate ion.
+ batchelorc
+ 2012-03-22T03:39:47Z
+ RXNO
+ RXNO:0000356
+ Jones oxidation
+
+
+
+
+ An oxidation reaction where an alcohol is oxidized to the corresponding carbonyl compound by a dichromate ion.
+ http://www.chemtube3d.com/ox_jones_oxidation.html
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An acylation reaction where a nitrogen atom is acylated to form an amide.
+ batchelorc
+ 2012-03-22T03:39:47Z
+ NAMERXN:2.1
+ RXNO
+ RXNO:0000357
+ N-acylation to amide
+
+
+
+
+ An acylation reaction where a nitrogen atom is acylated to form an amide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An acylation reaction where a nitrogen atom is acylated to form a urea.
+ batchelorc
+ 2012-03-22T03:39:47Z
+ NAMERXN:2.3
+ RXNO
+ RXNO:0000358
+ N-acylation to urea
+
+
+
+
+ An acylation reaction where a nitrogen atom is acylated to form a urea.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An N-acylation reaction where a nitrogen centre is acylated to form a carbamate.
+ batchelorc
+ 2012-03-22T04:09:47Z
+ NAMERXN:2.4
+ RXNO
+ RXNO:0000359
+ N-acylation to carbamate
+
+
+
+
+ An N-acylation reaction where a nitrogen centre is acylated to form a carbamate.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An O-acylation reaction where an oxygen centre is acylated to result in an ester.
+ batchelorc
+ 2012-03-22T04:10:47Z
+ NAMERXN:2.6
+ RXNO
+ RXNO:0000360
+ O-acylation to ester
+
+
+
+
+ An O-acylation reaction where an oxygen centre is acylated to result in an ester.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A functional group modification where a nitrile reacts with an alcohol under acid catalysis to form an amidine or ester.
+ RXNO
+ RXNO:0000361
+ Pinner reaction
+
+
+
+
+ A functional group modification where a nitrile reacts with an alcohol under acid catalysis to form an amidine or ester.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An oxidation reaction where a nitrile reacts with an alcohol to form an alkyl imidate.
+ RXNO
+ RXNO:0000362
+ nitrile alcoholysis
+
+
+
+
+ An oxidation reaction where a nitrile reacts with an alcohol to form an alkyl imidate.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A functional group modification where an amide is converted to an imidoyl chloride.
+ batchelorc
+ 2012-03-22T05:04:20Z
+ NAMERXN:9.2
+ RXNO
+ RXNO:0000363
+ amide to imidoyl chloride conversion
+
+
+
+
+ A functional group modification where an amide is converted to an imidoyl chloride.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A functional group modification where an alcohol is converted to a halide.
+ batchelorc
+ 2012-03-22T05:05:15Z
+ NAMERXN:9.1
+ RXNO
+ RXNO:0000364
+ alcohol to halide conversion
+
+
+
+
+ A functional group modification where an alcohol is converted to a halide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A functional group modification where a carboxylic acid is converted to an acid chloride.
+ batchelorc
+ 2012-03-22T05:06:09Z
+ NAMERXN:9.3
+ RXNO
+ RXNO:0000365
+ carboxylic acid to acid chloride conversion
+
+
+
+
+ A functional group modification where a carboxylic acid is converted to an acid chloride.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A functional group modification where a nitrile is transformed into a carboxylic acid.
+ batchelorc
+ 2012-03-22T05:12:32Z
+ NAMERXN:9.4
+ RXNO
+ RXNO:0000366
+ nitrile to acid conversion
+
+
+
+
+ A functional group modification where a nitrile is transformed into a carboxylic acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A functional group modification where a carbonyl compound is converted to an imine.
+ batchelorc
+ 2012-03-22T05:17:03Z
+ NAMERXN:9.6
+ RXNO
+ RXNO:0000367
+ carbonyl compound to imine conversion
+
+
+
+
+ A functional group modification where a carbonyl compound is converted to an imine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Oxidation of an alkene to an allene by heating with formaldehyde, an amine and an inorganic salt.
+ batchelorc
+ 2014-01-08T13:48:00Z
+ Crabbe homologation
+ RXNO
+ RXNO:0000368
+ Crabbé homologation
+
+
+
+
+ Oxidation of an alkene to an allene by heating with formaldehyde, an amine and an inorganic salt.
+ doi:10.1039/c39790000859
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction between an arene and a carbonyl compound (an acylation) or an alkyl compound that can form a carbocation (an alkylation) to form a substituted arene.
+ NAMERXN:3.10
+ RXNO
+ RXNO:0000369
+ Friedel-Crafts reaction
+
+
+
+
+ A carbon-carbon coupling reaction between an arene and a carbonyl compound (an acylation) or an alkyl compound that can form a carbocation (an alkylation) to form a substituted arene.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A functional group modification of a nitrile to a 1H-tetrazole by addition of sodium azide.
+ RXNO
+ RXNO:0000370
+ Demko-Sharpless reaction
+
+
+
+
+ A functional group modification of a nitrile to a 1H-tetrazole by addition of sodium azide.
+ doi:10.1021/jo010635w
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A diazotisation that proceeds by the addition of nitrous acid, nitric acid and water, resulting in a diazonium nitrate salt.
+ https://www.rsc.org/Merck-Index/reaction/r174/
+ RXNO
+ RXNO:0000371
+ Griess reaction
+
+
+
+
+ A diazotisation that proceeds by the addition of nitrous acid, nitric acid and water, resulting in a diazonium nitrate salt.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An N-arylation reaction where the reactive centre is an azacycle ring nitrogen.
+ NAMERXN:1.3
+ RXNO
+ RXNO:0000372
+ heteroaryl N-arylation
+
+
+
+
+ An N-arylation reaction where the reactive centre is an azacycle ring nitrogen.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A planned reaction step in which a covalent bond is formed between the molecular skeleton and a functional group and where the skeletal bond order is unchanged.
+ NAMERXN:10
+ RXNO
+ RXNO:0000373
+ this is not part of David's grand diagram - well spotted Roger
+ functional group addition step
+
+
+
+
+ A planned reaction step in which a covalent bond is formed between the molecular skeleton and a functional group and where the skeletal bond order is unchanged.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ Arylation of an amine or an alcohol with an arylboronic acid, stannane or siloxane in air with a copper acetate catalyst.
+ Chan-Lam reaction
+ Chan-Lam-Evans coupling
+ Chan-Lam-Evans reaction
+ RXNO
+ RXNO:0000374
+ The canonical variant is the N-arylation of an amine with an arylboronic acid.
+ Chan-Lam coupling
+
+
+
+
+ Arylation of an amine or an alcohol with an arylboronic acid, stannane or siloxane in air with a copper acetate catalyst.
+ doi:10.1016/j.tet.2012.06.015
+
+
+
+
+
+
+
+
+
+ true
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ N-methylation of a primary or secondary amine with formic acid and formaldehyde to yield a tertiary amine.
+ Eschweiler-Clarke reaction
+ RXNO
+ RXNO:0000376
+ Eschweiler-Clarke methylation
+
+
+
+
+ N-methylation of a primary or secondary amine with formic acid and formaldehyde to yield a tertiary amine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Coupling of two aromatic rings in the presence of a Lewis acid catalyst.
+ https://www.rsc.org/Merck-Index/reaction/r390/
+ RXNO
+ RXNO:0000377
+ Scholl reaction
+
+
+
+
+ Coupling of two aromatic rings in the presence of a Lewis acid catalyst.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+ Scholl reaction within a single molecule to form a larger ring system.
+ RXNO
+ RXNO:0000378
+ intramolecular Scholl reaction
+
+
+
+
+ Scholl reaction within a single molecule to form a larger ring system.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ Scholl reaction between two aromatic molecules to form a single molecule.
+ RXNO
+ RXNO:0000379
+ intermolecular Scholl reaction
+
+
+
+
+ Scholl reaction between two aromatic molecules to form a single molecule.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of a cyclohexanone with methyl vinyl ketone to form a fused-ring cyclohexenone. It is a Michael reaction followed by an intramolecular aldol condensation.
+ https://www.rsc.org/Merck-Index/reaction/r373/
+ RXNO
+ RXNO:0000380
+ Robinson annulation
+
+
+
+
+ Reaction of a cyclohexanone with methyl vinyl ketone to form a fused-ring cyclohexenone. It is a Michael reaction followed by an intramolecular aldol condensation.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Rearrangement of a beta-amino alcohol to yield a carbonyl compound. In the first step the amine is diazotised by reaction with nitrous acid.
+ https://www.rsc.org/Merck-Index/reaction/r432/
+ RXNO
+ RXNO:0000381
+ Tiffeneau-Demjanov rearrangement
+
+
+
+
+ Rearrangement of a beta-amino alcohol to yield a carbonyl compound. In the first step the amine is diazotised by reaction with nitrous acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ Substitution reaction of a primary amine via deazotisation to yield a mixture of the corresponding primary alcohol and secondary alcohol.
+ https://www.rsc.org/Merck-Index/reaction/r106/
+ RXNO
+ RXNO:0000382
+ TODO: Not *entirely* sure how we classify this. Have given it multiple parentage for the now.
+ Demjanov rearrangement
+
+
+
+
+ Substitution reaction of a primary amine via deazotisation to yield a mixture of the corresponding primary alcohol and secondary alcohol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of an thiol with an alkyne to form an alkenyl sulfide.
+
+ 2021-05-05T09:08:42Z
+ alkyne hydrothiolation
+ RXNO
+ RXNO:0000383
+ thiol-yne reaction
+
+
+
+
+ Reaction of an thiol with an alkyne to form an alkenyl sulfide.
+ https://en.wikipedia.org/wiki/Thiol-yne_reaction
+
+
+
+
+
+
+
+
+
+ Base-catalysed rearrangement of a cyclic alpha-haloketone to the ring-contracted cyclic carboxylic acid.
+ RXNO
+ RXNO:0000384
+ cyclic alpha-haloketone Favorskii rearrangement
+
+
+
+
+ Base-catalysed rearrangement of a cyclic alpha-haloketone to the ring-contracted cyclic carboxylic acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Base-catalysed rearrangement of an alpha-haloketone to a carboxylic acid or ester or amide.
+ RXNO
+ RXNO:0000385
+ Favorskii rearrangement
+
+
+
+
+ Base-catalysed rearrangement of an alpha-haloketone to a carboxylic acid or ester or amide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Favorskii rearrangement of a cyclic alpha-dibromoketone followed by decarboxylation to yield a ring-contracted cyclic ketone.
+ RXNO
+ RXNO:0000386
+ Wallach degradation
+
+
+
+
+ Favorskii rearrangement of a cyclic alpha-dibromoketone followed by decarboxylation to yield a ring-contracted cyclic ketone.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of a carbonyl compound with a dimethyl diazomethyl phosphonate under basic conditions to yield an alkyne.
+ https://www.rsc.org/Merck-Index/reaction/r395/
+ RXNO
+ RXNO:0000387
+ Seyferth-Gilbert homologation
+
+
+
+
+ Reaction of a carbonyl compound with a dimethyl diazomethyl phosphonate under basic conditions to yield an alkyne.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of an aldehyde with a dimethyl diazomethyl phosphonate under basic conditions to yield a terminal alkyne.
+ RXNO
+ RXNO:0000388
+ Seyferth-Gilbert aldehyde homologation
+
+
+
+
+ Reaction of an aldehyde with a dimethyl diazomethyl phosphonate under basic conditions to yield a terminal alkyne.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of a ketone with a dimethyl diazomethyl phosphonate under basic conditions to yield a terminal alkyne.
+ RXNO
+ RXNO:0000389
+ Seyferth-Gilbert ketone homologation
+
+
+
+
+ Reaction of a ketone with a dimethyl diazomethyl phosphonate under basic conditions to yield a terminal alkyne.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Seyferth-Gilbert aldehyde homologation where the Seyferth-Gilbert reagent is generated in situ by reaction with methanol and potassium carbonate.
+ https://www.rsc.org/Merck-Index/reaction/r395/
+ Bestmann modification
+ Ohira-Bestmann homologation
+ Ohira-Bestmann modification
+ RXNO
+ RXNO:0000390
+ Seyferth-Gilbert-Bestmann homologation
+
+
+
+
+ Seyferth-Gilbert aldehyde homologation where the Seyferth-Gilbert reagent is generated in situ by reaction with methanol and potassium carbonate.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ Synthesis of a pyrazole by condensation of a 1,3-dicarbonyl compound with a hydrazine, hydrazide, semicarbazide or aminoguanidine.
+ https://www.rsc.org/Merck-Index/reaction/r233/
+ RXNO
+ RXNO:0000391
+ Knorr pyrazole synthesis
+
+
+
+
+ Synthesis of a pyrazole by condensation of a 1,3-dicarbonyl compound with a hydrazine, hydrazide, semicarbazide or aminoguanidine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which the intended product is a pyrazole that was not present in any of the reactants.
+ RXNO
+ RXNO:0000392
+ pyrazole synthesis
+
+
+
+
+ A reaction in which the intended product is a pyrazole that was not present in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which the intended product is a quinoline that was not present in any of the reactants.
+ RXNO
+ RXNO:0000393
+ quinoline synthesis
+
+
+
+
+ A reaction in which the intended product is a quinoline that was not present in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Synthesis of an alpha-hydroxyquinoline by reaction of a beta-ketoester and an arylamine then dehydration with concentrated sulfuric acid.
+ https://www.rsc.org/Merck-Index/reaction/r234/
+ RXNO
+ RXNO:0000394
+ Knorr quinoline synthesis
+
+
+
+
+ Synthesis of an alpha-hydroxyquinoline by reaction of a beta-ketoester and an arylamine then dehydration with concentrated sulfuric acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which the intended product is an indole that was not present in any of the reactants.
+ RXNO
+ RXNO:0000395
+ indole synthesis
+
+
+
+
+ A reaction in which the intended product is an indole that was not present in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Palladium-catalysed synthesis of a 2,3-substituted indole by reaction of an ortho-iodoaniline with an internal alkyne.
+ https://www.rsc.org/Merck-Index/reaction/r250/
+ Larock indolisation
+ Larock indolization
+ RXNO
+ RXNO:0000396
+ Larock indole synthesis
+
+
+
+
+ Palladium-catalysed synthesis of a 2,3-substituted indole by reaction of an ortho-iodoaniline with an internal alkyne.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of an organic diazo compound with an acetylene to yield a pyrazole.
+ https://www.rsc.org/Merck-Index/reaction/r323/
+ RXNO
+ RXNO:0000397
+ Pechmann pyrazole synthesis
+
+
+
+
+ Reaction of an organic diazo compound with an acetylene to yield a pyrazole.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which the intended product is a benzimidazole that was not present in any of the reactants.
+ RXNO
+ RXNO:0000398
+ benzimidazole synthesis
+
+
+
+
+ A reaction in which the intended product is a benzimidazole that was not present in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of an ortho-diaminobenzene with a carboxylic acid under heat to yield a benzimidazole.
+ Phillips benzimidazole condensation
+ RXNO
+ RXNO:0000399
+ This may be done in the presence of an acid, hexamethyldisilazane in the presence of catalytic triflic acid, a titanium catalyst, elevated pressure, or under UV. [ISBN:9780080534459]
+ Phillips benzimidazole synthesis
+
+
+
+
+ Reaction of an ortho-diaminobenzene with a carboxylic acid under heat to yield a benzimidazole.
+ ISBN:9780080534459
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which the intended product is a pyrimidine that was not present in any of the reactants.
+ RXNO
+ RXNO:0000400
+ pyrimidine synthesis
+
+
+
+
+ A reaction in which the intended product is a pyrimidine that was not present in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which the intended product is a triazine that was not present in any of the reactants.
+ RXNO
+ RXNO:0000401
+ triazine synthesis
+
+
+
+
+ A reaction in which the intended product is a triazine that was not present in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of a 1,3-dicarbonyl compound with an amidine to yield a pyrimidine.
+ RXNO
+ RXNO:0000402
+ Pinner pyrimidine synthesis
+
+
+
+
+ Reaction of a 1,3-dicarbonyl compound with an amidine to yield a pyrimidine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of aryl amidines or halogenated aliphatics amidines with phosgene to yield a 2-hydroxy-4,6-diaryl-s-triazine with loss of ammonia.
