- 1,2-Wittig rearrangement
- Achmatowicz reaction
- Adkins-Peterson reaction
- Akabori amino acid reaction
- Aldol-Tishchenko reaction
- Algar-Flynn-Oyamada reaction
- Allan-Robinson reaction
- Amadori rearrangement
- Andrussow oxidation
- Angeli-Rimini reaction
- Appel reaction
- Arndt-Eistert synthesis
- Asinger reaction
- Auwers synthesis
- Aza Diels-Alder reaction
- Aza-Baylis-Hillman reaction
- Azide alkyne Huisgen cycloaddition
- Baeyer-Drewson indigo synthesis
- Baeyer-Villiger oxidation
- Baker-Venkataraman rearrangement
- Bamberger rearrangement
- Bamberger triazine synthesis
- Bamford-Stevens reaction
- Banert cascade
- Barbier reaction
- Bartoli indole synthesis
- Barton reaction
- Barton-Kellogg reaction
- Barton-McCombie deoxygenation
- Baudisch reaction
- Baylis-Hillman reaction
- Bechamp Reduction
- Bechamp reaction
- Beckmann rearrangement
- Benary reaction
- Bergman cyclization
- Bergmann degradation
- Bernthsen acridine synthesis
- Betti reaction
- Biginelli reaction
- Bingel reaction
- Birch reduction
- Bischler-Möhlau indole synthesis
- Bischler-Napieralski reaction
- Blaise ketone synthesis
- Blaise reaction
- Blanc chloromethylation
- Bodroux-Chichibabin aldehyde synthesis
- Boord olefin synthesis
- Bosch reaction
- Boudouard reaction
- Bouveault aldehyde synthesis
- Bouveault-Blanc reduction
- Boyland-Sims oxidation
- Brook rearrangement
- Bucherer carbazole synthesis
- Bucherer reaction
- Bucherer-Bergs reaction
- Buchwald-Hartwig reaction
- CBS reduction
- Cadiot-Chodkiewicz coupling
- Camps quinoline synthesis
- Cannizzaro reaction
- Carroll rearrangement
- Castro-Stephens coupling
- Chan rearrangement
- Chichibabin pyridine synthesis
- Chichibabin reaction
- Chugaev elimination
- Claisen condensation
- Claisen rearrangement
- Clemmensen reduction
- Combes quinoline synthesis
- Conrad-Limpach synthesis
- Cook-Heilbron thiazole synthesis
- Cope reaction
- Cope rearrangement
- Corey-Fuchs reaction
- Corey-House synthesis
- Corey-Kim oxidation
- Corey-Winter olefin synthesis
- Criegee rearrangement
- Curtius rearrangement
- Dakin reaction
- Dakin-West reaction
- Darzens reaction
- Delépine reaction
- Demjanov rearrangement
- Dess-Martin oxidation
- Diels-Alder reaction
- Dimroth rearrangement
- Doebner reaction
- Doebner-Miller reaction
- Dowd-Beckwith ring expansion reaction
- Duff reaction
- Dötz reaction
- Edman degradation
- Einhorn-Brunner reaction
- Elbs persulfate oxidation
- Emde degradation
- Erlenmeyer-Plöchl azlactone and amino acid synthesis
- Eschenmoser fragmentation
- Eschweiler-Clarke reaction
- Favorskii reaction
- Favorskii rearrangement
- Feist-Benary synthesis
- Ferrier rearrangement
- Finkelstein reaction
- Fischer esterification
- Fischer glycosidation
- Fischer indole synthesis
- Fischer oxazole synthesis
- Fischer-Hepp rearrangement
- Fleming-Tamao oxidation
- Forster-Decker method
- Friedel-Crafts reaction
- Friedländer synthesis
- Fries rearrangement
- Fritsch-Buttenberg-Wiechell rearrangement
- Fujimoto-Belleau reaction
- Fukuyama coupling
- Fukuyama indole synthesis
- Gabriel synthesis
- Gabriel-Colman rearrangement
- Gassman indole synthesis
- Gattermann reaction
- Gattermann-Koch reaction
- Gewald reaction
- Goldberg reaction
- Gomberg-Bachmann reaction
- Gould-Jacobs reaction
- Grieco elimination
- Grignard reaction
- Grob fragmentation
- Guerbet reaction
- Hajos-Parrish-Eder-Sauer-Wiechert reaction
- Hammick reaction
- Hantzsch pyridine synthesis
- Hantzsch pyrrole synthesis
- Hayashi rearrangement
- Heck reaction
- Hell-Volhard-Zelinsky halogenation
- Hemetsberger indole synthesis
- Herz reaction
- Hiyama coupling
- Hofmann elimination
- Hofmann rearrangement
- Hofmann-Löffler reaction
- Hofmann-Martius rearrangement
- Horner-Wadsworth-Emmons reaction
- Hunsdiecker reaction
- Hösch reaction
- Ireland-Claisen rearrangement
- Ivanov reaction
- Jacobsen epoxidation
- Jacobsen rearrangement
- Japp-Klingemann reaction
- Johnson-Corey-Chaykovsky reaction
- Jones oxidation
