Name Reactions

Alder ene reaction.- Aldol condensation.- Algar#x2014; Flynn#x2014; Oyamada Reaction.- Allan#x2013;Robinson reaction.- Arndt#x2014;Eistert homologation.- Baeyer#x2013;Villiger oxidation.- Baker#x2013;Venkataraman rearrangement.- Bamford#x2013;Stevens reaction.- Barbier coupling reaction.- Bartoli indole synthesis.- Barton radical decarboxylation.- Barton#x2013;McCombie deoxygenation.- Barton nitrite photolysis.- Batcho#x2013;Leimgruber indole synthesis.- Baylis#x2013;Hillman reaction.- Beckmann rearrangement.- Benzilic acid rearrangement.- Benzoin condensation.- Bergman cyclization.- Biginelli pyrimidone synthesis.- Birch reduction.- Bischler#x2013;M#x00F6;hlau indole synthesis.- Bischler#x2013;Napieralski reaction.- Blaise reaction.- Blum#x2013;Ittah aziridine synthesis.- Boekelheide reaction.- Boger pyridine synthesis.- Borch reductive amination.- Borsche#x2013;Drechsel cyclizations.- Boulton#x2013;Katritzky rearrangement.- Bouveault aldehyde synthesis.- Bouveault#x2014;Blanc reduction.- Bradsher reaction.- Brook rearrangement.- Brown hydroboration.- Bucherer carbazole synthesis.- Bucherer reaction.- Bucherer#x2014;Bergs reaction.- B#x00FC;chner ring expansion.- Buchwald#x2013;Hartwig amination.- Burgess reagent.- Burke boronates.- Cadiot#x2013;Chodkiewicz coupling.- Camps quinoline synthesis.- Cannizzaro reaction.- Carroll rearrangement.- Castro#x2013;Stephens coupling.- Chan alkyne reduction.- Chan#x2013;Lam C#x2013;X coupling reaction.- Chapman rearrangement.- Chichibabin pyridine synthesis.- Chugaev elimination.- Ciamician#x2013;Dennsted rearrangement.- Claisen condensation.- Claisen isoxazole synthesis.- Claisen rearrangements.- Clemmensen reduction.- Combes quinoline synthesis.- Conrad#x2013;Limpach reaction.- Cope elimination reaction.- Cope rearrangement.- Corey#x2013;Bakshi#x2013;Shibata (CBS) reagent.- Corey#x2013;Chaykovsky reaction.- Corey#x2013;Fuchs reaction.- Corey#x2013;Kim oxidation.- Corey#x2013;Nicolaou macrolactonization.- Corey#x2013;Seebach reaction.- Corey#x2013;Winter olefin synthesis.- Criegee glycol cleavage.- Criegee mechanism of ozonolysis.- Curtius rearrangement.- Dakin oxidation.- Dakin#x2013;West reaction.- Darzens condensation.- Del#x00E9;pine amine synthesis.- de Mayo reaction.- Demjanov rearrangement.- Dess#x2013;Martin periodinane oxidation.- Dieckmann condensation.- Diels#x2013;Alder reaction.- Dienone#x2013;phenol rearrangement.- Di#x2013;#x03C0;#x2013;methane rearrangement.- Doebner quinoline synthesis.- Doebner#x2013;von Miller reaction.- D#x00F6;tz reaction.- Dowd#x2013;Beckwith ring expansion.- Dudley reagent.- Erlenmeyer#x2013;Pl#x00F6;chl azlactone synthesis.- Eschenmoser#x2019;s salt.- Eschenmoser#x2013;Tanabe fragmentation.- Eschweiler#x2013;Clarke reductive alkylation of amines.- Evans aldol reaction.- Favorskii rearrangement.- Feist#x2013;B#x00E9;nary furan synthesis.- Ferrier carbocyclization.- Ferrier glycal allylic rearrangement.- Fiesselmann thiophene synthesis.- Fischer indole synthesis.- Fischer oxazole synthesis.- Fleming#x2013;Kumada oxidation.- Friedel#x2013;Crafts reaction.- Friedl#x00E4;nder quinoline synthesis.- Fries rearrangement.- Fukuyama amine synthesis.- Fukuyama reduction.- Gabriel synthesis.- Gabriel#x2013;Colman rearrangement.- Gassman indole synthesis.- Gattermann#x2013;Koch reaction.- Gewald aminothiophene synthesis.- Glaser coupling.- Gomberg#x2013;Bachmann reaction.- Gould#x2013;Jacobs reaction.- Grignard reaction.- Grob fragmentation.- Guareschi#x2013;Thorpe condensation.- Hajos#x2013;Wiechert reaction.- Haller#x2013;Bauer reaction.- Hantzsch dihydropyridine synthesis.- Hantzsch pyrrole synthesis.- Heck reaction.- Hegedus indole synthesis.- Hell#x2014;Volhard#x2014;Zelinsky reaction.- Henry nitroaldol reaction.- Hinsberg synthesis of thiophene derivatives.- Hiyama cross-coupling reaction.- Hofmann rearrangement.- Hofmann#x2013;L#x00F6;ffler#x2013;Freytag reaction.- Horner#x2014;Wadsworth#x2014;Emmons reaction.- Houben#x2013;Hoesch reaction.- Hunsdiecker#x2013;Borodin reaction.- Jacobsen#x2013;Katsuki epoxidation.