+ https://www.rsc.org/Merck-Index/reaction/r343/
+ RXNO
+ RXNO:0000403
+ Pinner triazine synthesis
+
+
+
+
+ Reaction of aryl amidines or halogenated aliphatics amidines with phosgene to yield a 2-hydroxy-4,6-diaryl-s-triazine with loss of ammonia.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Cyclisation-condensation of a beta-arylethanol with an aldehyde to yield an ortho,peri-fused aryl-oxacycle.
+ RXNO
+ RXNO:0000404
+ oxa-Pictet-Spengler reaction
+
+
+
+
+ Cyclisation-condensation of a beta-arylethanol with an aldehyde to yield an ortho,peri-fused aryl-oxacycle.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Epoxidation of an alkene by reaction with a peroxy acid.
+ https://www.rsc.org/Merck-Index/reaction/r351/
+ Prileschajew reaction
+ Prilezhaev reaction
+ RXNO
+ RXNO:0000405
+ Prilezhaev epoxidation
+
+
+
+
+ Epoxidation of an alkene by reaction with a peroxy acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Conversion of an alcohol to an alkyl halide with triphenylphosphine and a halide source.
+ Appel reaction
+ RXNO
+ RXNO:0000406
+ Appel halogenation
+
+
+
+
+ Conversion of an alcohol to an alkyl halide with triphenylphosphine and a halide source.
+ doi:10.1002/anie.197508011
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Conversion of an alcohol to an alkyl iodide with triphenylphosphine and tetraiodomethane.
+ RXNO
+ RXNO:0000407
+ Appel iodination
+
+
+
+
+ Conversion of an alcohol to an alkyl iodide with triphenylphosphine and tetraiodomethane.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Conversion of an alcohol to an alkyl chloride with triphenylphosphine and tetrachloromethane.
+ RXNO
+ RXNO:0000408
+ Appel chlorination
+
+
+
+
+ Conversion of an alcohol to an alkyl chloride with triphenylphosphine and tetrachloromethane.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Conversion of an alcohol to an alkyl bromide with triphenylphosphine and tetrabromomethane or bromine.
+ RXNO
+ RXNO:0000409
+ Appel bromination
+
+
+
+
+ Conversion of an alcohol to an alkyl bromide with triphenylphosphine and tetrabromomethane or bromine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Rearrangement of a primary carboxylic amide to an isocyanate.
+ RXNO
+ RXNO:0000410
+ This counts as an end-of-chain chain shortening because the terminal carbon is separated from the skeleton into the isocyanate group.
+ Hofmann rearrangement
+
+
+
+
+ Rearrangement of a primary carboxylic amide to an isocyanate.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Conversion of a primary carboxylic amide to the lower homologue primary amine. The first step is the Hofmann rearrangement
+ https://www.rsc.org/Merck-Index/reaction/r209/
+ RXNO
+ Hofmann degradation
+ RXNO:0000411
+ Hofmann reaction
+
+
+
+
+ Conversion of a primary carboxylic amide to the lower homologue primary amine. The first step is the Hofmann rearrangement
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Rearrangement of an O-aryl thiocarbamate to an S-aryl thiocarbamate by migration of the aryl group.
+ https://www.wikidata.org/wiki/Q909753
+ RXNO
+ RXNO:0000412
+ Newman-Kwart rearrangement
+
+
+
+
+ Rearrangement of an O-aryl thiocarbamate to an S-aryl thiocarbamate by migration of the aryl group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ Substitution of phenol ortho- or para-bromo or iodo groups by a nitro group on treatment with nitrous acid or a nitrite in acetic acid.
+ https://www.rsc.org/Merck-Index/reaction/r484/
+ https://www.wikidata.org/wiki/Q1061336
+ RXNO
+ RXNO:0000413
+ Zincke nitration
+
+
+
+
+ Substitution of phenol ortho- or para-bromo or iodo groups by a nitro group on treatment with nitrous acid or a nitrite in acetic acid.
+ https://www.rsc.org/Merck-Index/reaction/r484/
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A coupling of an aldehyde with an alpha-haloethanoate ester to form the next homologous aldehyde.
+ RXNO
+ RXNO:0000414
+ These are not necessary-and-sufficient conditions because we can't say "one longer" in OWL.
+ haloethanoate ester-aldehyde Darzens reaction
+
+
+
+
+ A coupling of an aldehyde with an alpha-haloethanoate ester to form the next homologous aldehyde.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A coupling of a ketone with an alpha-haloethanoate ester to replace the oxo group with a formyl group.
+ RXNO
+ RXNO:0000415
+ haloethanoate ester-ketone Darzens reaction
+
+
+
+
+ A coupling of a ketone with an alpha-haloethanoate ester to replace the oxo group with a formyl group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Protection of a primary amino group by reaction with phthalic anhydride.
+ RXNO
+ RXNO:0000418
+ phthalimide protection
+
+
+
+
+ Protection of a primary amino group by reaction with phthalic anhydride.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Conversion of a phthalimide into the corresponding primary amine.
+ RXNO
+ RXNO:0000419
+ phthalimide deprotection
+
+
+
+
+ Conversion of a phthalimide into the corresponding primary amine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Condensation of a 1,5-diketone with ammonium acetate in acetic acid to form a pyridine.
+ http://dx.doi.org/10.1039/SP543
+ https://www.wikidata.org/wiki/Q2144364
+ Krohnke pyridine synthesis
+ RXNO
+ RXNO:0000420
+ Kröhnke pyridine synthesis
+
+
+
+
+ Condensation of a 1,5-diketone with ammonium acetate in acetic acid to form a pyridine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A Gattermann halogenation where the aryl diazonium salt reacts with copper powder and hydrochloric acid to yield an aromatic chloride.
+ RXNO
+ RXNO:0000421
+ Gattermann chlorination
+
+
+
+
+ A Gattermann halogenation where the aryl diazonium salt reacts with copper powder and hydrochloric acid to yield an aromatic chloride.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A Gattermann halogenation where the aryl diazonium salt reacts with copper powder and hydrobromic acid to yield an aromatic bromide.
+ RXNO
+ RXNO:0000422
+ Gattermann bromination
+
+
+
+
+ A Gattermann halogenation where the aryl diazonium salt reacts with copper powder and hydrobromic acid to yield an aromatic bromide.
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A joining reaction between an aldehyde and an alkyl halide or aryl halide or vinyl halide or allyl halide in the presence of metal to give a secondary alcohol.
+ RXNO
+ RXNO:0000426
+ aldehyde Barbier reaction
+
+
+
+
+ A joining reaction between an aldehyde and an alkyl halide or aryl halide or vinyl halide or allyl halide in the presence of metal to give a secondary alcohol.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A joining reaction between an ketone and an alkyl halide or aryl halide or vinyl halide or allyl halide in the presence of metal to give a tertiary alcohol.
+ RXNO
+ RXNO:0000427
+ ketone Barbier reaction
+
+
+
+
+ A joining reaction between an ketone and an alkyl halide or aryl halide or vinyl halide or allyl halide in the presence of metal to give a tertiary alcohol.
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Protection of a hydroxy group by reaction with pivaloyl chloride, resulting in formation of a pivaloyl ester.
+ RXNO
+ RXNO:0000428
+ pivaloyl protection
+
+
+
+
+ Protection of a hydroxy group by reaction with pivaloyl chloride, resulting in formation of a pivaloyl ester.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A hydroxy group deprotection where a pivalate group is removed in acid or base conditions.
+ RXNO
+ RXNO:0000429
+ pivaloyl deprotection
+
+
+
+
+ A hydroxy group deprotection where a pivalate group is removed in acid or base conditions.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A deprotection reaction where the reactive centre is an oxygen atom.
+ alcohol deprotection
+ RXNO
+ RXNO:0000430
+ hydroxy group deprotection
+
+
+
+
+ A deprotection reaction where the reactive centre is an oxygen atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carboxylic acid reduction where the product is the corresponding primary alcohol.
+ RXNO
+ RXNO:0000431
+ carboxylic acid to primary alcohol reduction
+
+
+
+
+ A carboxylic acid reduction where the product is the corresponding primary alcohol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carboxy group protection where the product is a tert-butyl ester.
+ RXNO
+ RXNO:0000432
+ tert-butyl protection
+
+
+
+
+ A carboxy group protection where the product is a tert-butyl ester.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A deprotection reaction where the reactive centre is a carboxy oxygen atom.
+ RXNO
+ RXNO:0000433
+ carboxy group deprotection
+
+
+
+
+ A deprotection reaction where the reactive centre is a carboxy oxygen atom.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A deprotection reaction where the reactant is a tert-butyl ester and the product is a carboxylic acid.
+ RXNO
+ RXNO:0000434
+ tert-butyl ester deprotection
+
+
+
+
+ A deprotection reaction where the reactant is a tert-butyl ester and the product is a carboxylic acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A deprotection reaction where the reactant is a methyl ester and the product is a carboxylic acid.
+ RXNO
+ RXNO:0000435
+ methyl ester deprotection
+
+
+
+
+ A deprotection reaction where the reactant is a methyl ester and the product is a carboxylic acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A deprotection reaction where the reactant is an ethyl ester and the product is a carboxylic acid.
+ RXNO
+ RXNO:0000436
+ ethyl ester deprotection
+
+
+
+
+ A deprotection reaction where the reactant is an ethyl ester and the product is a carboxylic acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An objective specification that describes how a molecule's skeleton and substituents are to be transformed by a given experiment.
+ RXNO
+ RXNO:0000437
+ molecular transformation objective
+
+
+
+
+ An objective specification that describes how a molecule's skeleton and substituents are to be transformed by a given experiment.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A molecular transformation specification that specifies that atoms should be lost from the molecular skeleton.
+ RXNO
+ RXNO:0000438
+ molecular skeleton cleaving objective
+
+
+
+
+ A molecular transformation specification that specifies that atoms should be lost from the molecular skeleton.
+ RSC:db
+
+
+
+
+
+
+
+
+ A molecular transformation specification that specifies that the product should contain a ring that was not in any of the reactants.
+ RXNO
+ RXNO:0000439
+ molecular ring formation objective
+
+
+
+
+ A molecular transformation specification that specifies that the product should contain a ring that was not in any of the reactants.
+ RSC:db
+
+
+
+
+
+
+
+
+ A molecular transformation specification that specifies that atoms should be added to the molecular skeleton.
+ RXNO
+ RXNO:0000440
+ molecular skeleton joining objective
+
+
+
+
+ A molecular transformation specification that specifies that atoms should be added to the molecular skeleton.
+ RSC:db
+
+
+
+
+
+
+
+
+ A molecular transformation specification that specifies that the number of rings and number of skeletal atoms should be preserved and that one or more atoms or groups of atoms move from one atom to another.
+ RXNO
+ RXNO:0000441
+ molecular rearrangement objective
+
+
+
+
+ A molecular transformation specification that specifies that the number of rings and number of skeletal atoms should be preserved and that one or more atoms or groups of atoms move from one atom to another.
+ RSC:db
+
+
+
+
+
+
+
+
+ A molecular transformation specification that specifies that the substituents of a molecule should be changed but the number of atoms in the skeleton and their connectivity, but not necessarily the bond orders, should remain the same.
+ RXNO
+ RXNO:0000442
+ functional modification objective
+
+
+
+
+ A molecular transformation specification that specifies that the substituents of a molecule should be changed but the number of atoms in the skeleton and their connectivity, but not necessarily the bond orders, should remain the same.
+ RSC:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of allyltrimethylsilane with a carbon electrophile to allylate the carbon electrophile.
+ https://www.rsc.org/Merck-Index/reaction/r383/
+ https://www.wikidata.org/wiki/Q903031
+ Hosomi-Sakurai reaction
+ RXNO
+ RXNO:0000443
+ Sakurai reaction
+
+
+
+
+ Reaction of allyltrimethylsilane with a carbon electrophile to allylate the carbon electrophile.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Rearrangement of the acyl group in a phenolate ester to the ortho- and/or para-position. It is catalysed by a Lewis acid.
+ https://www.rsc.org/Merck-Index/reaction/r160/
+ https://www.wikidata.org/wiki/Q574893
+ photo-Fries rearrangement
+ RXNO
+ RXNO:0000444
+ Can be promoted by heat or UV. The UV version (photo-Fries) involves a radical mechanism.
+ Fries rearrangement
+
+
+
+
+ Rearrangement of the acyl group in a phenolate ester to the ortho- and/or para-position. It is catalysed by a Lewis acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Rearrangement of the acyl group in a phenolate ester to the ortho-position.
+ RXNO
+ RXNO:0000445
+ ortho-Fries rearrangement
+
+
+
+
+ Rearrangement of the acyl group in a phenolate ester to the ortho-position.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Rearrangement of the acyl group in a phenolate ester to the para-position.
+ RXNO
+ RXNO:0000446
+ para-Fries rearrangement
+
+
+
+
+ Rearrangement of the acyl group in a phenolate ester to the para-position.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Formylation of a phenol or aromatic amine with hexamethylenetetramine in acidic conditions.
+ https://www.rsc.org/Merck-Index/reaction/r119/
+ https://www.wikidata.org/wiki/Q903217
+ RXNO
+ RXNO:0000447
+ Duff reaction
+
+
+
+
+ Formylation of a phenol or aromatic amine with hexamethylenetetramine in acidic conditions.
+ https://doi.org/10.1039/JR9450000276
+ https://doi.org/10.1039/jr9410000547
+
+
+
+
+
+
+
+
+ A molecular skeleton joining adjective that is satisfied by a chain part of a molecular skeleton being lengthened.
+ RXNO
+ RXNO:0000448
+ molecular chain lengthening objective
+
+
+
+
+ A molecular skeleton joining adjective that is satisfied by a chain part of a molecular skeleton being lengthened.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A molecular skeleton transformation objective that is satisfied by a reaction where the product has fewer rings than the reactants.
+ RXNO
+ RXNO:0000449
+ molecular ring breaking objective
+
+
+
+
+ A molecular skeleton transformation objective that is satisfied by a reaction where the product has fewer rings than the reactants.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A molecular skeleton transformation objective that is satisfied by a reaction where an existing ring is reduced in size.
+ RXNO
+ RXNO:0000450
+ molecular ring contraction objective
+
+
+
+
+ A molecular skeleton transformation objective that is satisfied by a reaction where an existing ring is reduced in size.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction in which an aldehyde reacts with allyltrimethylsilane to form a homoallylic alcohol.
+ RXNO
+ RXNO:0000451
+ aldehyde Sakurai reaction
+
+
+
+
+ A carbon-carbon coupling reaction in which an aldehyde reacts with allyltrimethylsilane to form a homoallylic alcohol.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction in which a ketone reacts with allyltrimethylsilane to form a homoallylic alcohol.
+ RXNO
+ RXNO:0000452
+ ketone Sakurai reaction
+
+
+
+
+ A carbon-carbon coupling reaction in which a ketone reacts with allyltrimethylsilane to form a homoallylic alcohol.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A molecular skeleton transformation objective that is satisfied by a reaction in which a functional group undergoes a change that does not affect the number of atoms in (or connectivity of) the skeleton of the molecule.
+ RXNO
+ RXNO:0000453
+ functional group modification objective
+
+
+
+
+ A molecular skeleton transformation objective that is satisfied by a reaction in which a functional group undergoes a change that does not affect the number of atoms in (or connectivity of) the skeleton of the molecule.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A molecular skeleton transformation objective that is satisfied by a reaction in which a single skeletal atom is removed from the end of a chain.
+ RXNO
+ RXNO:0000454
+ end-of-chain chain shortening objective
+
+
+
+
+ A molecular skeleton transformation objective that is satisfied by a reaction in which a single skeletal atom is removed from the end of a chain.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A functional group modification objective that is satisfied by a reaction in which a functional group is reduced.
+ RXNO
+ RXNO:0000455
+ functional reduction objective
+
+
+
+
+ A functional group modification objective that is satisfied by a reaction in which a functional group is reduced.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A functional modification objective that is satisfied by a reaction in which two or more groups of atoms are added to the molecule, resulting in a change of skeletal bond order.
+ RXNO
+ RXNO:0000456
+ addition objective
+
+
+
+
+ A functional modification objective that is satisfied by a reaction in which two or more groups of atoms are added to the molecule, resulting in a change of skeletal bond order.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A molecular transformation objective that is satisfied by a reaction in which an existing skeletal ring is increased in size.
