User:Physchim62/Ontologies

This is based on the RSC Name Reactions Ontology, a hierarchy of classes of organic chemical reactions.

Cleaving reaction

 * Beckmann fragmentation
 * Criegee oxidation
 * Dakin reaction
 * Edman degradation
 * Emde degradation
 * Japp–Klingemann reaction
 * Retro-aldol addition

End-of-chain shortening

 * Barbier–Wieland degradation
 * Barton decarboxylation
 * Hunsdiecker reaction
 * Schmidt rearrangement, carboxylic acid
 * Strecker degradation
 * Weerman reaction

Extrusion reaction

 * Benzidine rearrangement
 * Ramberg–Bäcklund reaction
 * Semidine rearrangement

Fragmentation reaction

 * Grob rearrangement

Polonovski reaction

 * Polonovski reaction
 * Polonovski–Potier reaction

Functional modification

 * Deprotection reaction

Addition reaction

 * Birch reduction
 * Hydroamination
 * Hydroboration
 * Hydroboration–oxidation
 * Hydrosilylation
 * Noyori asymmetric hydrogenation, alkene
 * Sharpless asymmetric aminohydroxylation
 * Sharpless asymmetric dihydroxylation
 * Stork–Crabtree hydrogenation

Hydrometallation

 * Hydroalumination
 * Hydrostannylation
 * Hydrotelluration
 * Hydrozirconation

Elimination reaction

 * Bamford–Stevens reaction
 * Hofmann elimination
 * Shapiro reaction

Functional group modification

 * Aza–Wittig reaction
 * Azo coupling
 * Cannizzaro reaction
 * Crossed Cannizzaro reaction
 * Finkelstein reaction
 * Leukart reaction
 * Leukart–Wallart reaction
 * Nef reaction
 * Pummerer reaction
 * Ritter reaction
 * Sommelet reaction
 * Tishchenko reaction
 * Willgerodt reaction
 * Willgerodt–Kindler reaction
 * Woehler reaction

Functional group oxidation

 * Dess–Martin oxidation
 * Diazotisation
 * Elbs persulfate oxidation, tolyl varient
 * Fenton reaction, carboxylic acid varient
 * Fenton reaction, diol varient
 * Fetizon oxidation
 * Lindgren oxidation
 * Menshutkin reaction
 * Oppenauer oxidation
 * Pfitzner–Moffatt oxidation
 * Swern oxidation
 * Wacker process
 * Wacker–Tsuji oxidation

Functional group reduction

 * Barton–McCombie deoxygenation
 * Bouveault–Blanc reaction
 * Clemmensen reduction
 * Luche reduction
 * Meerwein–Ponndorf–Verley reduction
 * Noyori asymmetric hydrogenation, carbonyl
 * Rosenmund reduction
 * Wolff–Kishner reduction
 * Wolff–Kishner reduction, Huang–Minlon modification
 * Zemplen transesterification

Protection reaction

 * Boc protection
 * Fmoc protection

Substitution reaction

 * Allylic rearrangement
 * Arbuzov reaction
 * Fischer–Speier esterification
 * Fleming–Tamao oxidation
 * Gabriel synthesis
 * Ing–Manske procedure
 * Katritzky pyrylium–pyridinium method
 * Kharasch–Sosnovsky reaction
 * Michaelis–Arbuzov reaction
 * Nicholas reaction, nucleophilic heteroatom centre
 * Petasis reaction
 * Schotten–Baumann reaction
 * Tamao oxidation
 * Williamson ether synthesis
 * Wohl–Ziegler bromination

Aromatic substitution

 * Balz–Schiemann reaction
 * Boyland–Sims oxidation
 * Buchwald–Hartwig amination
 * Elbs persulfate oxidation, phenol variant
 * Gattermann halogenation
 * Goldberg reaction
 * Koerner–Contardi reaction
 * Sandmeyer reaction
 * Ullmann condensation

Mitsunobu reaction

 * Bose–Mitsunobu reaction
 * Mitsunobu reaction

Joining reaction

 * Aza–ene reaction
 * Dakin–West reaction
 * Ene reaction
 * Fischer–Tropsch process
 * Hydroformylation
 * Passerini reaction
 * Perkow reaction
 * Staudinger reaction
 * Thiol–ene reaction
 * Ugi reaction
 * Vorbrueggen condensation

