Name Reactions

Alder ene reaction.- Aldol condensation.- Algar— Flynn— Oyamada Reaction.- Allan–Robinson reaction.- Arndt—Eistert homologation.- Baeyer–Villiger oxidation.- Baker–Venkataraman rearrangement.- Bamford–Stevens reaction.- Barbier coupling reaction.- Bartoli indole synthesis.- Barton radical decarboxylation.- Barton–McCombie deoxygenation.- Barton nitrite photolysis.- Batcho–Leimgruber indole synthesis.- Baylis–Hillman reaction.- Beckmann rearrangement.- Benzilic acid rearrangement.- Benzoin condensation.- Bergman cyclization.- Biginelli pyrimidone synthesis.- Birch reduction.- Bischler–Möhlau indole synthesis.- Bischler–Napieralski reaction.- Blaise reaction.- Blum–Ittah aziridine synthesis.- Boekelheide reaction.- Boger pyridine synthesis.- Borch reductive amination.- Borsche–Drechsel cyclizations.- Boulton–Katritzky rearrangement.- Bouveault aldehyde synthesis.- Bouveault—Blanc reduction.- Bradsher reaction.- Brook rearrangement.- Brown hydroboration.- Bucherer carbazole synthesis.- Bucherer reaction.- Bucherer—Bergs reaction.- Büchner ring expansion.- Buchwald–Hartwig amination.- Burgess reagent.- Burke boronates.- Cadiot–Chodkiewicz coupling.- Camps quinoline synthesis.- Cannizzaro reaction.- Carroll rearrangement.- Castro–Stephens coupling.- Chan alkyne reduction.- Chan–Lam C–X coupling reaction.- Chapman rearrangement.- Chichibabin pyridine synthesis.- Chugaev elimination.- Ciamician–Dennsted rearrangement.- Claisen condensation.- Claisen isoxazole synthesis.- Claisen rearrangements.- Clemmensen reduction.- Combes quinoline synthesis.- Conrad–Limpach reaction.- Cope elimination reaction.- Cope rearrangement.- Corey–Bakshi–Shibata (CBS) reagent.- Corey–Chaykovsky reaction.- Corey–Fuchs reaction.- Corey–Kim oxidation.- Corey–Nicolaou macrolactonization.- Corey–Seebach reaction.- Corey–Winter olefin synthesis.- Criegee glycol cleavage.- Criegee mechanism of ozonolysis.- Curtius rearrangement.- Dakin oxidation.- Dakin–West reaction.- Darzens condensation.- Delépine amine synthesis.- de Mayo reaction.- Demjanov rearrangement.- Dess–Martin periodinane oxidation.- Dieckmann condensation.- Diels–Alder reaction.- Dienone–phenol rearrangement.- Di–π–methane rearrangement.- Doebner quinoline synthesis.- Doebner–von Miller reaction.- Dötz reaction.- Dowd–Beckwith ring expansion.- Dudley reagent.- Erlenmeyer–Plöchl azlactone synthesis.- Eschenmoser's salt.- Eschenmoser–Tanabe fragmentation.- Eschweiler–Clarke reductive alkylation of amines.- Evans aldol reaction.- Favorskii rearrangement.- Feist–Bénary furan synthesis.- Ferrier carbocyclization.- Ferrier glycal allylic rearrangement.- Fiesselmann thiophene synthesis.- Fischer indole synthesis.- Fischer oxazole synthesis.- Fleming–Kumada oxidation.- Friedel–Crafts reaction.- Friedländer quinoline synthesis.- Fries rearrangement.- Fukuyama amine synthesis.- Fukuyama reduction.- Gabriel synthesis.- Gabriel–Colman rearrangement.- Gassman indole synthesis.- Gattermann–Koch reaction.- Gewald aminothiophene synthesis.- Glaser coupling.- Gomberg–Bachmann reaction.- Gould–Jacobs reaction.- Grignard reaction.- Grob fragmentation.- Guareschi–Thorpe condensation.- Hajos–Wiechert reaction.- Haller–Bauer reaction.- Hantzsch dihydropyridine synthesis.- Hantzsch pyrrole synthesis.- Heck reaction.- Hegedus indole synthesis.- Hell—Volhard—Zelinsky reaction.- Henry nitroaldol reaction.- Hinsberg synthesis of thiophene derivatives.- Hiyama cross-coupling reaction.- Hofmann rearrangement.- Hofmann–Löffler–Freytag reaction.- Horner—Wadsworth—Emmons reaction.- Houben–Hoesch reaction.- Hunsdiecker–Borodin reaction.- Jacobsen–Katsuki epoxidation.- Japp–Klingemann hydrazone synthesis.- Jones oxidation.