+ RXNO
+ RXNO:0000457
+ molecular ring expansion objective
+
+
+
+
+ A molecular transformation objective that is satisfied by a reaction in which an existing skeletal ring is increased in size.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A molecular transformation objective that is satisfied by a reaction in which the number of skeletal rings in a molecule stays the same but the connectivity of the atoms in at least one ring changes.
+ RXNO
+ RXNO:0000458
+ molecular ring rearrangement objective
+
+
+
+
+ A molecular transformation objective that is satisfied by a reaction in which the number of skeletal rings in a molecule stays the same but the connectivity of the atoms in at least one ring changes.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction between a beta-ketoester and an alkyl halide to yield an alpha-alkylated ester.
+ https://www.rsc.org/Merck-Index/reaction/r1/
+ https://www.wikidata.org/wiki/Q1017086
+ RXNO
+ RXNO:0000459
+ Subsequent treatment with mild hydrolysis leads to a ketone; concentrated base produces a substituted ester.
+ acetoacetic ester synthesis
+
+
+
+
+ A carbon-carbon coupling reaction between a beta-ketoester and an alkyl halide to yield an alpha-alkylated ester.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reductive coupling reaction between two ester groups in the same molecule to give an acyloin (an alpha-hydroxyketone).
+ RXNO
+ RXNO:0000460
+ intramolecular acyloin condensation
+
+
+
+
+ A reductive coupling reaction between two ester groups in the same molecule to give an acyloin (an alpha-hydroxyketone).
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reductive coupling reaction between two ester groups in different molecules to give an acyloin (an alpha-hydroxyketone).
+ RXNO
+ RXNO:0000461
+ intermolecular acyloin condensation
+
+
+
+
+ A reductive coupling reaction between two ester groups in different molecules to give an acyloin (an alpha-hydroxyketone).
+ RSC:db
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+ A molecular transformation objective that is satisfied by a cleaving reaction in which a skeletal atom or group of atoms is removed from the middle of a molecule.
+ RXNO
+ RXNO:0000462
+ molecular extrusion objective
+
+
+
+
+ A molecular transformation objective that is satisfied by a cleaving reaction in which a skeletal atom or group of atoms is removed from the middle of a molecule.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A molecular transformation objective that is satisfied by a reaction in which the parent molecule breaks up into three or more products.
+ RXNO
+ RXNO:0000463
+ molecular fragmentation objective
+
+
+
+
+ A molecular transformation objective that is satisfied by a reaction in which the parent molecule breaks up into three or more products.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A [2+2+1] cycloaddition between an alkyne, an alkene and carbon monoxide to form an alpha-beta-unsaturated cyclopentenone.
+ https://www.rsc.org/Merck-Index/reaction/r320/
+ https://www.wikidata.org/wiki/Q903694
+ RXNO
+ RXNO:0000464
+ Pauson-Khand reaction
+
+
+
+
+ A [2+2+1] cycloaddition between an alkyne, an alkene and carbon monoxide to form an alpha-beta-unsaturated cyclopentenone.
+ doi:10.1039/P19730000975
+
+
+
+
+
+
+
+
+ A molecular transformation objective that is satisfied by a reaction in which a fused ring system is present in a product that was not present in any of the reactants.
+ RXNO
+ RXNO:0000465
+ fused-ring-system formation objective
+
+
+
+
+ A molecular transformation objective that is satisfied by a reaction in which a fused ring system is present in a product that was not present in any of the reactants.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A molecular transformation objective that is satisfied by a reaction in which a large number of monomers react together to product a polymer consisting of repeating units.
+ RXNO
+ RXNO:0000466
+ polymerisation objective
+
+
+
+
+ A molecular transformation objective that is satisfied by a reaction in which a large number of monomers react together to product a polymer consisting of repeating units.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A fused-ring-system formation reaction where a flavonol is produced by oxidation of a chalcone with alkaline hydrogen peroxide.
+ https://www.rsc.org/Merck-Index/reaction/r5/
+ https://www.wikidata.org/wiki/Q903717
+ RXNO
+ RXNO:0000467
+ definition source Merck Index
+ Algar-Flynn-Oyamada reaction
+
+
+
+
+ A fused-ring-system formation reaction where a flavonol is produced by oxidation of a chalcone with alkaline hydrogen peroxide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A molecular transformation objective that is satisfied by a reaction in which one singly-bonded substituent, but not a hydrogen, is replaced by another singly-bonded substituent.
+ RXNO
+ RXNO:0000468
+ molecular substitution objective
+
+
+
+
+ A molecular transformation objective that is satisfied by a reaction in which one singly-bonded substituent, but not a hydrogen, is replaced by another singly-bonded substituent.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of ortho-hydroxyaryl ketones with aromatic carboxylic acid anhydrides to yield a flavone.
+ RXNO
+ RXNO:0000470
+ Allan-Robinson flavone synthesis
+
+
+
+
+ Reaction of ortho-hydroxyaryl ketones with aromatic carboxylic acid anhydrides to yield a flavone.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of ortho-hydroxyaryl ketones with aromatic carboxylic acid anhydrides to yield an isoflavone.
+ RXNO
+ RXNO:0000471
+ Allan-Robinson isoflavone synthesis
+
+
+
+
+ Reaction of ortho-hydroxyaryl ketones with aromatic carboxylic acid anhydrides to yield an isoflavone.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Rearrangement of an aldose N-glycoside to a ketose N-glycoside by acid or base catalysis.
+ https://www.rsc.org/Merck-Index/reaction/r8/
+ https://www.wikidata.org/wiki/Q452196
+ RXNO
+ RXNO:0000472
+ definition source Merck Index
+ Amadori rearrangement
+
+
+
+
+ Rearrangement of an aldose N-glycoside to a ketose N-glycoside by acid or base catalysis.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of a ketone with ethoxyacetylene to form an alkoxyethynyl alcohol.
+ https://www.rsc.org/Merck-Index/reaction/r9/
+ https://www.wikidata.org/wiki/Q16624458
+ RXNO
+ RXNO:0000473
+ Arens-van Dorp synthesis
+
+
+
+
+ Reaction of a ketone with ethoxyacetylene to form an alkoxyethynyl alcohol.
+ https://orcid.org/0000-0001-5985-7429
+ https://www.rsc.org/Merck-Index/reaction/r9/
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Ring expansion of a 2-bromo-2-(alpha-bromobenzyl)-1-benzofuran to a flavonol in alcoholic alkali.
+ https://www.rsc.org/Merck-Index/reaction/r11/
+ https://www.wikidata.org/wiki/Q3115850
+ RXNO
+ RXNO:0000474
+ Auwers synthesis
+
+
+
+
+ Ring expansion of a 2-bromo-2-(alpha-bromobenzyl)-1-benzofuran to a flavonol in alcoholic alkali.
+ https://orcid.org/0000-0001-5985-7429
+ https://www.rsc.org/Merck-Index/reaction/r11/
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of ortho-hydroxyaryl ketones with aromatic acid anhydrides to yield a flavone or isoflavone.
+ https://www.rsc.org/Merck-Index/reaction/r6/
+ https://www.wikidata.org/wiki/Q3046015
+ RXNO
+ RXNO:0000475
+ Allan-Robinson reaction
+
+
+
+
+ Reaction of ortho-hydroxyaryl ketones with aromatic acid anhydrides to yield a flavone or isoflavone.
+ https://orcid.org/0000-0001-5985-7429
+ https://www.rsc.org/Merck-Index/reaction/r6/
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Rearrangement of a propargyl alcohol to an alpha,beta-unsaturated carbonyl compound via an allene intermediate to yield the gamma-substituted product.
+ https://www.rsc.org/Merck-Index/reaction/r278/
+ https://www.wikidata.org/wiki/Q902668
+ RXNO
+ RXNO:0000476
+ Meyer-Schuster rearrangement
+
+
+
+
+ Rearrangement of a propargyl alcohol to an alpha,beta-unsaturated carbonyl compound via an allene intermediate to yield the gamma-substituted product.
+ https://doi.org/10.1039/b912099h
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Rearrangement of a propargyl alcohol to an alpha,beta-unsaturated carbonyl compound via an enyne intermediate to yield the beta-substituted product.
+ https://www.rsc.org/Merck-Index/reaction/r278/
+ RXNO
+ RXNO:0000477
+ Rupe rearrangement
+
+
+
+
+ Rearrangement of a propargyl alcohol to an alpha,beta-unsaturated carbonyl compound via an enyne intermediate to yield the beta-substituted product.
+ https://doi.org/10.1039/b912099h
+
+
+
+
+
+
+
+
+ A Horner-Wadsworth-Emmons reaction that uses phosphonates with electron-withdrawing groups and dissociating conditions to produce predominantly Z-olefins.
+ Still modification
+ RXNO
+ RXNO:0000478
+ Still-Gennari modification
+
+
+
+
+ A Horner-Wadsworth-Emmons reaction that uses phosphonates with electron-withdrawing groups and dissociating conditions to produce predominantly Z-olefins.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A molecular skeleton joining reaction where the connection formed is a carbon-carbon double bond.
+ RXNO
+ RXNO:0000479
+ olefination
+
+
+
+
+ A molecular skeleton joining reaction where the connection formed is a carbon-carbon double bond.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of an aldehyde or ketone or carboxylic ester or amide with the Tebbe reagent to yield an olefin or an enol ether or an enamine.
+ https://www.rsc.org/Merck-Index/reaction/r428/
+ RXNO
+ RXNO:0000480
+ Tebbe olefination
+
+
+
+
+ Reaction of an aldehyde or ketone or carboxylic ester or amide with the Tebbe reagent to yield an olefin or an enol ether or an enamine.
+ https://orcid.org/0000-0001-5985-7429
+ https://www.rsc.org/Merck-Index/reaction/r428/
+
+
+
+
+
+
+
+
+ Cyclization of a enynyl allene to yield a toluene biradical with radical centres on the methyl group and at the meta position.
+ batchelorc
+ 2014-02-28T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r292/
+ https://www.wikidata.org/wiki/Q89925623
+ Myers-Saito cyclization
+ Myers-Saito process
+ Myers-Saito reaction
+ RXNO
+ RXNO:0000481
+ Myers-Saito cyclisation
+
+
+
+
+ Cyclization of a enynyl allene to yield a toluene biradical with radical centres on the methyl group and at the meta position.
+ https://doi.org/10.1039/b009965l
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Cyclization of a enynyl allene to yield a 1-methyl-5-methylenecyclopenta-1,3-diene biradical with radical centres on the methyl group and methylene group.
+ batchelorc
+ 2014-02-28T09:00:00Z
+ Schmittel cyclization
+ RXNO
+ RXNO:0000482
+ Schmittel cyclisation
+
+
+
+
+ Cyclization of a enynyl allene to yield a 1-methyl-5-methylenecyclopenta-1,3-diene biradical with radical centres on the methyl group and methylene group.
+ https://doi.org/10.1039/b009965l
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Copper-catalysed reaction of benzene with a nitrosylating agent and hydrogen peroxide to form an o-nitrosophenol.
+ batchelorc
+ 2014-02-28T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r26/
+ https://www.wikidata.org/wiki/Q3536586
+ RXNO
+ RXNO:0000483
+ Baudisch reaction
+
+
+
+
+ Copper-catalysed reaction of benzene with a nitrosylating agent and hydrogen peroxide to form an o-nitrosophenol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A functional modification objective that is satisfied by deprotecting some functional group.
+ batchelorc
+ 2014-02-28T09:00:00Z
+ RXNO
+ RXNO:0000484
+ deprotection objective
+
+
+
+
+ A functional modification objective that is satisfied by deprotecting some functional group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A functional modification objective that is satisfied by protecting some functional group.
+ batchelorc
+ 2014-02-28T09:00:00Z
+ RXNO
+ RXNO:0000485
+ protection objective
+
+
+
+
+ A functional modification objective that is satisfied by protecting some functional group.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A functional modification objective that is satisfied by a reaction in which two or more groups of atoms are removed from the molecule, resulting in a change of skeletal bond order.
+ batchelorc
+ 2014-02-28T09:00:00Z
+ RXNO
+ RXNO:0000486
+ molecular skeleton elimination objective
+
+
+
+
+ A functional modification objective that is satisfied by a reaction in which two or more groups of atoms are removed from the molecule, resulting in a change of skeletal bond order.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A molecular skeleton joining objective that is satisfied by a reaction in which one or more atoms are added to the middle of a chain.
+ batchelorc
+ 2014-02-28T09:00:00Z
+ RXNO
+ RXNO:0000487
+ molecular skeleton insertion objective
+
+
+
+
+ A molecular skeleton joining objective that is satisfied by a reaction in which one or more atoms are added to the middle of a chain.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A molecular skeleton joining objective that is satisfied by a reaction in which one or more atoms are added to the molecular skeleton and a skeletal rearrangement occurs.
+ batchelorc
+ 2014-02-28T09:00:00Z
+ RXNO
+ RXNO:0000488
+ joining with rearrangement objective
+
+
+
+
+ A molecular skeleton joining objective that is satisfied by a reaction in which one or more atoms are added to the molecular skeleton and a skeletal rearrangement occurs.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A functional modification objective that is satisfied by a reaction in which a covalent bond is formed between the molecular skeleton and a functional group and where the skeletal bond order is unchanged.
+ batchelorc
+ 2014-02-28T09:00:00Z
+ RXNO
+ RXNO:0000489
+ functional group addition objective
+
+
+
+
+ A functional modification objective that is satisfied by a reaction in which a covalent bond is formed between the molecular skeleton and a functional group and where the skeletal bond order is unchanged.
+ RSC:xp
+
+
+
+
+
+
+
+
+ A functional group modification objective that is satisfied by a reaction in which a functional group is oxidised.
+ batchelorc
+ 2014-02-28T09:00:00Z
+ RXNO
+ RXNO:0000490
+ functional oxidation objective
+
+
+
+
+ A functional group modification objective that is satisfied by a reaction in which a functional group is oxidised.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Cyclisation of a propargyl alpha,beta-unsaturated ketone where the reactant rearranges to an allenyl vinyl ketone, followed by a Nazarov cyclisation in which a nucleophile 'intercepts' the intermediate carbocation to yield a cyclopentenone substituted at the alpha position opposite the double bond.
+ batchelorc
+ 2014-02-28T12:00:00Z
+ interrupted Nazarov cyclization
+ RXNO
+ RXNO:0000491
+ interrupted Nazarov cyclisation
+
+
+
+
+ Cyclisation of a propargyl alpha,beta-unsaturated ketone where the reactant rearranges to an allenyl vinyl ketone, followed by a Nazarov cyclisation in which a nucleophile 'intercepts' the intermediate carbocation to yield a cyclopentenone substituted at the alpha position opposite the double bond.
+ doi:10.1039/c3cs60333d
+
+
+
+
+
+
+
+
+ Rearrangement of an N-phenylhydroxamine in acid to yield a para-aminophenol.
+ batchelorc
+ 2014-03-03T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r15/
+ https://www.wikidata.org/wiki/Q139251
+ RXNO
+ RXNO:0000492
+ Bamberger rearrangement
+
+
+
+
+ Rearrangement of an N-phenylhydroxamine in acid to yield a para-aminophenol.
+ https://orcid.org/0000-0001-5985-7429
+ https://www.rsc.org/Merck-Index/reaction/r15/
+
+
+
+
+
+
+
+
+ Reaction of an aromatic diazonium compound with an alkali arsenite in the presence of copper or silver to yield an aromatic arsonic acid.
+ batchelorc
+ 2014-03-03T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r19/
+ RXNO
+ RXNO:0000493
+ Bart reaction
+
+
+
+
+ Reaction of an aromatic diazonium compound with an alkali arsenite in the presence of copper or silver to yield an aromatic arsonic acid.
+ https://orcid.org/0000-0001-5985-7429
+ https://www.rsc.org/Merck-Index/reaction/r19/
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of an ortho-substituted nitroarene with a vinyl Grignard reagent to yield a 7-substituted indole.
+ batchelorc
+ 2014-03-03T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r20/
+ https://www.wikidata.org/wiki/Q3508929
+ RXNO
+ RXNO:0000494
+ Bartoli indole synthesis
+
+
+
+
+ Reaction of an ortho-substituted nitroarene with a vinyl Grignard reagent to yield a 7-substituted indole.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of an aldehyde or ketone with a thioaldehyde or thioketone via a 1,3,4-thiadiazoline intermediate to yield an olefin.