- Japp#x2013;Klingemann hydrazone synthesis.- Jones oxidation.- Julia#x2013;Kocienski olefination.- Julia#x2013;Lythgoe olefination.- Kahne glycosidation.- Knoevenagel condensation.- Knorr pyrazole synthesis.- Koch#x2013;Haaf carbonylation.- Koenig#x2013;Knorr glycosidation.- Kostanecki reaction.- Kr#x000F6;hnke pyridine synthesis.- Kumada cross-coupling reaction.- Lawesson#x2019;s reagent.- Leuckart#x2013;Wallach reaction.- Lossen rearrangement.- McFadyen#x2013;Stevens reduction.- McMurry coupling.- Mannich reaction.- Martin#x2019;s sulfurane dehydrating reagent.- Masamune#x2013;Roush conditions for the Horner#x2013;Emmons reaction.- Meerwein#x2019;s salt.- Meerwein#x2013;Ponndorf#x2013;Verley reduction.- Meisenheimer complex.- [1,2]-Meisenheimer rearrangement.- [2,3]-Meisenheimer rearrangement.- Meyers oxazoline method.- Meyer#x2013;Schuster rearrangement.- Michael addition.- Michaelis#x2013;Arbuzov phosphonate synthesis.- Midland reduction.- Minisci reaction.- Mislow#x2013;Evans rearrangement.- Mitsunobu reaction.- Miyaura borylation.- Moffatt oxidation.- Morgan#x2013;Walls reaction.- Mori#x2013;Ban indole synthesis.- Mukaiyama aldol reaction.- Mukaiyama Michael addition.- Mukaiyama reagent.- Myers#x2013;Saito cyclization.- Nazarov cyclization.- Neber rearrangement.- Nef reaction.- Negishi cross-coupling reaction.- Nenitzescu indole synthesis.- Newman#x2013;Kwart rearrangement.- Nicholas reaction.- Nicolaou IBX dehydrogenation.- Noyori asymmetric hydrogenation.- Nozaki#x2013;Hiyama#x2013;Kishi reaction.- Nysted reagent.- Oppenauer oxidation.- Overman rearrangement.- Paal thiophene synthesis.- Paal#x2013;Knorr furan synthesis.- Paal#x2013;Knorr pyrrole synthesis.- Parham cyclization.- Passerini reaction.- Patern#x00F3;#x2013;B#x00FC;chi reaction.- Pauson#x2013;Khand reaction.- Payne rearrangement.- Pechmann coumarin synthesis.- Perkin reaction.- Petasis reaction.- Petasis reagent.- Peterson olefination.- Pictet#x2013;Gams isoquinoline synthesis.- Pictet#x2013;Spengler tetrahydroisoquinoline synthesis.- Pinacol rearrangement.- Pinner reaction.- Polonovski reaction.- Polonovski#x2013;Potier reaction.- Pomeranz#x2013;Fritsch reaction.- Pr#x00E9;vost trans-dihydroxylation.- Prins reaction.- Pschorr cyclization.- Pummerer rearrangement.- Ramberg#x2013;B#x00E4;cklund reaction.- Reformatsky reaction.- Regitz diazo synthesis.- Reimer#x2013;Tiemann reaction.- Reissert reaction.- Reissert indole synthesis.- Ring-closing metathesis (RCM).- Ritter reaction.- Robinson annulation.- Robinson#x2013;Gabriel synthesis.- Robinson#x2013;Sch#x00F6;pf reaction.- Rosenmund reduction.- Rubottom oxidation.- Rupe rearrangement.- Saegusa oxidation.- Sakurai allylation reaction.- Sandmeyer reaction.- Schiemann reaction.- Schmidt rearrangement.- Schmidt#x2019;s trichloroacetimidate glycosidation reaction.- Shapiro reaction.- Sharpless asymmetric amino-hydroxylation.- Sharpless asymmetric dihydroxylation.- Sharpless asymmetric epoxidation.- Sharpless olefin synthesis.- Simmons#x2013;Smith reaction.- Skraup quinoline synthesis.- Smiles rearrangement.- Sommelet reaction.- Sommelet#x2013;Hauser rearrangement.- Sonogashira reaction.- Staudinger ketene cycloaddition.- Staudinger reduction.- Stetter reaction.- Still#x2013;Gennari phosphonate reaction.- Stille coupling.- Stille#x2013;Kelly reaction.- Stobbe condensation.- Strecker amino acid synthesis.- Suzuki#x2013;Miyaura coupling.- Swern oxidation.- Takai reaction.- Tebbe#x2019;s reagent.- TEMPO oxidation.- Thorpe#x2013;Ziegler reaction.- Tsuji#x2013;Trost reaction.- Ugi reaction.- Ullmann coupling.- van Leusen oxazole synthesis.- Vilsmeier#x2013; Haack reaction.- Vinylcyclopropane#x2013;cyclopentene rearrangement.- von Braun reaction.- Wacker oxidation.- Wagner#x2013;Meerwein rearrangement.- Weiss#x2013;Cook reaction.- Wharton reaction.- White Reagent.- Willgerodt#x2013;Kindler reaction.- Wittig reaction.- [1,2]-Wittig rearrangement.- [2,3]-Wittig rearrangement.- Wohl#x2013;Ziegler reaction.- Wolff rearrangement.- Wolff#x2013;Kishner reduction.- Woodward cis-dihydroxylation.- Yamaguchi esterification.- Zincke reaction.