- Julia–Kocienski olefination.- Julia–Lythgoe olefination.- Kahne glycosidation.- Knoevenagel condensation.- Knorr pyrazole synthesis.- Koch–Haaf carbonylation.- Koenig–Knorr glycosidation.- Kostanecki reaction.- Kröhnke pyridine synthesis.- Kumada cross-coupling reaction.- Lawesson's reagent.- Leuckart–Wallach reaction.- Lossen rearrangement.- McFadyen–Stevens reduction.- McMurry coupling.- Mannich reaction.- Martin's sulfurane dehydrating reagent.- Masamune–Roush conditions for the Horner–Emmons reaction.- Meerwein's salt.- Meerwein–Ponndorf–Verley reduction.- Meisenheimer complex.- [1,2]-Meisenheimer rearrangement.- [2,3]-Meisenheimer rearrangement.- Meyers oxazoline method.- Meyer–Schuster rearrangement.- Michael addition.- Michaelis–Arbuzov phosphonate synthesis.- Midland reduction.- Minisci reaction.- Mislow–Evans rearrangement.- Mitsunobu reaction.- Miyaura borylation.- Moffatt oxidation.- Morgan–Walls reaction.- Mori–Ban indole synthesis.- Mukaiyama aldol reaction.- Mukaiyama Michael addition.- Mukaiyama reagent.- Myers–Saito cyclization.- Nazarov cyclization.- Neber rearrangement.- Nef reaction.- Negishi cross-coupling reaction.- Nenitzescu indole synthesis.- Newman–Kwart rearrangement.- Nicholas reaction.- Nicolaou IBX dehydrogenation.- Noyori asymmetric hydrogenation.- Nozaki–Hiyama–Kishi reaction.- Nysted reagent.- Oppenauer oxidation.- Overman rearrangement.- Paal thiophene synthesis.- Paal–Knorr furan synthesis.- Paal–Knorr pyrrole synthesis.- Parham cyclization.- Passerini reaction.- Paternó–Büchi reaction.- Pauson–Khand reaction.- Payne rearrangement.- Pechmann coumarin synthesis.- Perkin reaction.- Petasis reaction.- Petasis reagent.- Peterson olefination.- Pictet–Gams isoquinoline synthesis.- Pictet–Spengler tetrahydroisoquinoline synthesis.- Pinacol rearrangement.- Pinner reaction.- Polonovski reaction.- Polonovski–Potier reaction.- Pomeranz–Fritsch reaction.- Prévost trans-dihydroxylation.- Prins reaction.- Pschorr cyclization.- Pummerer rearrangement.- Ramberg–Bäcklund reaction.- Reformatsky reaction.- Regitz diazo synthesis.- Reimer–Tiemann reaction.- Reissert reaction.- Reissert indole synthesis.- Ring-closing metathesis (RCM).- Ritter reaction.- Robinson annulation.- Robinson–Gabriel synthesis.- Robinson–Schöpf reaction.- Rosenmund reduction.- Rubottom oxidation.- Rupe rearrangement.- Saegusa oxidation.- Sakurai allylation reaction.- Sandmeyer reaction.- Schiemann reaction.- Schmidt rearrangement.- Schmidt's trichloroacetimidate glycosidation reaction.- Shapiro reaction.- Sharpless asymmetric amino-hydroxylation.- Sharpless asymmetric dihydroxylation.- Sharpless asymmetric epoxidation.- Sharpless olefin synthesis.- Simmons–Smith reaction.- Skraup quinoline synthesis.- Smiles rearrangement.- Sommelet reaction.- Sommelet–Hauser rearrangement.- Sonogashira reaction.- Staudinger ketene cycloaddition.- Staudinger reduction.- Stetter reaction.- Still–Gennari phosphonate reaction.- Stille coupling.- Stille–Kelly reaction.- Stobbe condensation.- Strecker amino acid synthesis.- Suzuki–Miyaura coupling.- Swern oxidation.- Takai reaction.- Tebbe's reagent.- TEMPO oxidation.- Thorpe–Ziegler reaction.- Tsuji–Trost reaction.- Ugi reaction.- Ullmann coupling.- van Leusen oxazole synthesis.- Vilsmeier– Haack reaction.- Vinylcyclopropane–cyclopentene rearrangement.- von Braun reaction.- Wacker oxidation.- Wagner–Meerwein rearrangement.- Weiss–Cook reaction.- Wharton reaction.- White Reagent.- Willgerodt–Kindler reaction.- Wittig reaction.- [1,2]-Wittig rearrangement.- [2,3]-Wittig rearrangement.- Wohl–Ziegler reaction.- Wolff rearrangement.- Wolff–Kishner reduction.- Woodward cis-dihydroxylation.- Yamaguchi esterification.- Zincke reaction.