+ batchelorc
+ 2014-03-03T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r23/
+ Barton olefin synthesis
+ RXNO
+ RXNO:0000495
+ Barton olefination
+
+
+
+
+ Reaction of an aldehyde or ketone with a thioaldehyde or thioketone via a 1,3,4-thiadiazoline intermediate to yield an olefin.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of a nitroalkene with an alpha-isocyanoacetate to yield a substituted pyrrole.
+ batchelorc
+ 2014-03-03T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r25/
+ https://www.wikidata.org/wiki/Q4865733
+ Barton-Zard synthesis
+ RXNO
+ RXNO:0000496
+ Barton-Zard reaction
+
+
+
+
+ Reaction of a nitroalkene with an alpha-isocyanoacetate to yield a substituted pyrrole.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction in which the intended product is a pyrrole that was not present in any of the reactants.
+ batchelorc
+ 2014-03-03T09:00:00Z
+ RXNO
+ RXNO:0000497
+ pyrrole synthesis
+
+
+
+
+ A reaction in which the intended product is a pyrrole that was not present in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reduction of an aromatic nitro compound to the corresponding arene by iron in some form in aqueous acid.
+ batchelorc
+ 2014-03-03T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r28/
+ https://www.wikidata.org/wiki/Q906075
+ Bechamp reduction
+ RXNO
+ RXNO:0000498
+ Béchamp reduction
+
+
+
+
+ Reduction of an aromatic nitro compound to the corresponding arene by iron in some form in aqueous acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of a benzofurazan 1-oxide with an enamine or enolate to yield a quinoxaline-1,4-dioxide.
+ batchelorc
+ 2014-03-03T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r30/
+ RXNO
+ RXNO:0000499
+ definition source Merck Index
+ Beirut reaction
+
+
+
+
+ Reaction of a benzofurazan 1-oxide with an enamine or enolate to yield a quinoxaline-1,4-dioxide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of a beta-aminovinylketone with a Grignard reagent to yield a substituted alpha,beta-unsaturated carbonyl compound.
+ batchelorc
+ 2014-03-03T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r31/
+ https://www.wikidata.org/wiki/Q816687
+ Benary reaction
+ RXNO
+ RXNO:0000500
+ Bénary reaction
+
+
+
+
+ Reaction of a beta-aminovinylketone with a Grignard reagent to yield a substituted alpha,beta-unsaturated carbonyl compound.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of an alpha-haloketone or alpha-haloether with a 1,3-dicarbonyl compound in the presence of pyridine to yield a substituted furan.
+ batchelorc
+ 2014-03-03T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r138/
+ https://www.wikidata.org/wiki/Q5441589
+ RXNO
+ RXNO:0000501
+ Feist-Bénary synthesis
+
+
+
+
+ Reaction of an alpha-haloketone or alpha-haloether with a 1,3-dicarbonyl compound in the presence of pyridine to yield a substituted furan.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Rearrangement of a mancude eight-membered system containing a pentacycle into a different pentacycle where two of the ring atoms are ring atoms in the original molecule.
+ batchelorc
+ 2014-03-04T09:00:00Z
+ https://www.wikidata.org/wiki/Q56298381
+ RXNO
+ RXNO:0000502
+ Boulton-Katritzky rearrangement
+
+
+
+
+ Rearrangement of a mancude eight-membered system containing a pentacycle into a different pentacycle where two of the ring atoms are ring atoms in the original molecule.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Rearrangement of an azapentacycle containing a -N= system where there is an unsaturated three-heavy-atom substituent XYZ on the substituent double-bonded to the nitrogen, to a new azapentacycle where the pivotal nitrogen has broken its single bond and formed a new bond with atom Z.
+ batchelorc
+ 2014-03-04T09:00:00Z
+ RXNO
+ RXNO:0000503
+ monocyclic Boulton-Katritzky rearrangement
+
+
+
+
+ Rearrangement of an azapentacycle containing a -N= system where there is an unsaturated three-heavy-atom substituent XYZ on the substituent double-bonded to the nitrogen, to a new azapentacycle where the pivotal nitrogen has broken its single bond and formed a new bond with atom Z.
+ https://doi.org/10.1039/j39670002005
+
+
+
+
+
+
+
+
+ Rearrangement of a mancude bicyclo[4.3.0] compound with an unsaturated two-heavy-atom substituent on the six-membered ring alpha to the bridgehead to form a new mancude bicyclo[4.3.0] compound where the five-membered ring has been formed from the two-heavy-atom substituent and the original five-membered ring has been broken.
+ batchelorc
+ 2014-03-04T09:00:00Z
+ RXNO
+ RXNO:0000504
+ bicyclic Boulton-Katritzky rearrangement
+
+
+
+
+ Rearrangement of a mancude bicyclo[4.3.0] compound with an unsaturated two-heavy-atom substituent on the six-membered ring alpha to the bridgehead to form a new mancude bicyclo[4.3.0] compound where the five-membered ring has been formed from the two-heavy-atom substituent and the original five-membered ring has been broken.
+ https://doi.org/10.1039/j29660001004
+
+
+
+
+
+
+
+
+ Reaction of a primary nitro compound with phenyl isocynatate and triethylamine to yield a nitrile oxide.
+ batchelorc
+ 2014-03-04T09:00:00Z
+ RXNO
+ RXNO:0000505
+ Mukaiyama-Hoshino method
+
+
+
+
+ Reaction of a primary nitro compound with phenyl isocynatate and triethylamine to yield a nitrile oxide.
+ https://doi.org/10.1021/ja01505a017
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of an aldehyde or ketone with a sodium acetylide to yield a propargyl alcohol.
+ batchelorc
+ 2014-03-04T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r298/
+ https://www.wikidata.org/wiki/Q16930708
+ RXNO
+ RXNO:0000506
+ Nef synthesis
+
+
+
+
+ Reaction of an aldehyde or ketone with a sodium acetylide to yield a propargyl alcohol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ Reaction of an ester with an electron-withdrawing group alpha- to the ester functionality with a metal halide or pseudohalide to yield the shorter homologous system.
+ batchelorc
+ 2014-03-04T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r242/
+ https://www.wikidata.org/wiki/Q4597398
+ Krapcho decarbalkoxylation
+ RXNO
+ RXNO:0000507
+ Krapcho decarboxylation
+
+
+
+
+ Reaction of an ester with an electron-withdrawing group alpha- to the ester functionality with a metal halide or pseudohalide to yield the shorter homologous system.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of an aromatic nitro compound with an unsaturated substituent at the alpha-position to form a fused-ring nitrogen heterocycle.
+ batchelorc
+ 2014-03-04T09:00:00Z
+ Cadogan reaction
+ Cadogan ring closure
+ Cadogan ring-closure
+ RXNO
+ RXNO:0000508
+ Cadogan cyclization
+
+
+
+
+ Reaction of an aromatic nitro compound with an unsaturated substituent at the alpha-position to form a fused-ring nitrogen heterocycle.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A Cadogan cyclization that results in an indole.
+ batchelorc
+ 2014-03-05T09:00:00Z
+ RXNO
+ RXNO:0000509
+ Cadogan indole synthesis
+
+
+
+
+ A Cadogan cyclization that results in an indole.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ Addition of hydrogen atoms to unsaturated rings by means of alkali metals in low-molecular weight amines.
+ batchelorc
+ 2014-03-06T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r32/
+ Benkeser reaction
+ RXNO
+ RXNO:0000510
+ Benkeser reduction
+
+
+
+
+ Addition of hydrogen atoms to unsaturated rings by means of alkali metals in low-molecular weight amines.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of an N-(2-alkylphenyl)alkanamide with strong base to form an indole.
+ batchelorc
+ 2014-03-07T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r261/
+ https://www.wikidata.org/wiki/Q2632831
+ Madelung synthesis
+ RXNO
+ RXNO:0000511
+ Madelung indole synthesis
+
+
+
+
+ Reaction of an N-(2-alkylphenyl)alkanamide with strong base to form an indole.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of a N-(2-alkylphenyl)-trimethylsilylamine with two equivalents of organolithium and an ester or carboxylic acid to form an indole.
+ batchelorc
+ 2014-03-07T09:00:00Z
+ Smith-modified Madelung synthesis
+ RXNO
+ RXNO:0000512
+ Smith indole synthesis
+
+
+
+
+ Reaction of a N-(2-alkylphenyl)-trimethylsilylamine with two equivalents of organolithium and an ester or carboxylic acid to form an indole.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Rearrangement of an acyl imidate to form a carboximide.
+ batchelorc
+ 2014-03-07T09:00:00Z
+ https://www.wikidata.org/wiki/Q723311
+ RXNO
+ RXNO:0000513
+ Mumm rearrangement
+
+
+
+
+ Rearrangement of an acyl imidate to form a carboximide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Rearrangement of an aryl imino ether to yield an N,N-diaryl amide.
+ batchelorc
+ 2014-03-07T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r74/
+ RXNO
+ RXNO:0000514
+ Chapman rearrangement
+
+
+
+
+ Rearrangement of an aryl imino ether to yield an N,N-diaryl amide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of an acetylated amino acid with an aldehyde then with a second amino acid, then hydrogenation and hydrolysis to form a dipeptide. It proceeds via an azlactone intermediate.
+ batchelorc
+ 2014-03-10T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r38/
+ RXNO
+ RXNO:0000515
+ Bergmann azlactone peptide synthesis
+
+
+
+
+ Reaction of an acetylated amino acid with an aldehyde then with a second amino acid, then hydrogenation and hydrolysis to form a dipeptide. It proceeds via an azlactone intermediate.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Removal of a terminal amino acid residue from a peptide by benzoylation, azidation, treatment with benzyl alcohol, hydrogenation and hydrolysis.
+ batchelorc
+ 2014-03-11T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r39/
+ RXNO
+ RXNO:0000516
+ Bergmann degradation
+
+
+
+
+ Removal of a terminal amino acid residue from a peptide by benzoylation, azidation, treatment with benzyl alcohol, hydrogenation and hydrolysis.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Removal of a terminal amino acid residue from a peptide.
+ batchelorc
+ 2014-03-11T09:00:00Z
+ RXNO
+ RXNO:0000517
+ terminal amino-acid residue cleaving reaction
+
+
+
+
+ Removal of a terminal amino acid residue from a peptide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Ring formation reaction where the intended product is an acridine.
+ batchelorc
+ 2014-03-12T09:00:00Z
+ RXNO
+ RXNO:0000518
+ acridine synthesis
+
+
+
+
+ Ring formation reaction where the intended product is an acridine.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of a diarylamine in an organic acid or anhydride in the presence of zinc chloride to yield a 9-substituted acridine.
+ batchelorc
+ 2014-03-12T09:00:00Z
+ doi:10.1039/b204243f
+ https://www.rsc.org/Merck-Index/reaction/r41/
+ Bernthsen reaction
+ RXNO
+ RXNO:0000519
+ Definition source Merck Index, modified for errors.
+ Bernthsen acridine synthesis
+
+
+
+
+ Reaction of a diarylamine in an organic acid or anhydride in the presence of zinc chloride to yield a 9-substituted acridine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Ring formation reaction where the intended product is a pyridine.
+ batchelorc
+ 2014-03-12T09:00:00Z
+ RXNO
+ RXNO:0000520
+ pyridine synthesis
+
+
+
+
+ Ring formation reaction where the intended product is a pyridine.
+ RSC:xp
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Ring formation reaction where the intended product is a carbazole.
+ batchelorc
+ 2014-03-12T09:00:00Z
+ RXNO
+ RXNO:0000521
+ carbazole synthesis
+
+
+
+
+ Ring formation reaction where the intended product is a carbazole.
+ RSC:xp
+
+
+
+
+
+
+
+
+ Reaction of a phenol, an aromatic aldehyde and a primary aromatic or heterocyclic amine to yield a Betti's base, also known as an alpha-aminobenzylphenol.
+ batchelorc
+ 2014-03-13T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r42/
+ Betti synthesis
+ RXNO
+ RXNO:0000522
+ Betti reaction
+
+
+
+
+ Reaction of a phenol, an aromatic aldehyde and a primary aromatic or heterocyclic amine to yield a Betti's base, also known as an alpha-aminobenzylphenol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of a terminal hydroxyketone or terminal halogenoketone with an aromatic amine to yield a 2-substituted indole.
+ batchelorc
+ 2014-03-13T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r45/
+ Bischler reaction
+ Bischler-Mohlau indole synthesis
+ Bischler-Mohlau reaction
+ Bischler-Möhlau reaction
+ RXNO
+ RXNO:0000523
+ Originally this involved a solvent but this need not be the case, see for example doi:10.1039/b719641e
+ Bischler-Möhlau indole synthesis
+
+
+
+
+ Reaction of a terminal hydroxyketone or terminal halogenoketone with an aromatic amine to yield a 2-substituted indole.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Cyclisation of an o-acylaminoacetophenone in alcoholic sodium hydroxide to form a substituted hydroxyquinoline.
+ batchelorc
+ 2014-03-24T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r70/
+ Camps cyclisation
+ Camps cyclization
+ RXNO
+ RXNO:0000524
+ The substituent on the amino nitrogen can affect the ratio of 1-hydroxy to 3-hydroxy products.
+ Camps quinoline synthesis
+
+
+
+
+ Cyclisation of an o-acylaminoacetophenone in alcoholic sodium hydroxide to form a substituted hydroxyquinoline.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Palladium-catalysed coupling of copper(I) acetylides with aryl halides to yield arylacetylenes.
+ batchelorc
+ 2014-03-25T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r73/
+ RXNO
+ RXNO:0000525
+ Castro-Stephens coupling
+
+
+
+
+ Palladium-catalysed coupling of copper(I) acetylides with aryl halides to yield arylacetylenes.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of carbonyl compounds with ammonia or an amine to yield a pyridine.
+ batchelorc
+ 2014-03-25T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r75/
+ RXNO
+ RXNO:0000526
+ Chichibabin pyridine synthesis
+
+
+
+
+ Reaction of carbonyl compounds with ammonia or an amine to yield a pyridine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ Reaction of an azacycle with an alkali-metal amide to yield an aminated azacycle.
+ batchelorc
+ 2014-03-25T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r76/
+ RXNO
+ RXNO:0000527
+ Chichibabin reaction
+
+
+
+
+ Reaction of an azacycle with an alkali-metal amide to yield an aminated azacycle.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of a carboxylic ester with a magnesium iodide alkylamide to yield a carboxamide.
+ batchelorc
+ 2014-03-27T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r52/
+ RXNO
+ RXNO:0000528
+ Bodroux reaction
+
+
+
+
+ Reaction of a carboxylic ester with a magnesium iodide alkylamide to yield a carboxamide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Condensation of beta-phenylethylmagnesium bromide with a cyclohexanone followed by cyclisation and dehydration in concentrated sulfuric acid to yield an octahydrophenanthrene.
+ batchelorc
+ 2014-03-27T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r53/
+ RXNO
+ RXNO:0000529
+ Bogert-Cook synthesis
+
+
+
+
+ Condensation of beta-phenylethylmagnesium bromide with a cyclohexanone followed by cyclisation and dehydration in concentrated sulfuric acid to yield an octahydrophenanthrene.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of a hydroxylated anthraquinone with fuming sulfuric acid or sulfuric acid in boric acid in the presence of a mercury or selenium catalyst to form a more hydroxylated anthraquinone.
+ batchelorc
+ 2014-03-27T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r54/
+ RXNO
+ RXNO:0000530
+ Bohn-Schmidt reaction
+
+
+
+
+ Reaction of a hydroxylated anthraquinone with fuming sulfuric acid or sulfuric acid in boric acid in the presence of a mercury or selenium catalyst to form a more hydroxylated anthraquinone.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Etherification of an aldehyde followed by bromination and reaction with a Grignard reagent followed by treatment with zinc to eliminate the halogen and alkoxy groups to produce an olefin.
+ batchelorc
+ 2014-03-27T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r55/
+ RXNO
+ RXNO:0000531
+ Boord olefin synthesis
+
+
+
+
+ Etherification of an aldehyde followed by bromination and reaction with a Grignard reagent followed by treatment with zinc to eliminate the halogen and alkoxy groups to produce an olefin.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Rearrangement of a cyclohexanone phenylhydrazone followed by oxidation to yield a carbazole.
+ batchelorc
+ 2014-03-27T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r56/
+ Borsche-Drechsel carbazole synthesis
+ Borsche-Drechsel cyclization
+ RXNO
+ RXNO:0000532
+ Borsche-Drechsel cyclisation
+
+
+
+
+ Rearrangement of a cyclohexanone phenylhydrazone followed by oxidation to yield a carbazole.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of an organomagnesium or organolithium compound with an N,N'-disubstituted formamide to yield the next homologous aldehyde.