Carbon–carbon coupling reaction

 * Acyloin condensation
 * Aza–Henry reaction
 * Barbier reaction
 * Benzoin condensation
 * Blaise reaction
 * Cadiot–Chodkiewicz coupling
 * Cadogan coupling
 * Cativa process
 * Claisen condensation
 * Friedel–Crafts acylation
 * Friedel–Crafts alkylation
 * Gattermann reaction
 * Grignard reaction
 * Heck reaction
 * Henry reaction
 * Hiyama coupling
 * Horner reaction
 * Horner–Wadsworth–Emmons reaction
 * Julia olefination
 * Knoevenagel condensation
 * Kolbe electrolysis
 * Kolbe–Schmitt reaction
 * Kumada coupling
 * Luche reaction
 * Malonic ester synthesis
 * Mannich reaction
 * Monsanto process
 * Negishi coupling
 * Nicholas reaction, nucleophilic carbon centre
 * Nozaki–Hiyama–Kishi reaction
 * Peterson olefination
 * Prins reaction
 * Reimer–Tiemann reaction
 * Rosenmund–von Braun reaction
 * Sakurai reaction, acetal or ketal
 * Sakurai reaction, acid chloride
 * Sakurai reaction, aldehyde or ketone
 * Sakurai reaction, enone
 * Sakurai reaction, iminium salt
 * Sonogashira coupling
 * Stille coupling
 * Stork–Wittig olefination
 * Suzuki–Miyaura coupling
 * Vilsmeier–Haack reaction
 * Zimmermann reaction

Aldol addition

 * Aldol condensation

Baylis–Hillman reaction

 * Baylis–Hillman reaction
 * Aza–Baylis–Hillman reaction

Carbon–carbon homocoupling reaction

 * Eglinton reaction
 * Glaser coupling
 * Ullmann reaction
 * Wurtz reaction
 * Zweifel diene synthesis

Hydrovinylation

 * 1,4-Hydrovinylation

Reformatsky reaction

 * Reformatsky reaction
 * Imino Reformatsky reaction

Wittig reaction

 * Wittig reaction
 * Wittig methylenation

Chain lengthening

 * Corey–Fuchs reaction
 * Kharasch reaction
 * Strecker reaction

Conjugate addition

 * Michael addition
 * Nitro–Michael reaction

Insertion reaction

 * Arndt–Eistert reaction
 * Baeyer–Villiger oxidation
 * Schmidt rearrangement, alkene
 * Schmidt rearrangement, ketone
 * Schmidt rearrangement, tertiary alcohol

Joining with rearrangement

 * Bellus–Claisen rearrangement
 * Eschenmoser–Claisen rearrangement
 * Johnson–Claisen rearrangement

Multiple-bond metathesis

 * Alkene metathesis
 * Alkyne metathesis
 * Enyne metathesis

Polymerisation reaction

 * Aufbau reaction
 * Ring-opening metathesis polymerisation
 * Yamamoto polymerisation

Rearrangement

 * Aromatic Claisen rearrangement
 * Aza–Ferrier rearrangement
 * Baker–Venkataraman rearrangement
 * Barton reaction
 * Beckmann rearrangement
 * Benzilic acid rearrangement
 * Brook rearrangement
 * Carroll rearrangement
 * Claisen rearrangement
 * Cope rearrangement
 * Curtius rearrangement
 * Ferrier rearrangement
 * Fischer–Hepp rearrangement
 * Fritsch–Buttenberg–Wiechell rearrangement
 * Ireland–Claisen rearrangement
 * Lossen rearrangement
 * Metalla–aza–Claisen rearrangement
 * Neber rearrangement
 * Oxy–Cope rearrangement
 * Pinacol rearrangement
 * Sommelet–Hauser rearrangement
 * Steglich rearrangement
 * Wolff rearrangement

Aza–Cope rearrangement

 * 1-aza–Cope rearrangement
 * 2-aza–Cope rearrangement
 * 3-aza–Cope rearrangement

Stevens rearrangement

 * Stevens rearrangement, ammonium
 * Stevens rearrangement, sulfonium

Wittig rearrangement

 * 1,2-aza–Wittig rearrangement
 * 1,2-Wittig rearrangement
 * 2,3-aza–Wittig rearrangement
 * 2,3-Wittig rearrangement

Ring breaking

 * Retro Diels–Alder reaction
 * Ring-opening metathesis
 * Sakurai reaction, epoxide

Ring expansion

 * Pfitzinger reaction

Ring formation reaction

 * 1,3-Dipolar cycloaddition
 * Alkyne–azide click reaction
 * Bergman cyclisation
 * Biginelli reaction
 * Copper(I)-catalyzed azide–alkyne cycloaddition
 * Darzens reaction
 * Dieckmann cyclisation
 * Hantzsch pyridine synthesis
 * Intramolecular Prins reaction
 * Nazarov cyclisation
 * Paterno–Buchi reaction
 * Ring-closing enyne metathesis
 * Ring-closing metathesis
 * Sharpless asymmetric epoxidation
 * Simmons–Smith reaction

Diels–Alder reaction

 * Diels–Alder reaction
 * Aza–Diels–Alder reaction

Fused-ring-system formation

 * Bischler–Napieralski reaction
 * Cadogan carbazole synthesis
 * Doebner reaction
 * Doebner–Miller reaction
 * Fischer indole synthesis
 * MacDonald condensation
 * Pictet–Spengler reaction
 * Skraup reaction

Paal–Knorr synthesis

 * Paal–Knorr furan synthesis
 * Paal–Knorr pyrrole synthesis
 * Paal–Knorr thiophene synthesis

Ring rearrangement

 * Achmatowicz rearrangement
 * Aza–Achmatowicz rearrangement
 * Aza–Payne rearrangement
 * Dimroth rearrangement
 * Payne rearrangement