- Julia olefination
- Kiliani-Fischer synthesis
- Knoevenagel condensation
- Knorr pyrrole synthesis
- Knorr quinoline synthesis
- Koch reaction
- Kochi reaction
- Koenigs–Knorr reaction
- Kolbe electrolysis
- Kolbe nitrile synthesis
- Kolbe-Schmitt reaction
- Kornblum oxidation
- Kornblum–DeLaMare rearrangement
- Kowalski ester homologation
- Krapcho decarboxylation
- Kulinkovich reaction
- Kumada coupling
- Larock indole synthesis
- Lehmstedt-Tanasescu reaction
- Leimgruber-Batcho indole synthesis
- Lemieux-Johnson oxidation
- Letts nitrile synthesis
- Leuckart reaction
- Lobry-de Bruyn-van Ekenstein transformation
- Lossen rearrangement
- Luche reduction
- Madelung synthesis
- Mannich reaction
- Martinet dioxindole synthesis
- McFadyen-Stevens reaction
- McLafferty rearrangement
- McMurry reaction
- Meerwein arylation
- Meerwein-Ponndorf-Verley reduction
- Menshutkin reaction
- Meyer-Schuster rearrangement
- Meyers synthesis
- Michael reaction
- Michaelis-Arbuzov reaction
- Milas hydroxylation
- Mitsunobu reaction
- Mukaiyama aldol addition
- Mumm rearrangement
- Nazarov cyclization reaction
- Neber rearrangement
- Nef reaction
- Negishi coupling
- Nenitzescu indole synthesis
- Nicholas reaction
- Niementowski quinazoline synthesis
- Niementowski quinoline synthesis
- Nierenstein reaction
- Norrish reaction
- Noyori asymmetric hydrogenation
- Nozaki-Hiyama-Kishi Nickel/Chromium Coupling reaction
- Oppenauer oxidation
- Overman rearrangement
- Paal-Knorr synthesis
- Passerini reaction
- Paterno-Buchi reaction
- Pauson–Khand reaction
- Pechmann condensation
- Pellizzari reaction
- Perkin reaction
- Perkow reaction
- Petasis reaction
- Peterson olefination
- Pfitzinger reaction
- Pfitzner-Moffatt oxidation
- Pictet-Spengler reaction
- Pinner reaction
- Povarov reaction
- Prato reaction
- Prins reaction
- Prévost reaction
- Pummerer rearrangement
- Ramberg-Bäcklund reaction
- Rauhut-Currier reaction
- Reed reaction
- Reformatsky reaction
- Reimer-Tiemann reaction
- Reissert indole synthesis
- Reissert reaction
- Riemschneider thiocarbamate synthesis
- Ritter reaction
- Robinson annulation
- Robinson-Gabriel synthesis
- Rosenmund reduction
- Rosenmund-von Braun synthesis
- Rubottom oxidation
- Rupe reaction
- Ruzicka large ring synthesis
- Sakurai reaction
- Sandmeyer reaction
- Sarett oxidation
- Schiemann reaction
- Schmidt reaction
- Scholl reaction
- Schotten-Baumann reaction
- Seyferth-Gilbert homologation
- Shapiro reaction
- Sharpless asymmetric dihydroxylation
- Sharpless epoxidation
- Sharpless oxyamination
- Shi epoxidation
- Simmons-Smith reaction
- Skattebøl rearrangement
- Skraup reaction
- Smiles rearrangement
- Sommelet reaction
- Sonogashira coupling
- Staudinger reaction
- Stephen aldehyde synthesis
- Stetter reaction
- Stevens rearrangement
- Stieglitz rearrangement
- Stille reaction
- Stollé synthesis
- Stork enamine alkylation
- Strecker amino acid synthesis
- Suzuki reaction
- Swern oxidation
- Takai olefination
- Thorpe reaction
- Tiffeneau-Demjanov rearrangement
- Tishchenko reaction
- Trost asymmetric allylic alkylation
- Ugi reaction
- Ullmann condensation
- Ullmann reaction
- Upjohn dihydroxylation
- Urech hydantoin synthesis
- Varrentrapp reaction
- Vilsmeier-Haack reaction
- Volhard-Erdmann cyclization
- Von Braun amide degradation
- Von Braun reaction
- Von Richter reaction
- Wacker process
- Wagner-Jauregg reaction
- Wagner-Meerwein rearrangement
- Wallach rearrangement
- Weerman degradation
- Weinreb ketone synthesis
- Wenker synthesis
- Westphalen-Lettré rearrangement
- Wharton reaction
- Whiting reaction
- Willgerodt rearrangement
- Williamson ether synthesis
- Wittig reaction
- Wohl degradation
- Wohl-Aue reaction
- Wohl-Ziegler reaction
- Wolff rearrangement
- Wolff-Kishner reduction
- Wolffenstein-Böters reaction
- Woodward cis-hydroxylation
- Wurtz reaction
- Wurtz-Fittig reaction
- Wöhler synthesis
- Zincke reaction
- Zincke-Suhl reaction
- Zinke nitration
- Étard reaction