+ batchelorc
+ 2014-03-27T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r57/
+ RXNO
+ RXNO:0000533
+ Bouveault aldehyde synthesis
+
+
+
+
+ Reaction of an organomagnesium or organolithium compound with an N,N'-disubstituted formamide to yield the next homologous aldehyde.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Diels-Alder reaction of a dienophile with a cationic aromatic azadiene to yield a bridged-ring system.
+ batchelorc
+ 2014-03-27T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r60/
+ Bradsher cyclization
+ Bradsher cycloaddition
+ RXNO
+ RXNO:0000534
+ Bradsher cyclisation
+
+
+
+
+ Diels-Alder reaction of a dienophile with a cationic aromatic azadiene to yield a bridged-ring system.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of an ortho-acyldiarylmethane, catalysed by acid, to yield an anthracene.
+ batchelorc
+ 2014-04-08T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r61/
+ RXNO
+ RXNO:0000535
+ Bradsher reaction
+
+
+
+
+ Reaction of an ortho-acyldiarylmethane, catalysed by acid, to yield an anthracene.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of a bromoarene that has an electrophilic group at the para-position with lithium bromide or lithium iodide followed by intramolecular cyclisation to yield a fused-ring system.
+ batchelorc
+ 2014-04-08T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r317/
+ RXNO
+ RXNO:0000536
+ Parham cyclisation
+
+
+
+
+ Reaction of a bromoarene that has an electrophilic group at the para-position with lithium bromide or lithium iodide followed by intramolecular cyclisation to yield a fused-ring system.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of an aliphatic aldehyde with a phenolic ether and hydrochloric acid to yield an alpha-chloroalkylphenolic ether.
+ batchelorc
+ 2014-04-14T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r357/
+ RXNO
+ RXNO:0000537
+ Quelet reaction
+
+
+
+
+ Reaction of an aliphatic aldehyde with a phenolic ether and hydrochloric acid to yield an alpha-chloroalkylphenolic ether.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Elimination of a water molecule from a secondary alcohol to yield an olefin.
+ batchelorc
+ 2014-04-14T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r77/
+ RXNO
+ RXNO:0000538
+ Chugaev reaction
+
+
+
+
+ Elimination of a water molecule from a secondary alcohol to yield an olefin.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Elimination of a hydroxylamine from an amine oxide by pyrolysis to yield an olefin.
+ batchelorc
+ 2014-04-14T09:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r85/
+ https://www.wikidata.org/wiki/Q900370
+ Cope reaction
+ RXNO
+ RXNO:0000539
+ Cope elimination
+
+
+
+
+ Elimination of a hydroxylamine from an amine oxide by pyrolysis to yield an olefin.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of an aniline with a nitrile in the presence of boron trichloride and a Lewis acid to yield an ortho-acylated aniline.
+ batchelorc
+ 2014-04-14T13:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r423/
+ RXNO
+ RXNO:0000540
+ Sugasawa reaction
+
+
+
+
+ Reaction of an aniline with a nitrile in the presence of boron trichloride and a Lewis acid to yield an ortho-acylated aniline.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A cross-coupling reaction between a Grignard reagent and an activated (aryl or vinyl) halide or triflate. The reaction is catalysed by a palladium catalyst.
+ batchelorc
+ 2014-04-14T13:00:00Z
+ RXNO
+ RXNO:0000541
+ palladium-catalysed Kumada coupling
+
+
+
+
+ A cross-coupling reaction between a Grignard reagent and an activated (aryl or vinyl) halide or triflate. The reaction is catalysed by a palladium catalyst.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A cross-coupling reaction between a Grignard reagent and an activated (aryl or vinyl) halide or triflate. The reaction is catalysed by a nickel catalyst.
+ batchelorc
+ 2014-04-14T13:00:00Z
+ RXNO
+ RXNO:0000542
+ nickel-catalysed Kumada coupling
+
+
+
+
+ A cross-coupling reaction between a Grignard reagent and an activated (aryl or vinyl) halide or triflate. The reaction is catalysed by a nickel catalyst.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+ https://orcid.org/0000-0002-4077-4719
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of a 1,2-diol with triethoxymethane under heat to yield an olefin.
+ batchelorc
+ 2014-04-15T11:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r121/
+ RXNO
+ RXNO:0000543
+ The reaction is stereospecific. It proceeds via a 1,3-dioxolane intermediate.
+ Eastwood reaction
+
+
+
+
+ Reaction of a 1,2-diol with triethoxymethane under heat to yield an olefin.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of silyl enol ethers with palladium acetate in acetonitrile to yield an alpha,beta-unsaturated ketone.
+ batchelorc
+ 2014-04-22T16:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r382/
+ RXNO
+ RXNO:0000544
+ Saegusa oxidation
+
+
+
+
+ Reaction of silyl enol ethers with palladium acetate in acetonitrile to yield an alpha,beta-unsaturated ketone.
+ doi:10.1021/jo00399a052
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of diphenylthiourea with lead carbonate and potassium cyanide to form a cyanoformidine followed by ring closure and acid hydrolysis to yield isatin.
+ batchelorc
+ 2014-04-24T15:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r384/
+ RXNO
+ RXNO:0000545
+ Sandmeyer diphenylurea isatin synthesis
+
+
+
+
+ Reaction of diphenylthiourea with lead carbonate and potassium cyanide to form a cyanoformidine followed by ring closure and acid hydrolysis to yield isatin.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of aniline, hydroxylamine and chloral hydrate to form an aniline intermediate followed by cyclization in acid and hydrolysis to yield isatin.
+ batchelorc
+ 2014-04-24T15:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r385/
+ RXNO
+ RXNO:0000546
+ Sandmeyer isonitrosoacetanilide isatin synthesis
+
+
+
+
+ Reaction of aniline, hydroxylamine and chloral hydrate to form an aniline intermediate followed by cyclization in acid and hydrolysis to yield isatin.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Oxidation of an alcohol with a pyridine-chromium trioxide complex to yield a carbonyl compound.
+ batchelorc
+ 2014-04-24T15:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r387/
+ RXNO
+ RXNO:0000547
+ Sarett oxidation
+
+
+
+
+ Oxidation of an alcohol with a pyridine-chromium trioxide complex to yield a carbonyl compound.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ Oxidation of a primary alcohol with a pyridine-chromium trioxide complex to yield an aldehyde.
+ batchelorc
+ 2014-04-24T15:00:00Z
+ https://www.wikidata.org/wiki/Q2227511
+ RXNO
+ RXNO:0000548
+ Sarett primary alcohol oxidation
+
+
+
+
+ Oxidation of a primary alcohol with a pyridine-chromium trioxide complex to yield an aldehyde.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ Oxidation of a secondary alcohol with a pyridine-chromium trioxide complex to yield a ketone.
+ batchelorc
+ 2014-04-24T15:00:00Z
+ RXNO
+ RXNO:0000549
+ Sarett secondary alcohol oxidation
+
+
+
+
+ Oxidation of a secondary alcohol with a pyridine-chromium trioxide complex to yield a ketone.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Oxidation of a primary alcohol with a pyridine-chromium trioxide complex in dichloromethane to yield an aldehyde.
+ batchelorc
+ 2014-04-24T15:00:00Z
+ https://www.rsc.org/Merck-Index/reaction/r387/
+ RXNO
+ RXNO:0000550
+ Collins oxidation
+
+
+
+
+ Oxidation of a primary alcohol with a pyridine-chromium trioxide complex in dichloromethane to yield an aldehyde.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ A functional group modification where a carbonyl oxygen is replaced by an imine.
+ RXNO
+ RXNO:0000551
+ reductive imination
+
+
+
+
+ A functional group modification where a carbonyl oxygen is replaced by an imine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reductive amination of an aldehyde with ammonium formate or formamide to form an amine.
+ RXNO
+ RXNO:0000552
+ Leuckart aldehyde reaction
+
+
+
+
+ Reductive amination of an aldehyde with ammonium formate or formamide to form an amine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reductive amination of a ketone with ammonium formate or formamide to form an amine.
+ RXNO
+ RXNO:0000553
+ Leuckart ketone reaction
+
+
+
+
+ Reductive amination of a ketone with ammonium formate or formamide to form an amine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Conversion of an alcohol to an alkyl bromide with triphenylphosphine and tetrabromomethane.
+ RXNO
+ RXNO:0000554
+ Appel bromination with tetrabromomethane
+
+
+
+
+ Conversion of an alcohol to an alkyl bromide with triphenylphosphine and tetrabromomethane.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Conversion of an alcohol to an alkyl bromide with triphenylphosphine and bromine.
+ RXNO
+ RXNO:0000555
+ Appel bromination with bromine
+
+
+
+
+ Conversion of an alcohol to an alkyl bromide with triphenylphosphine and bromine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of an aldehyde with tetrabromomethane and triphenylphosphine to yield a terminal dibromoolefin.
+ Corey-Fuchs reaction step 1
+ RXNO
+ RXNO:0000556
+ This is the first step of the Corey-Fuchs reaction. The second step is the Fritsch-Buttenberg-Wiechell rearrangement.
+ Corey-Fuchs terminal dibromoolefination
+
+
+
+
+ Reaction of an aldehyde with tetrabromomethane and triphenylphosphine to yield a terminal dibromoolefin.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000557
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000624 for Heck-type reaction and RXNO:0000603 for cross-coupling.
+ obsolete: Heck-type reaction/cross-coupling
+ true
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000558
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000625 for the bromo Heck reaction and RXNO:0000604 for Liebeskind-Srogl coupling.
+ obsolete: bromo Heck reaction/Liebeskind-Srogl coupling
+ true
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000559
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000626 for the chloro Heck reaction and RXNO:0000605 for Fukuyama coupling.
+ obsolete: chloro Heck reaction/Fukuyama coupling
+ true
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000560
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000627 for the iodo Heck reaction and RXNO:0000606 for the chloride Finkelstein reaction.
+ obsolete: iodo Heck reaction/chloride Finkelstein reaction
+ true
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000561
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000628 for the triflyloxy Heck reaction and RXNO:0000607 for the bromide Finkelstein reaction.
+ obsolete: triflyloxy Heck reaction/bromide Finkelstein reaction
+ true
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000562
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000629 for the bromo Heck-type reaction and RXNO:0000608 for the sulfonate ester Finkelstein reaction.
+ obsolete: bromo Heck-type reaction/sulfonate ester Finkelstein reaction
+ true
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000563
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000630 for the chloro Heck-type reaction and RXNO:0000609 for Sandmeyer fluorination.
+ obsolete: chloro Heck-type reaction/Sandmeyer fluorination
+ true
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000564
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000631 for acyclic Beckmann rearrangement and RXNO:0000610 for Sandmeyer chlorination.
+ obsolete: acyclic Beckmann rearrangement/Sandmeyer chlorination
+ true
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000565
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000632 for Baeyer-Emmerling indole synthesis and RXNO:0000611 for Sandmeyer bromination.
+ obsolete: Baeyer–Emmerling indole synthesis/Sandmeyer bromination
+ true
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000566
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000633 for bromo Sonogashira coupling and RXNO:0000612 for Sandmeyer iodination.
+ obsolete: bromo Sonogashira coupling/Sandmeyer iodination
+ true
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000567
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000634 for bromo Suzuki coupling and RXNO:0000613 for the iodo Heck reaction.
+ obsolete: bromo Suzuki coupling/iodo Heck reaction
+ true
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000568
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000635 for bromo Suzuki-type coupling and RXNO:0000628 for the triflyloxy Heck reaction.
+ obsolete: bromo Suzuki-type coupling/triflyloxy Heck reaction
+ true
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000569
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000636 for bromolactonization and RXNO:0000629 for the bromo Heck-type reaction.
+ obsolete: bromolactonization/bromo Heck-type reaction
+ true
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000570
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000637 for chloro Sonogashira coupling and RXNO:0000630 for the chloro Heck-type reaction.
+ obsolete: chloro Sonogashira coupling/chloro Heck-type reaction
+ true
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000571
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000638 for chloro Suzuki coupling and RXNO:0000624 for the Heck-type reaction.
+ obsolete: chloro Suzuki coupling/Heck-type reaction
+ true
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000572
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000639 for chloro Suzuki-type coupling and RXNO:0000625 for the bromo Heck reaction.
+ obsolete: chloro Suzuki-type coupling/bromo Heck reaction
+ true
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000573
+ This term has been obsoleted because the ID was inadvertently reused for two classes. See RXNO:0000640 for chlorolactonization and RXNO:0000626 for the chloro Heck reaction.
+ obsolete: chlorolactonization/chloro Heck reaction
+ true
+
+
+
+
+
+
+
+
+
+ A Beckmann rearrangement which produces a cyclic product.
+ NAMERXN:4.1.6
+ RXNO
+ RXNO:0000574
+ cyclic Beckmann rearrangement
+
+
+
+
+ A Beckmann rearrangement which produces a cyclic product.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Dess-Martin oxidation of a primary alcohol to an aldehyde.
+ NAMERXN:8.1.2
+ aldehyde Dess-Martin oxidation
+ RXNO
+ RXNO:0000575
+ Dess-Martin aldehyde oxidation
+
+
+
+
+ A Dess-Martin oxidation of a primary alcohol to an aldehyde.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Dess-Martin oxidation of a secondary alcohol to a ketone.
+ NAMERXN:8.1.3
+ ketone Dess-Martin oxidation
+ RXNO
+ RXNO:0000576
+ Dess-Martin ketone oxidation
+
+
+
+
+ A Dess-Martin oxidation of a secondary alcohol to a ketone.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Synthesis of a quinoline by reaction of a 2-aminobenzaldehyde with a ketone.
+ NAMERXN:4.1.29
+ https://www.wikidata.org/wiki/Q1058388
+ Friedlaender synthesis
+ Friedlander synthesis
+ Friedländer synthesis
+ RXNO
+ RXNO:0000577
+ Friedlander quinoline synthesis
+
+
+
+
+ Synthesis of a quinoline by reaction of a 2-aminobenzaldehyde with a ketone.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of an aldehyde or ketone with an alpha-cyanoester to form a 2-aminothiophene.
+ NAMERXN:4.3.4
+ https://www.wikidata.org/wiki/Q240091
+ Gewald thiophene synthesis
+ RXNO
+ RXNO:0000578
+ Gewald reaction
+
+
+
+
+ Reaction of an aldehyde or ketone with an alpha-cyanoester to form a 2-aminothiophene.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Sonogashira coupling where the aryl halide is an aryl iodide.
+ NAMERXN:3.3.4
+ RXNO
+ RXNO:0000579
+ iodo Sonogashira coupling
+
+
+
+
+ A Sonogashira coupling where the aryl halide is an aryl iodide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ A Suzuki coupling where the halide is an iodide.
+ NAMERXN:3.1.3
+ iodo Suzuki-Miyaura coupling
+ RXNO
+ RXNO:0000580
+ iodo Suzuki coupling
+
+
+
+
+ A Suzuki coupling where the halide is an iodide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Suzuki-type coupling where the halide is an iodide.
+ NAMERXN:3.1.7
+ iodo Suzuki-Miyaura-type coupling
+ RXNO
+ RXNO:0000581
+ iodo Suzuki-type coupling
+
+
+
+
+ A Suzuki-type coupling where the halide is an iodide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A halolactionization where the halide is an iodide.
+ NAMERXN:4.2.15
+ https://www.wikidata.org/wiki/Q6062283
+ iodolactonisation
+ RXNO
+ RXNO:0000582
+ iodolactonization
+
+
+
+
+ A halolactionization where the halide is an iodide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An azacycle synthesis where the product is a 4-oxo-3,4-dihydroquinazoline and the reactants are a 2-aminobenzoic acid and an amide.
+ NAMERXN:4.1.30
+ https://www.wikidata.org/wiki/Q1059542
+ RXNO
+ RXNO:0000583
+ Niementowski quinazoline synthesis
+
+
+
+
+ An azacycle synthesis where the product is a 4-oxo-3,4-dihydroquinazoline and the reactants are a 2-aminobenzoic acid and an amide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A quinoline synthesis where the product is a gamma-hydroxyquinoline and the reactants are a 2-aminobenzoic acid and an aldehyde or ketone.
