RXNO Ontology

The RXNO Ontology is a formal ontology of chemical named reactions.[1] [2] It was originally developed at the Royal Society of Chemistry (RSC) and is associated with the Open Biomedical Ontologies Foundry. The RXNO ontology unifies several previous attempts to systematize chemical reactions including the Merck Index and the hierarchy of Carey, Laffan, Thomson and Williams.[3][4]

Major Reaction Categories

The twelve top-level reaction categories proposed by Carey, Laffan, Thompson and Williams are given in the table below, together with their RXNO ontology identifiers and the equivalent wikipedia categories where applicable.[3]

IndexReaction CategoryRXNO IDWikipedia Category
1Heteroatom alkylation and arylationCategory:Carbon-heteroatom bond forming reactions
2Acylation and related processes
3Carbon-Carbon bond formationRXNO:0000002Category:Carbon-carbon bond forming reactions
4Heterocycle forming reactionsRXNO:0000349Category:Heterocycle forming reactions
5Protection reactionsRXNO:0000078
6Deprotection reactionsRXNO:0000203
7ReductionsCategory:Organic reduction reactions
8OxidationsCategory:Organic oxidation reactions
9Functional group interconversion (FGI)RXNO:0000011Category:Substitution reactions
10Functional group addition (FGA)
11Resolution reactions
12MiscellaneousCategory:Organic reactions

Name Reactions

The following table lists the RXNO identifiers for some example name reactions.

RXNO:0000003 Perkin reaction
RNXO:0000006 Diels–Alder reaction
RXNO:0000014 Grignard reaction
RXNO:0000015 Wittig reaction
RXNO:0000021 Sandmeyer reaction
RXNO:0000024 Heck reaction
RXNO:0000026 Beckmann rearrangement
RXNO:0000028 Cope rearrangement
RXNO:0000031 Baeyer–Villiger oxidation
RXNO:0000042 Birch reduction
RXNO:0000043 Claisen condensation
RXNO:0000056 Horner–Wadsworth–Emmons reaction
RXNO:0000062 Skraup reaction
RXNO:0000064 Fischer indole synthesis
RXNO:0000074 Wurtz reaction
RXNO:0000081 Ullmann condensation
RXNO:0000084 Barbier reaction
RXNO:0000088 Negishi coupling
RXNO:0000090 Williamson ether synthesis
RXNO:0000098 Glaser coupling
RXNO:0000103 Gabriel synthesis
RXNO:0000106 Hunsdiecker reaction
RXNO:0000140 Suzuki reaction
RXNO:0000147 Emde degradation
RXNO:0000148 Claisen rearrangement
RXNO:0000156 Lossen rearrangement
RXNO:0000157 Nef reaction
RXNO:0000183 Perkow reaction
RXNO:0000193 Hiyama coupling
RXNO:0000210 Fleming–Tamao oxidation
RXNO:0000218 Cannizzaro reaction
RXNO:0000288 Rosenmund–von Braun reaction
RXNO:0000369 Friedel–Crafts reaction
RXNO:0000444 Fries rearrangement
RXNO:0000550 Collins oxidation


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gollark: They are!
gollark: When they get "summoned", some xenowyrms come in and run some fancy special effects, then put in a fancy purple-painted egg, and when it grows up they wear a trenchcoat and do GoN stuff.
gollark: The hatchling form is really cool, huh.
gollark: As we all know, xenowyrms summon all new CB eggs. All hail xenowyrms.

See also

References

  1. Schneider, Nadine; Lowe, Daniel; Sayle, Roger; Tarselli, Michael; Landrum, Gregory (2016). "Big Data from Pharmaceutical Patents: A Computational Analysis of Medicinal Chemists' Bread and Butter". J. Med. Chem. 59 (9): 4385–4402. doi:10.1021/acs.jmedchem.6b00153. PMID 27028220.
  2. Schneider, Nadine; Lowe, Daniel; Sayle, Roger; Landrum, Gregory (Jan 2015). "Development of a Novel Fingerprint for Chemical Reactions and its Application to Large-Scale Reaction Classification and Similarity". Journal of Chemical Information and Modeling. 55: 39–53. doi:10.1021/ci5006614. PMID 25541888.
  3. Carey, JS; Laffan, D; Thomson, C; Williams, MT (May 2006). "Analysis of the reactions used for the preparation of drug candidate molecules". Organic & Biomolecular Chemistry. 4: 2337–2347. doi:10.1039/B602413K. PMID 16763676.
  4. Roughley, Stephen D.; Jordan, Allan M. (May 2011). "The Medicinal Chemist's Toolbox: An analysis of reactions used in the pursuit of drug candidates". Journal of Medicinal Chemistry. 54: 3451–79. doi:10.1021/jm200187y. PMID 21504168.
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