User:Physchim62/Ontologies
This is based on the RSC Name Reactions Ontology, a hierarchy of classes of organic chemical reactions.
Cleaving reaction[edit]
- Beckmann fragmentation
- Criegee oxidation
- Dakin reaction
- Edman degradation
- Emde degradation
- Japp–Klingemann reaction
- Retro-aldol addition
End-of-chain shortening[edit]
- Barbier–Wieland degradation
- Barton decarboxylation
- Hunsdiecker reaction
- Schmidt rearrangement, carboxylic acid
- Strecker degradation
- Weerman reaction
Extrusion reaction[edit]
Fragmentation reaction[edit]
Polonovski reaction[edit]
Functional modification[edit]
Addition reaction[edit]
- Birch reduction
- Hydroamination
- Hydroboration
- Hydroboration–oxidation
- Hydrosilylation
- Noyori asymmetric hydrogenation, alkene
- Sharpless asymmetric aminohydroxylation
- Sharpless asymmetric dihydroxylation
- Stork–Crabtree hydrogenation
Hydrometallation[edit]
Elimination reaction[edit]
Functional group modification[edit]
- 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[edit]
- 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[edit]
- 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[edit]
Substitution reaction[edit]
- 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[edit]
- 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[edit]
Joining reaction[edit]
- 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[edit]
- 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[edit]
Baylis–Hillman reaction[edit]
Carbon–carbon homocoupling reaction[edit]
Hydrovinylation[edit]
Reformatsky reaction[edit]
Wittig reaction[edit]
Chain lengthening[edit]
Conjugate addition[edit]
Insertion reaction[edit]
- Arndt–Eistert reaction
- Baeyer–Villiger oxidation
- Schmidt rearrangement, alkene
- Schmidt rearrangement, ketone
- Schmidt rearrangement, tertiary alcohol
Joining with rearrangement[edit]
Multiple-bond metathesis[edit]
Polymerisation reaction[edit]
Rearrangement[edit]
- 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[edit]
Stevens rearrangement[edit]
- Stevens rearrangement, ammonium
- Stevens rearrangement, sulfonium
Wittig rearrangement[edit]
- 1,2-aza–Wittig rearrangement
- 1,2-Wittig rearrangement
- 2,3-aza–Wittig rearrangement
- 2,3-Wittig rearrangement
Ring breaking[edit]
Ring contraction[edit]
Ring expansion[edit]
Ring formation reaction[edit]
- 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[edit]
Fused-ring-system formation[edit]
- Bischler–Napieralski reaction
- Cadogan carbazole synthesis
- Doebner reaction
- Doebner–Miller reaction
- Fischer indole synthesis
- MacDonald condensation
- Pictet–Spengler reaction
- Skraup reaction