+ NAMERXN:4.1.31
+ https://www.wikidata.org/wiki/Q2733837
+ RXNO
+ RXNO:0000584
+ Niementowski quinoline synthesis
+
+
+
+
+ A quinoline synthesis where the product is a gamma-hydroxyquinoline and the reactants are a 2-aminobenzoic acid and an aldehyde or ketone.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An azacycle synthesis where the product is an isoquinoline and the reactants are a benzaldehyde and a 2,2-dialkoxyethylamine.
+ NAMERXN:4.1.65
+ https://www.wikidata.org/wiki/Q18217151
+ Pomeranz–Fritsch cyclization
+ Pomeranz–Fritsch isoquinoline synthesis
+ RXNO
+ RXNO:0000585
+ Pomeranz–Fritsch reaction
+
+
+
+
+ An azacycle synthesis where the product is an isoquinoline and the reactants are a benzaldehyde and a 2,2-dialkoxyethylamine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An O-acylation to ester where dicyclohexylcarbodiimide is used as a coupling reagent and 4-dimethylaminopyridine as a catalyst.
+ NAMERXN:2.6.9
+ https://www.wikidata.org/wiki/Q695687
+ RXNO
+ RXNO:0000586
+ Steglich esterification
+
+
+
+
+ An O-acylation to ester where dicyclohexylcarbodiimide is used as a coupling reagent and 4-dimethylaminopyridine as a catalyst.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Sonogashira coupling where the role of the halide is played by a triflyloxy group.
+ NAMERXN:3.3.5
+ Triflyloxy Sonogashira coupling
+ RXNO
+ RXNO:0000587
+ triflyloxy Sonogashira coupling
+
+
+
+
+ A Sonogashira coupling where the role of the halide is played by a triflyloxy group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ A Suzuki coupling where the rule of the halide is played by a triflyloxy group.
+ NAMERXN:3.1.4
+ Triflyloxy Suzuki coupling
+ triflyloxy Suzuki-Miyaura coupling
+ RXNO
+ RXNO:0000588
+ triflyloxy Suzuki coupling
+
+
+
+
+ A Suzuki coupling where the rule of the halide is played by a triflyloxy group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Suzuki-type coupling where the rule of the halide is played by a triflyloxy group.
+ NAMERXN:3.1.8
+ Triflyloxy Suzuki-type coupling
+ triflyloxy Suzuki-Miyaura-type coupling
+ RXNO
+ RXNO:0000589
+ triflyloxy Suzuki-type coupling
+
+
+
+
+ A Suzuki-type coupling where the rule of the halide is played by a triflyloxy group.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ Synthesis of an aziridine by dehydrating a beta aminoalcohol with sulfuric acid.
+ NAMERXN:4.1.66
+ https://doi.org/10.1021/ja01314a504
+ https://www.wikidata.org/wiki/Q900233
+ Wenker aziridine synthesis
+ RXNO
+ RXNO:0000590
+ Wenker synthesis
+
+
+
+
+ Synthesis of an aziridine by dehydrating a beta aminoalcohol with sulfuric acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of an alpha-diketone with a dialkyl thiodiacetate to form a thiophene dicarboxylic acid.
+ https://www.rsc.org/Merck-Index/reaction/r202/
+ https://www.wikidata.org/wiki/Q18020904
+ RXNO
+ RXNO:0000591
+ Hinsberg thiophene synthesis
+
+
+
+
+ Reaction of an alpha-diketone with a dialkyl thiodiacetate to form a thiophene dicarboxylic acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ The coupling of a boronic acid or boronic ester with an unsaturated halide, triflate or sulfonate.
+ RXNO
+ RXNO:0000592
+ Suzuki-type coupling
+
+
+
+
+ The coupling of a boronic acid or boronic ester with an unsaturated halide, triflate or sulfonate.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Addition of a carboxylic acid oxygen and halogen across a carbon-carbon double bond to form a lactone.
+ halolactonisation
+ RXNO
+ RXNO:0000593
+ halolactonization
+
+
+
+
+ Addition of a carboxylic acid oxygen and halogen across a carbon-carbon double bond to form a lactone.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Expansion of a pyrrole ring by heating with a halogeno compond to form a 3-halogenopyridine.
+ https://www.rsc.org/Merck-Index/reaction/r78/
+ https://www.wikidata.org/wiki/Q6151790
+ RXNO
+ RXNO:0000594
+ Ciamician-Dennstedt rearrangement
+
+
+
+
+ Expansion of a pyrrole ring by heating with a halogeno compond to form a 3-halogenopyridine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Condensation of an aromatic aldehyde with an aliphatic aldehyde or ketone in the presence of a relatively strong base to from an alpha,beta-unsaturated aldehyde or ketone.
+ https://www.rsc.org/Merck-Index/reaction/r81/
+ https://www.wikidata.org/wiki/Q56298266
+ RXNO
+ RXNO:0000595
+ Claisen-Schmidt condensation
+
+
+
+
+ Condensation of an aromatic aldehyde with an aliphatic aldehyde or ketone in the presence of a relatively strong base to from an alpha,beta-unsaturated aldehyde or ketone.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+ RXNO
+ RXNO:0000596
+ this ID has been obsoleted because it was used for two different classes.
+ obsolete: Combes quinoline synthesis/Conrad%E2%80%93Limpach_synthesis
+ true
+
+
+
+
+
+
+
+
+
+ Enantioselective reduction of a ketone to an alcohol with a chiral oxazaborolidine.
+ https://www.rsc.org/Merck-Index/reaction/r87/
+ https://www.wikidata.org/wiki/Q903598
+ CBS reduction
+ Corey-Itsuno reduction
+ RXNO
+ RXNO:0000597
+ Corey-Bakshi-Shibata reduction
+
+
+
+
+ Enantioselective reduction of a ketone to an alcohol with a chiral oxazaborolidine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reaction of a sulfur ylide with a double-bond to produce a three-membered ring.
+ https://www.rsc.org/Merck-Index/reaction/r88/
+ https://www.wikidata.org/wiki/Q1582682
+ Corey-Chaykovsky reaction
+ RXNO
+ RXNO:0000598
+ Johnson-Corey-Chaykovsky reaction
+
+
+
+
+ Reaction of a sulfur ylide with a double-bond to produce a three-membered ring.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of a sulfur ylide with a ketone to produce an epoxide.
+ RXNO
+ RXNO:0000599
+ Johnson-Corey-Chaykovsky epoxide synthesis
+
+
+
+
+ Reaction of a sulfur ylide with a ketone to produce an epoxide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of a sulfur ylide with an olefin to produce a cyclopropane.
+ RXNO
+ RXNO:0000600
+ Johnson-Corey-Chaykovsky cyclopropane synthesis
+
+
+
+
+ Reaction of a sulfur ylide with an olefin to produce a cyclopropane.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of a sulfur ylide with an imine to produce an aziridine.
+ RXNO
+ RXNO:0000601
+ Johnson-Corey-Chaykovsky aziridine synthesis
+
+
+
+
+ Reaction of a sulfur ylide with an imine to produce an aziridine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of a sulfur ylide with a thione to produce a thiirane.
+ RXNO
+ RXNO:0000602
+ Johnson-Corey-Chaykovsky thiirane synthesis
+
+
+
+
+ Reaction of a sulfur ylide with a thione to produce a thiirane.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A joining reaction where a carbon-carbon bond is formed between unlike moieties.
+ https://www.wikidata.org/wiki/Q7127709
+ RXNO
+ RXNO:0000603
+ cross-coupling
+
+
+
+
+ A joining reaction where a carbon-carbon bond is formed between unlike moieties.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A cross-coupling reaction where a thioester and a boronic acid react to form a ketone. It uses a metal catalyst.
+ https://www.wikidata.org/wiki/Q6543886
+ RXNO
+ RXNO:0000604
+ Liebeskind-Srogl coupling
+
+
+
+
+ A cross-coupling reaction where a thioester and a boronic acid react to form a ketone. It uses a metal catalyst.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A cross-coupling reaction where a thioester and an organozinc halide react to form a ketone. It uses a palladium catalyst.
+ https://www.wikidata.org/wiki/Q5507762
+ RXNO
+ RXNO:0000605
+ Fukuyama coupling
+
+
+
+
+ A cross-coupling reaction where a thioester and an organozinc halide react to form a ketone. It uses a palladium catalyst.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ The conversion of an alkyl chloride to an alkyl iodide by SN2 substitution.The reaction relies upon the equilibrium being pushed to completion by precipitation.
+ RXNO
+ RXNO:0000606
+ chloride Finkelstein reaction
+
+
+
+
+ The conversion of an alkyl chloride to an alkyl iodide by SN2 substitution.The reaction relies upon the equilibrium being pushed to completion by precipitation.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ The conversion of an alkyl bromide to an alkyl iodide by SN2 substitution.The reaction relies upon the equilibrium being pushed to completion by precipitation.
+ RXNO
+ RXNO:0000607
+ bromide Finkelstein reaction
+
+
+
+
+ The conversion of an alkyl bromide to an alkyl iodide by SN2 substitution.The reaction relies upon the equilibrium being pushed to completion by precipitation.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ The conversion of an alkyl sulfonate ester to an alkyl iodide by SN2 substitution.The reaction relies upon the equilibrium being pushed to completion by precipitation.
+ RXNO
+ RXNO:0000608
+ sulfonate ester Finkelstein reaction
+
+
+
+
+ The conversion of an alkyl sulfonate ester to an alkyl iodide by SN2 substitution.The reaction relies upon the equilibrium being pushed to completion by precipitation.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with a copper(I) fluoride to form an aromatic fluoride.
+ RXNO
+ RXNO:0000609
+ Sandmeyer fluorination
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with a copper(I) fluoride to form an aromatic fluoride.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with a copper(I) chloride to form an aromatic chloride.
+ RXNO
+ RXNO:0000610
+ Sandmeyer chlorination
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with a copper(I) chloride to form an aromatic chloride.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with a copper(I) bromide to form an aromatic bromide.
+ RXNO
+ RXNO:0000611
+ Sandmeyer bromination
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with a copper(I) bromide to form an aromatic bromide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with a copper(I) iodide to form an aromatic iodide.
+ RXNO
+ RXNO:0000612
+ Sandmeyer iodination
+
+
+
+
+ An aromatic substitution reaction where an aryl diazonium salt reacts with a copper(I) iodide to form an aromatic iodide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A planned reaction in which one of the products contains an imidazole system that was not in any of the reactants.
+ RXNO
+ RXNO:0000613
+ imidazole synthesis
+
+
+
+
+ A planned reaction in which one of the products contains an imidazole system that was not in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A planned reaction in which one of the products contains an indazole system that was not in any of the reactants.
+ RXNO
+ RXNO:0000614
+ indazole synthesis
+
+
+
+
+ A planned reaction in which one of the products contains an indazole system that was not in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A planned reaction in which one of the products contains a piperazine system that was not in any of the reactants.
+ RXNO
+ RXNO:0000615
+ piperazine synthesis
+
+
+
+
+ A planned reaction in which one of the products contains a piperazine system that was not in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A planned reaction in which one of the products contains a piperidine system that was not in any of the reactants.
+ RXNO
+ RXNO:0000616
+ piperidine synthesis
+
+
+
+
+ A planned reaction in which one of the products contains a piperidine system that was not in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A planned reaction in which one of the products contains a pyrrolidine system that was not in any of the reactants.
+ RXNO
+ RXNO:0000617
+ pyrrolidine synthesis
+
+
+
+
+ A planned reaction in which one of the products contains a pyrrolidine system that was not in any of the reactants.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An azacycle synthesis in which pyrrolidines or piperidines are formed by decomposition of protonated N-haloamines.
+ https://www.rsc.org/Merck-Index/reaction/r207/
+ https://www.wikidata.org/wiki/Q5876831
+ Hofmann-Löffler reaction
+ RXNO
+ RXNO:0000618
+ Hofmann-Löffler-Freytag reaction
+
+
+
+
+ An azacycle synthesis in which pyrrolidines or piperidines are formed by decomposition of protonated N-haloamines.
+ https://www.rsc.org/Merck-Index/reaction/r207/hofmann-löffler-freytag%20reaction
+
+
+
+
+
+
+
+
+ A Hofmann-Löffler-Freytag reaction in which the product is a piperidine.
+ RXNO
+ RXNO:0000619
+ Hofmann-Löffler-Freytag piperidine synthesis
+
+
+
+
+ A Hofmann-Löffler-Freytag reaction in which the product is a piperidine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Hofmann-Löffler-Freytag reaction in which the product is a pyrrolidine.
+ RXNO
+ RXNO:0000620
+ Hofmann-Löffler-Freytag pyrrolidine synthesis
+
+
+
+
+ A Hofmann-Löffler-Freytag reaction in which the product is a pyrrolidine.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ An alpha-halogenation reaction where a carboxylic acid reacts with dibromine to form an alpha-bromocarboxylic acid.
+ https://www.rsc.org/Merck-Index/reaction/r194
+ https://www.wikidata.org/wiki/Q902219
+ Hell-Volhard-Zelinsky halogenation
+ RXNO
+ RXNO:0000621
+ Hell-Volhard-Zelinsky reaction
+
+
+
+
+ An alpha-halogenation reaction where a carboxylic acid reacts with dibromine to form an alpha-bromocarboxylic acid.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Meerwein-Ponndorf-Verley reduction of an aldehyde to the corresponding primary alcohol.
+ RXNO
+ RXNO:0000622
+ Meerwein-Ponndorf-Verley reduction of an aldehyde
+
+
+
+
+ Meerwein-Ponndorf-Verley reduction of an aldehyde to the corresponding primary alcohol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Meerwein-Ponndorf-Verley reduction of a ketone to the corresponding secondary alcohol.
+ RXNO
+ RXNO:0000623
+ Meerwein-Ponndorf-Verley reduction of a ketone
+
+
+
+
+ Meerwein-Ponndorf-Verley reduction of a ketone to the corresponding secondary alcohol.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction where an organohalide or triflate couples to a terminal olefin to produce an internal olefin.
+ RXNO
+ RXNO:0000624
+ Heck-type reaction
+
+
+
+
+ A carbon-carbon coupling reaction where an organohalide or triflate couples to a terminal olefin to produce an internal olefin.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+ A Heck reaction where an organobromide couples to a terminal olefin to produce an internal olefin, catalysed by palladium.
+ RXNO
+ RXNO:0000625
+ obsolete: bromo Heck reaction
+ true
+
+
+
+
+ A Heck reaction where an organobromide couples to a terminal olefin to produce an internal olefin, catalysed by palladium.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ A Heck reaction where an organochloride couples to a terminal olefin to produce an internal olefin, catalysed by palladium.
+ RXNO
+ RXNO:0000626
+ chloro Heck reaction
+
+
+
+
+ A Heck reaction where an organochloride couples to a terminal olefin to produce an internal olefin, catalysed by palladium.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Heck reaction where an organoiodide couples to a terminal olefin to produce an internal olefin, catalysed by palladium.
+ RXNO
+ RXNO:0000627
+ iodo Heck reaction
+
+
+
+
+ A Heck reaction where an organoiodide couples to a terminal olefin to produce an internal olefin, catalysed by palladium.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Heck reaction where an organotriflate couples to a terminal olefin to produce an internal olefin, catalysed by palladium.
+ RXNO
+ RXNO:0000628
+ triflyloxy Heck reaction
+
+
+
+
+ A Heck reaction where an organotriflate couples to a terminal olefin to produce an internal olefin, catalysed by palladium.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Heck-type reaction where an organobromide couples to a terminal olefin to produce an internal olefin.
+ RXNO
+ RXNO:0000629
+ bromo Heck-type reaction
+
+
+
+
+ A Heck-type reaction where an organobromide couples to a terminal olefin to produce an internal olefin.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Heck-type reaction where an organochloride couples to a terminal olefin to produce an internal olefin.
+ RXNO
+ RXNO:0000630
+ chloro Heck-type reaction
+
+
+
+
+ A Heck-type reaction where an organochloride couples to a terminal olefin to produce an internal olefin.
+ RSC:db
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Beckmann rearrangement where an acyclic amide is formed.
+ NAMERXN:2.8.1
+ RXNO
+ RXNO:0000631
+ acyclic Beckmann rearrangement
+
+
+
+
+ A Beckmann rearrangement where an acyclic amide is formed.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ An indole synthesis where an ortho-nitrocinnamic acid reacts with iron powder in a basic solution to form an indole.
+ NAMERXN:4.1.41
+ https://doi.org/10.1002/cber.186900201268
+ https://www.wikidata.org/wiki/Q3159940
+ RXNO
+ RXNO:0000632
+ Baeyer–Emmerling indole synthesis
+
+
+
+
+ An indole synthesis where an ortho-nitrocinnamic acid reacts with iron powder in a basic solution to form an indole.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Sonogashira coupling where the aryl halide is an aryl bromide.
+ NAMERXN:3.3.2
+ Bromo Sonogashira coupling
+ RXNO
+ RXNO:0000633
+ bromo Sonogashira coupling
+
+
+
+
+ A Sonogashira coupling where the aryl halide is an aryl bromide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ A Suzuki coupling where the halide is a bromide.
+ NAMERXN:3.1.1
+ Bromo Suzuki coupling
+ bromo Suzuki-Miyaura coupling
+ RXNO
+ RXNO:0000634
+ bromo Suzuki coupling
+
+
+
+
+ A Suzuki coupling where the halide is a bromide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Suzuki-type coupling where the halide is a bromide.
+ NAMERXN:3.1.5
+ Bromo Suzuki-type coupling
+ bromo Suzuki-Miyaura-type coupling
+ RXNO
+ RXNO:0000635
+ bromo Suzuki-type coupling
+
+
+
+
+ A Suzuki-type coupling where the halide is a bromide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A halolactionization where the halide is a bromide.
+ NAMERXN:4.2.13
+ bromolactonisation
+ RXNO
+ RXNO:0000636
+ bromolactonization
+
+
+
+
+ A halolactionization where the halide is a bromide.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Sonogashira coupling where the aryl halide is an aryl chloride.
+ NAMERXN:3.3.3
+ Chloro Sonogashira coupling
+ RXNO
+ RXNO:0000637
+ chloro Sonogashira coupling
+
+
+
+
+ A Sonogashira coupling where the aryl halide is an aryl chloride.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ A Suzuki coupling where the halide is a chloride.
+ NAMERXN:3.1.2
+ Chloro Suzuki coupling
+ chloro Suzuki-Miyaura coupling
+ RXNO
+ RXNO:0000638
+ chloro Suzuki coupling
+
+
+
+
+ A Suzuki coupling where the halide is a chloride.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A Suzuki-type coupling where the halide is a chloride.
+ NAMERXN:3.1.6
+ Chloro Suzuki-type coupling
+ chloro Suzuki-Miyaura-type coupling
+ RXNO
+ RXNO:0000639
+ chloro Suzuki-type coupling
+
+
+
+
+ A Suzuki-type coupling where the halide is a chloride.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A halolactionization where the halide is a chloride.
+ NAMERXN:4.2.14
+ chlorolactonisation
+ RXNO
+ RXNO:0000640
+ chlorolactonization
+
+
+
+
+ A halolactionization where the halide is a chloride.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ Reaction of an arylamine wtih a beta-ketoester to yield a 4-hydroxyquinoline.
+ https://en.wikipedia.org/wiki/Conrad%E2%80%93Limpach_synthesis
+ https://www.rsc.org/Merck-Index/reaction/r84/
+ https://www.wikidata.org/wiki/Q1944895
+ Conrad-Limpach cyclization
+ Conrad-Limpach synthesis
+ RXNO
+ RXNO:0000641
+ Conrad-Limpach cyclisation
+
+
+
+
+ Reaction of an arylamine wtih a beta-ketoester to yield a 4-hydroxyquinoline.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ Reaction of a beta-diketone with a primary arylamine to yield a quinoline. It is acid-catalysed.
+ https://en.wikipedia.org/wiki/Combes_quinoline_synthesis
+ https://www.rsc.org/Merck-Index/reaction/r83/
+ https://www.wikidata.org/wiki/Q1058068
+ RXNO
+ RXNO:0000642
+ Combes quinoline synthesis
+
+
+
+
+ Reaction of a beta-diketone with a primary arylamine to yield a quinoline. It is acid-catalysed.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A 1,3-dipolar cycloaddition reaction where a fullerene reacts with an aldehyde and an amino acid to form a pyrrolidinofullerene.
+ https://www.wikidata.org/wiki/Q4391481
+ RXNO
+ RXNO:0000643
+ Prato reaction
+
+
+
+
+ A 1,3-dipolar cycloaddition reaction where a fullerene reacts with an aldehyde and an amino acid to form a pyrrolidinofullerene.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A rearrangement of a 2-furylcarbinol to a 4-hydroxycyclopentenone. It is acid-catalysed.
+ https://www.wikidata.org/wiki/Q3319193
+ RXNO
+ RXNO:0000644
+ Piancatelli rearrangement
+
+
+
+
+ A rearrangement of a 2-furylcarbinol to a 4-hydroxycyclopentenone. It is acid-catalysed.
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A ring-breaking reaction where a pyrrolidinofullerene yields a fullerene. The substituted fullerene is heated with a dipolarophile and a catalyst.
+ RXNO
+ RXNO:0000645
+ retro-Prato reaction
+
+
+
+
+ A ring-breaking reaction where a pyrrolidinofullerene yields a fullerene. The substituted fullerene is heated with a dipolarophile and a catalyst.
+ https://doi.org/10.1002/anie.200502556
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A cycloaddition where a fullerene reacts with diethyl bromomalonate to form a methanofullerene.
+ https://www.wikidata.org/wiki/Q1054818
+ RXNO
+ RXNO:0000646
+ Bingel reaction
+
+
+
+
+ A cycloaddition where a fullerene reacts with diethyl bromomalonate to form a methanofullerene.
+ https://doi.org/10.1002/cber.19931260829
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A cyclisation where a hydroxyl group acts as the nucleophile in a Wacker-Tsuji oxidation accompanied by beta-hydride elimination, forming a ring.
+ Wacker cyclization
+ RXNO
+ RXNO:0000647
+ Wacker cyclisation
+
+
+
+
+ A cyclisation where a hydroxyl group acts as the nucleophile in a Wacker-Tsuji oxidation accompanied by beta-hydride elimination, forming a ring.
+ http://organicreactions.org/index.php/Wacker_oxidation
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ A cyclisation where an amino group acts as the nucleophile in a Wacker-Tsuji oxidation accompanied by beta-hydride elimination, forming a ring.
+ aza-Wacker cyclization
+ RXNO
+ RXNO:0000648
+ aza-Wacker cyclisation
+
+
+
+
+ A cyclisation where an amino group acts as the nucleophile in a Wacker-Tsuji oxidation accompanied by beta-hydride elimination, forming a ring.
+ http://organicreactions.org/index.php/Wacker_oxidation
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A cleaving reaction where an olefin is dihydroxylated with osmium tetroxide and undergoes a Malaprade reaction to yield two aldehydes, two ketones, or an aldehyde and a ketone.
+ https://www.wikidata.org/wiki/Q6521154
+ RXNO
+ RXNO:0000649
+ Lemieux-Johnson oxidation
+
+
+
+
+ A cleaving reaction where an olefin is dihydroxylated with osmium tetroxide and undergoes a Malaprade reaction to yield two aldehydes, two ketones, or an aldehyde and a ketone.
+ https://doi.org/10.1021/jo01110a606
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+
+ A cleaving reaction of a 1,2-diol using periodic acid to give the corresponding carbonyl compounds.
+ https://www.wikidata.org/wiki/Q10851620
+ RXNO
+ RXNO:0000650
+ Malaprade reaction
+
+
+
+
+ A cleaving reaction of a 1,2-diol using periodic acid to give the corresponding carbonyl compounds.
+ https://doi.org/10.1039/C8CC09208G
+ https://orcid.org/0000-0001-5985-7429
+
+
+
+
+
+
+
+
+ The oxidation of a 1,2-glycol with Fenton's reagent (hydrogen peroxide and iron salts) to give an alpha-hydroxy aldehyde.
+ RXNO
+ RXNO:0000651
+ Fenton 1,2-glycol oxidation
+
+
+
+
+ The oxidation of a 1,2-glycol with Fenton's reagent (hydrogen peroxide and iron salts) to give an alpha-hydroxy aldehyde.
+ rsc:db
+
+
+
+
+
+
+
+
+ The oxidation of an alpha-hydroxy carboxylic acid with Fenton's reagent to give an alpha-keto carboxylic acid.
+ RXNO
+ RXNO:0000652
+ Fenton alpha-hydroxy carboxylic acid oxidation
+
+
+
+
+ The oxidation of an alpha-hydroxy carboxylic acid with Fenton's reagent to give an alpha-keto carboxylic acid.
+ RSC:db
+
+
+
+
+
+
+
+
+ The reaction of the components of Fenton's reagent, viz. reduction of hydrogen peroxide by Fe(II) , producing an hydroxyl radical.
+ RXNO
+ RXNO:0000653
+ Fenton hydrogen peroxide reduction
+
+
+
+
+ The reaction of the components of Fenton's reagent, viz. reduction of hydrogen peroxide by Fe(II) , producing an hydroxyl radical.
+ RSC:db
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The Mukaiyama hydration is an organic reaction involving formal addition of an equivalent of water across an alkene by the action of catalytic bis(acetylacetonato)cobalt(II) complex, phenylsilane and atmospheric oxygen.
+
+ 2021-05-11T07:40:36Z
+ RXNO
+ RXNO:0000654
+ Mukaiyama hydration
+
+
+
+
+ The Mukaiyama hydration is an organic reaction involving formal addition of an equivalent of water across an alkene by the action of catalytic bis(acetylacetonato)cobalt(II) complex, phenylsilane and atmospheric oxygen.
+ https://en.wikipedia.org/wiki/Mukaiyama_hydration
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A reaction between an alkyne and a carbonyl group under basic conditions in which a terminal alkyne serves as the CH-acidic moiety. When the carbonyl is an aldehyde, the 'Favorskii rearrangement' (RXNO:0000385) takes place and leads to an enone.
+
+ 2021-05-17T08:17:36Z
+ RXNO
+ Faworski-Babayan reaction
+ RXNO:0000655
+ Favorskii reaction
+
+
+
+
+ A reaction between an alkyne and a carbonyl group under basic conditions in which a terminal alkyne serves as the CH-acidic moiety. When the carbonyl is an aldehyde, the 'Favorskii rearrangement' (RXNO:0000385) takes place and leads to an enone.
+ https://en.wikipedia.org/wiki/Favorskii_reaction
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Reductions with diimide are a chemical reactions that convert unsaturated organic compounds to reduced alkane products. In the process, diimide is oxidized to dinitrogen.
+
+ 2021-05-17T08:35:08Z
+ RXNO
+ RXNO:0000656
+ Diimide reduction
+
+
+
+
+ Reductions with diimide are a chemical reactions that convert unsaturated organic compounds to reduced alkane products. In the process, diimide is oxidized to dinitrogen.
+ https://en.wikipedia.org/wiki/Reductions_with_diimide
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A protection reaction where the reactive centre is a carbonyl oxygen.
+
+ 2021-05-17T09:33:23Z
+ RXNO
+ RXNO:0000657
+ carbonyl group protection
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The acid-catalyzed formation of an acetal (or ketal) to protect a carbonyl group by nucleophilic addition of an alcohol to an aldehyde (or ketone) with the elimination of water.
+
+ 2021-05-17T09:38:59Z
+ RXNO
+ acetalisation
+ acetalization
+ RXNO:0000658
+ acetal protection
+
+
+
+
+ The acid-catalyzed formation of an acetal (or ketal) to protect a carbonyl group by nucleophilic addition of an alcohol to an aldehyde (or ketone) with the elimination of water.
+ https://en.wikipedia.org/wiki/Acetal
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A chemical reaction that allows the generation of boronates from vinyl or aryl halides with the cross-coupling of bis(pinacolato)diboron under basic conditions.
+
+ 2021-11-04T10:48:44Z
+ Miyaura boration
+ Miyaura borylation reaction
+ RXNO
+ RXNO:0000659
+ Miyaura borylation
+
+
+
+
+ A chemical reaction that allows the generation of boronates from vinyl or aryl halides with the cross-coupling of bis(pinacolato)diboron under basic conditions.
+ https://www.organic-chemistry.org/namedreactions/miyaura-borylation-reaction.shtm
+ https://www.rsc.org/Merck-Index/reaction/r288/miyaura%20boration?q=unauthorize
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A chemical reaction for the stereoselective synthesis of an olefin from a 1,2-diol.
+
+ 2021-11-04T11:03:16Z
+ RXNO
+ Corey-Winter fragmentation
+ Corey-Winter olefination
+ Corey–Winter olefin synthesis
+ RXNO:0000660
+ Corey-Winter elimination
+
+
+
+
+ A chemical reaction for the stereoselective synthesis of an olefin from a 1,2-diol.
+ https://en.wikipedia.org/wiki/Corey%E2%80%93Winter_olefin_synthesis
+ https://www.organic-chemistry.org/namedreactions/corey-winter-olefin-synthesis.shtm
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The Tsuji-Wilkinson decarbonylation reaction is a method for the decarbonylation of aldehydes and some acyl chlorides.
+
+ 2021-11-04T12:09:26Z
+ RXNO
+ RXNO:0000661
+ Tsuji-Wilkinson decarbonylation
+
+
+
+
+ The Tsuji-Wilkinson decarbonylation reaction is a method for the decarbonylation of aldehydes and some acyl chlorides.
+ https://dbpedia.org/page/Tsuji%E2%80%93Wilkinson_decarbonylation_reaction
+ Although decarbonylation can be effected by several transition metal complexes, Wilkinson's catalyst has proven the most effective.
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A chemical reaction in which ketones are synthesized from formaldehyde or other aldehydes, involving a temporary repolarization of a carbonyl group.
+
+ 2021-11-05T07:51:22Z
+ RXNO
+ Corey-Seebach Umpolung
+ Seebach Umpolung
+ RXNO:0000662
+ Corey-Seebach reaction
+
+
+
+
+ A chemical reaction in which ketones are synthesized from formaldehyde or other aldehydes, involving a temporary repolarization of a carbonyl group.
+ https://en.wikipedia.org/wiki/Corey-Seebach_reaction
+ https://www.organic-chemistry.org/namedreactions/corey-seebach-reaction.shtm
+ Usually, the aldehyde is first reacted with propane-1,3-dithiol to form a 1,3-dithiane, which then reacts with an electrophile after deprotonation with n-butyllithium.
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Nitroxide exchange reactions are based on thermal C–O bond homolysis of alkoxyamines, which leads to transient carbon-centred radicals and persistent nitroxide radicals. Usually these carbon centred radicals are quickly trapped by the nitroxide radicals and reform the alkoxyamines.
+
+ 2021-11-12T08:28:13Z
+ RXNO
+ RXNO:0000663
+ IUPAC does not recommend the use of the often synonymously used terms "nitroxyl radicals" or "nitroxides" for the class of "aminoxyl radicals".
+ nitroxide exchange reaction
+
+
+
+
+ Nitroxide exchange reactions are based on thermal C–O bond homolysis of alkoxyamines, which leads to transient carbon-centred radicals and persistent nitroxide radicals. Usually these carbon centred radicals are quickly trapped by the nitroxide radicals and reform the alkoxyamines.
+
+
+
+
+
+ IUPAC does not recommend the use of the often synonymously used terms "nitroxyl radicals" or "nitroxides" for the class of "aminoxyl radicals".
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The conversion of pyran or pyrone (pyranone) derivatives to the corresponding pyridine derivative.
+
+ 2021-11-12T09:25:38Z
+ RXNO
+ RXNO:0000664
+ Baeyer pyridine synthesis
+
+
+
+
+ The conversion of pyran or pyrone (pyranone) derivatives to the corresponding pyridine derivative.
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Oxidation of primary and secondary alcohols via their alkoxysulfonium salts. Upon the addition of base, the salt rearranges intramolecularly to aldehydes and ketones, respectively.
+
+ 2021-11-15T08:58:15Z
+ RXNO
+ Corey-Kim reaction
+ RXNO:0000665
+ Corey-Kim oxidation
+
+
+
+
+ Oxidation of primary and secondary alcohols via their alkoxysulfonium salts. Upon the addition of base, the salt rearranges intramolecularly to aldehydes and ketones, respectively.
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Oxidation of primary and secondary alcohols to aldehydes and ketones, respectively, through the use of pyridinium chlorochromate (PCC).
+
+ 2021-11-15T09:09:31Z
+ RXNO
+ PCC oxidation
+ RXNO:0000666
+ Corey-Suggs oxidation
+
+
+
+
+ Oxidation of primary and secondary alcohols to aldehydes and ketones, respectively, through the use of pyridinium chlorochromate (PCC).
+
+
+
+
+
+
+
+
+
+ Oxidation of primary and secondary alcohols to aldehydes and ketones, respectively, through the use of pyridinium dichromate (PDC).
+
+ 2021-11-15T09:20:03Z
+ RXNO
+ PDC oxidation
+ RXNO:0000667
+ Corey-Schmidt oxidation
+
+
+
+
+ Oxidation of primary and secondary alcohols to aldehydes and ketones, respectively, through the use of pyridinium dichromate (PDC).
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A particularly mild oxidation method in which, for example, dimethyl sulfoxide and acetic anhydride can be used as oxidizing agents to selectively produce aldehydes from primary alcohols without further oxidation to carboxylic acids. Analogously, secondary alcohols can be oxidized to form ketones.
+
+ 2021-11-15T09:30:47Z
+ RXNO
+ RXNO:0000668
+ Albright-Goldman oxidation
+
+
+
+
+ A particularly mild oxidation method in which, for example, dimethyl sulfoxide and acetic anhydride can be used as oxidizing agents to selectively produce aldehydes from primary alcohols without further oxidation to carboxylic acids. Analogously, secondary alcohols can be oxidized to form ketones.
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The Rubottom oxidation is a useful, high-yielding chemical reaction between silyl enol ethers and peroxy acids to give the corresponding α-hydroxy carbonyl product.
+
+ 2021-11-15T09:44:42Z
+ RXNO
+ Rubottom reaction
+ RXNO:0000669
+ Rubottom oxidation
+
+
+
+
+ The Rubottom oxidation is a useful, high-yielding chemical reaction between silyl enol ethers and peroxy acids to give the corresponding α-hydroxy carbonyl product.
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A three-component reaction (3CR) of a heterocyclic amidine, an aldehyde, and an isocyanide, resulting in a cyclic compound with imidazo[1,2-a] heterocycle as the core structure.
+
+ 2021-12-03T09:13:40Z
+ GBB reaction
+ GBB‐3CR reaction
+ RXNO
+ RXNO:0000670
+ Groebke-Blackburn-Bienaymé reaction
+
+
+
+
+ A three-component reaction (3CR) of a heterocyclic amidine, an aldehyde, and an isocyanide, resulting in a cyclic compound with imidazo[1,2-a] heterocycle as the core structure.
+ https://doi.org/10.1002/ejoc.201901124
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The preparation of oxindole/indolin-2-one from 2-nitrophenylacetic acid by reduction of the nitro group and subsequent dehydration.
+
+ 2021-12-03T14:20:07Z
+ RXNO
+ Baeyer indolinone synthesis
+ RXNO:0000671
+ Baeyer oxindole synthesis
+
+
+
+
+ The preparation of oxindole/indolin-2-one from 2-nitrophenylacetic acid by reduction of the nitro group and subsequent dehydration.
+ https://doi.org/10.1021/cr60118a003
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Condensation of a formamide acetal with a derivative of o-nitrotoluene to yield an enamine intermediate that subsequently undergoes reductive cyclization to give the corresponding indole.
+
+ 2021-12-03T14:45:01Z
+ Batcho-Leimgruber indole synthesis
+ RXNO
+ RXNO:0000672
+ Leimgruber-Batcho indole synthesis
+
+
+
+
+ Condensation of a formamide acetal with a derivative of o-nitrotoluene to yield an enamine intermediate that subsequently undergoes reductive cyclization to give the corresponding indole.
+ https://www.rsc.org/Merck-Index/reaction/r253/leimgruber-batcho%20indole%20synthesis
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Oxidation of alcohols to the corresponding carbonyl product using 2-iodoxybenzoic acid (IBX) as oxidizing agent.
+
+ 2021-11-15T11:24:35Z
+ RXNO
+ RXNO:0000673
+ IBX oxidation and Dess-Martin oxidation are alcohol oxidation by hypervalent iodine reagents. The Dess-Martin periodinane used for oxidation in the Dess-Martin oxidation is prepared by reacting IBX with acetic anhydride in DMSO.
+ IBX oxidation
+
+
+
+
+ Oxidation of alcohols to the corresponding carbonyl product using 2-iodoxybenzoic acid (IBX) as oxidizing agent.
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A chemical reaction in which a carboxylic acid (or its salt) reacts with an organic (alkyl or aryl) halide to form a new carbon-carbon bond with concomitant loss of CO2. In addition, the reaction requires a metal catalyst, a base and an oxidizing agent.
+
+ 2021-12-06T08:44:51Z
+ RXNO
+ RXNO:0000674
+ decarboxylative cross-coupling
+
+
+
+
+ A chemical reaction in which a carboxylic acid (or its salt) reacts with an organic (alkyl or aryl) halide to form a new carbon-carbon bond with concomitant loss of CO2. In addition, the reaction requires a metal catalyst, a base and an oxidizing agent.
+ https://en.wikipedia.org/wiki/Decarboxylative_cross-coupling
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A carbon-carbon coupling reaction between an arene and an alkene to give a substituted arene. The reaction is catalysed by a Lewis acid.
+
+ 2021-12-06T11:08:37Z
+ RXNO
+ RXNO:0000675
+ Balsohn alkylation
+
+
+
+
+ A carbon-carbon coupling reaction between an arene and an alkene to give a substituted arene. The reaction is catalysed by a Lewis acid.
+ https://second.wiki/wiki/balsohn-alkylierung
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A three-component condensation reaction in which primary or secondary amines react with a carbonyl compound (aldehyde or ketone) and a dialkyl phosphonate (also called dialkyl phosphite) to form an alpha-aminophosphonate.
+
+ 2021-12-13T11:39:08Z
+ RXNO
+ phospha-Mannich reaction
+ RXNO:0000676
+ Kabachnik-Fields reaction
+
+
+
+
+ A three-component condensation reaction in which primary or secondary amines react with a carbonyl compound (aldehyde or ketone) and a dialkyl phosphonate (also called dialkyl phosphite) to form an alpha-aminophosphonate.
+ https://doi.org/10.3390/molecules171112821
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A polymerisation reaction in which phenol and formaldehyde react together in a chain reaction to form a phenol formaldehyde resin (also infrequently called phenoplast).
+
+ 2021-12-13T12:52:17Z
+ RXNO
+ RXNO:0000677
+ Baekeland-Manasse-Lederer reaction
+
+
+
+
+ A polymerisation reaction in which phenol and formaldehyde react together in a chain reaction to form a phenol formaldehyde resin (also infrequently called phenoplast).
+ https://doi.org/10.1021/ie50003a004
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The rearrangement of an alpha-haloketone into an ester with a tertiary alpha-carbon atom by intramolecular migration of an alkyl or aryl group.
+
+ 2021-12-14T08:15:45Z
+ RXNO
+ RXNO:0000678
+ Aston-Greenburg rearrangement
+
+
+
+
+ The rearrangement of an alpha-haloketone into an ester with a tertiary alpha-carbon atom by intramolecular migration of an alkyl or aryl group.
+ https://doi.org/10.1021/ja01867a003
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The rearrangement/migration of alkyl groups in polyalkylbenzenes or polynuclear aromatic compounds in the presence of anhydrous aluminum chloride or the mixture of protonic acid and Lewis acid.
+
+ 2021-12-14T08:45:33Z
+ RXNO
+ RXNO:0000679
+ Baddeley isomerization
+
+
+
+
+ The rearrangement/migration of alkyl groups in polyalkylbenzenes or polynuclear aromatic compounds in the presence of anhydrous aluminum chloride or the mixture of protonic acid and Lewis acid.
+ https://doi.org/10.1002/9780470638859.conrr030
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The reduction of a thioester to an aldehyde by a silyl hydride in the presence of catalytic amounts of palladium.
+
+ 2021-12-14T09:43:52Z
+ RXNO
+ RXNO:0000680
+ Fukuyama reduction
+
+
+
+
+ The reduction of a thioester to an aldehyde by a silyl hydride in the presence of catalytic amounts of palladium.
+ https://en.wikipedia.org/wiki/Fukuyama_reduction
+ https://www.rsc.org/Merck-Index/reaction/r163/fukuyama%20reduction
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A three component cyclization of an aromatic or vinylic alkoxy pentacarbonyl chromium carbene complex, an alkyne and carbon monoxide to give a Cr(CO)3 coordinated phenol.
+
+ 2021-12-14T10:45:04Z
+ RXNO
+ Doetz reaction
+ Wulff-Dötz reaction
+ benzannulation reaction of Fischer carbene complexes
+ RXNO:0000681
+ Dötz reaction
+
+
+
+
+ A three component cyclization of an aromatic or vinylic alkoxy pentacarbonyl chromium carbene complex, an alkyne and carbon monoxide to give a Cr(CO)3 coordinated phenol.
+ https://en.wikipedia.org/wiki/Wulff%E2%80%93D%C3%B6tz_reaction
+ https://www.rsc.org/Merck-Index/reaction/r116/d%C3%B6tz%20reaction
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The formation of a substituted cyclopropanol by reaction of a carboxylic ester with a Grignard reagent (carrying a hydrogen atom in the beta-position) in the presence of a titanium(IV) alkoxide as catalyst. A modified cyclopropanol product can be generated by addition of a terminal alkene as a further reactant.
+
+ 2021-12-15T09:10:05Z
+ RXNO
+ RXNO:0000682
+ The dialkyldialkoxytitanium reagent, which actually reacts with the carboxylic ester, is generated in situ from the Grignard reagent and the titanium(IV) alkoxide.
+ Kulinkovich reaction
+
+
+
+
+ The formation of a substituted cyclopropanol by reaction of a carboxylic ester with a Grignard reagent (carrying a hydrogen atom in the beta-position) in the presence of a titanium(IV) alkoxide as catalyst. A modified cyclopropanol product can be generated by addition of a terminal alkene as a further reactant.
+ https://en.wikipedia.org/wiki/Kulinkovich_reaction
+ https://www.rsc.org/Merck-Index/reaction/r247/kulinkovich%20reaction
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The formation of a substituted cyclopropylamine by reaction of an amide with a Grignard reagent (carrying a hydrogen atom in the beta-position) in the presence of a titanium(IV) alkoxide as catalyst.
+
+ 2021-12-15T10:14:52Z
+ RXNO
+ RXNO:0000683
+ The Kulinkovich-de Meijere reaction is a modification of the Kulinkovich reaction (i.e., the reaction of an amide instead of a carboxylic ester under Kulinkovich conditions).
+ Kulinkovich-de Meijere reaction
+
+
+
+
+ The formation of a substituted cyclopropylamine by reaction of an amide with a Grignard reagent (carrying a hydrogen atom in the beta-position) in the presence of a titanium(IV) alkoxide as catalyst.
+ https://en.wikipedia.org/wiki/Kulinkovich_reaction
+ https://www.rsc.org/Merck-Index/reaction/r247/kulinkovich%20reaction
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The formation of a substituted primary cyclopropylamine by reaction of a nitrile with a Grignard reagent (carrying a hydrogen atom in the beta-position) in the presence of a titanium(IV) alkoxide as catalyst.
+
+ 2021-12-15T10:47:43Z
+ RXNO
+ RXNO:0000684
+ The Kulinkovich-Szymoniak reaction is a modification of the Kulinkovich reaction (i.e., the reaction of a nitrile instead of a carboxylic ester under Kulinkovich conditions).
+ Kulinkovich-Szymoniak reaction
+
+
+
+
+ The formation of a substituted primary cyclopropylamine by reaction of a nitrile with a Grignard reagent (carrying a hydrogen atom in the beta-position) in the presence of a titanium(IV) alkoxide as catalyst.
+ https://en.wikipedia.org/wiki/Kulinkovich_reaction
+ https://www.rsc.org/Merck-Index/reaction/r247/kulinkovich%20reaction
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Chiral (salen)manganese(III)-catalyzed asymmetric epoxidation of alkenes. In addition to the catalyst, stoichiometric amounts of an oxidant (e.g. sodium hypochlorite) are required.
+
+ 2021-12-16T08:34:02Z
+ RXNO
+ Jacobsen-Katsuki epoxidation
+ RXNO:0000686
+ Jacobsen epoxidation
+
+
+
+
+ Chiral (salen)manganese(III)-catalyzed asymmetric epoxidation of alkenes. In addition to the catalyst, stoichiometric amounts of an oxidant (e.g. sodium hypochlorite) are required.
+ https://en.wikipedia.org/wiki/Jacobsen_epoxidation
+ https://www.rsc.org/Merck-Index/reaction/r218/jacobsen%20epoxidation
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Organocatalytic enantioselective epoxidation of trans- and tri-substituted olefins using a fructose derived chiral ketone catalyst and potassium peroxomonosulfate or H2O2 as an oxidant.
+
+ 2021-12-16T08:57:48Z
+ RXNO
+ RXNO:0000687
+ Shi epoxidation
+
+
+
+
+ Organocatalytic enantioselective epoxidation of trans- and tri-substituted olefins using a fructose derived chiral ketone catalyst and potassium peroxomonosulfate or H2O2 as an oxidant.
+ https://www.rsc.org/Merck-Index/reaction/r399/shi%20epoxidation
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A multicomponent reaction (A-4CR) in which 3-thiazolines (2,5-dihydro-1,3-thiazoles) or mixtures of several 3-thiazolines are synthesized from elemental sulfur, an alpha-substitutable ketone or aldehyde, another carbonyl component and ammonia.
+
+ 2021-12-16T09:29:30Z
+ RXNO
+ Asinger thiazoline synthesis
+ Asinger-4 component reaction (A-4CR)
+ RXNO:0000688
+ Asinger reaction
+
+
+
+
+ A multicomponent reaction (A-4CR) in which 3-thiazolines (2,5-dihydro-1,3-thiazoles) or mixtures of several 3-thiazolines are synthesized from elemental sulfur, an alpha-substitutable ketone or aldehyde, another carbonyl component and ammonia.
+ https://doi.org/10.1002/cmdc.202100086
+ https://en.wikipedia.org/wiki/Asinger_reaction
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Cleavage of methyl ketones (i.e. oxidative demethylation) with halogens (or hypohalites) in the presence of a base to give a carboxylic acid and haloform (trihalomethane).
+
+ 2021-12-16T11:10:42Z
+ RXNO
+ Einhorn reaction
+ Lieben reaction
+ RXNO:0000689
+ haloform reaction
+
+
+
+
+ Cleavage of methyl ketones (i.e. oxidative demethylation) with halogens (or hypohalites) in the presence of a base to give a carboxylic acid and haloform (trihalomethane).
+ https://en.wikipedia.org/wiki/Haloform_reaction
+ https://www.rsc.org/Merck-Index/reaction/r257/lieben%20iodoform%20reaction
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ The conversion of dialkyl phosphites (dialkyl phosphonates) to dialkyl chlorophosphates using tetrachloromethane and a base (usually a primary, secondary or tertiary amine).
+
+ 2021-12-16T12:05:47Z
+ RXNO
+ AT reaction
+ RXNO:0000690
+ Since the dialkyl chlorophosphates formed are often too reactive to be isolated, conversion to the corresponding phosphate or phosphoramidate occurs in the presence of a suitable nucleophile (e.g., alcohol or amine) after the actual Atherton-Todd reaction.
+ Atherton-Todd reaction
+
+
+
+
+ The conversion of dialkyl phosphites (dialkyl phosphonates) to dialkyl chlorophosphates using tetrachloromethane and a base (usually a primary, secondary or tertiary amine).
+ https://doi.org/10.3762/bjoc.10.117
+ https://en.wikipedia.org/wiki/Atherton%E2%80%93Todd_reaction
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Synthesis of diarylmethane derivatives using an aldehyde and an aromatic compound at low temperature in an acidic medium.
+
+ 2021-12-16T12:54:23Z
+ RXNO
+ RXNO:0000691
+ A Friedel-Crafts type reaction proceeding via electrophilic aromatic substitution.
+ Baeyer diarylmethane synthesis
+
+
+
+
+ Synthesis of diarylmethane derivatives using an aldehyde and an aromatic compound at low temperature in an acidic medium.
+ https://doi.org/10.1016/B978-0-08-096630-4.00412-8
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ A hydroxyl group deprotection in which an silyl ether group is transformed into a hydroxy group.
+
+ 2021-12-16T13:23:35Z
+ RXNO
+ RXNO:0000692
+ silyl deprotection
+
+
+
+
+
+
+