User:Amitosh.swain/Books/Reactions of Organic Chemistry (Name Reactions)

Name Reactions

 * Name reaction
 * 1,2-Wittig rearrangement
 * 2,3-Wittig rearrangement
 * Abramov reaction
 * Achmatowicz reaction
 * Adams decarboxylation
 * Adkins–Peterson reaction
 * Akabori amino-acid reaction
 * Alder ene reaction
 * Aldol–Tishchenko reaction
 * Algar–Flynn–Oyamada reaction
 * Allan–Robinson reaction
 * Amadori rearrangement
 * Andrussow process
 * Angeli–Rimini reaction
 * Appel reaction
 * Arndt–Eistert reaction
 * Asinger reaction
 * Asymmetric Keck allylation
 * Auwers synthesis
 * Aza-Baylis–Hillman reaction
 * Aza-Cope rearrangement
 * Aza-Diels–Alder reaction
 * Azide-alkyne Huisgen cycloaddition
 * Baeyer–Drewson indigo synthesis
 * Baeyer–Emmerling indole synthesis
 * Baeyer–Villiger oxidation
 * Baker–Venkataraman rearrangement
 * Bamberger rearrangement
 * Bamberger triazine synthesis
 * Bamford–Stevens reaction
 * Banert cascade
 * Barbier reaction
 * Bardhan–Senguph phenanthrene synthesis
 * Bartoli indole synthesis
 * Barton decarboxylation
 * Barton reaction
 * Barton vinyl iodine procedure
 * Barton–Kellogg reaction
 * Barton–McCombie deoxygenation
 * Barton–Zard reaction
 * Baudisch reaction
 * Baylis–Hillman reaction
 * Bechamp reaction
 * Bechamp reduction
 * Beckmann rearrangement
 * Belousov–Zhabotinsky reaction
 * Benary reaction
 * Benkeser reaction
 * Bergman cyclization
 * Bergmann azlactone peptide synthesis
 * Bergmann degradation
 * Bernthsen acridine synthesis
 * Betti reaction
 * Biginelli reaction
 * Bingel reaction
 * Birch reduction
 * Birkeland–Eyde process
 * Bischler–Möhlau indole synthesis
 * Bischler–Napieralski reaction
 * Blaise ketone synthesis
 * Blaise reaction
 * Blanc chloromethylation
 * Bodroux reaction
 * Bodroux–Chichibabin aldehyde synthesis
 * Bohn–Schmidt reaction
 * Boord olefin synthesis
 * Borodin reaction
 * Borsche-Drechsel cyclization
 * Bosch reaction
 * Boudouard reaction
 * Bouveault aldehyde synthesis
 * Bouveault–Blanc reduction
 * Boyland–Sims oxidation
 * Bradsher cycloaddition
 * Bray–Liebhafsky reaction
 * Briggs–Rauscher reaction
 * Brook rearrangement
 * Bucherer carbazole synthesis
 * Bucherer reaction
 * Bucherer–Bergs reaction
 * Buchner ring expansion
 * Buchwald–Hartwig amination
 * Cadiot–Chodkiewicz coupling
 * Camps quinoline synthesis
 * Cannizzaro reaction
 * Carroll rearrangement
 * Castro–Stephens coupling
 * Chan rearrangement
 * Chapman rearrangement
 * Chichibabin pyridine synthesis
 * Chugaev elimination
 * Claisen condensation
 * Claisen rearrangement
 * Clemmensen reduction
 * Combes quinoline synthesis
 * Conrad–Limpach synthesis
 * Cook–Heilbron thiazole synthesis
 * Cope reaction
 * Cope rearrangement
 * Corey-Chaykovsky reagent
 * Corey–Fuchs reaction
 * Corey–House synthesis
 * Corey–Itsuno reduction
 * Corey–Kim oxidation
 * Corey–Winter olefin synthesis
 * Creighton process
 * Criegee rearrangement
 * Curtius rearrangement
 * Dakin oxidation
 * Dakin–West reaction
 * Danheiser annulation
 * Darzens reaction
 * Darzens tetralin synthesis
 * Debus-Radziszewski imidazole synthesis
 * Delépine reaction
 * Demjanov rearrangement
 * Dess–Martin periodinane
 * Devarda's alloy
 * Diels–Alder reaction
 * Diels–Reese reaction
 * Dimroth rearrangement
 * Doebner reaction
 * Doebner–Miller reaction
 * Dötz reaction
 * Wulff–Dötz reaction
 * Dowd–Beckwith ring-expansion reaction
 * Doyle–Kirmse reaction
 * Duff reaction
 * Edman degradation
 * Einhorn–Brunner reaction
 * Elbs persulfate oxidation
 * Elbs reaction
 * Emde degradation
 * Erlenmeyer–Plöchl azlactone and amino-acid synthesis
 * Eschenmoser fragmentation
 * Eschenmoser sulfide contraction
 * Eschweiler–Clarke reaction
 * Evans–Saksena reduction
 * Evans–Tishchenko reaction
 * Favorskii reaction
 * Favorskii rearrangement
 * Feist–Benary synthesis
 * Ferrier carbocyclization
 * Ferrier rearrangement
 * Fétizon oxidation
 * Finkelstein reaction
 * Fischer assay
 * Fischer–Speier esterification
 * Fischer glycosidation
 * Fischer indole synthesis
 * Fischer oxazole synthesis
 * Fischer–Hepp rearrangement
 * Fleming–Tamao oxidation
 * Forster–Decker method
 * Fráter–Seebach alkylation
 * Freund reaction
 * Friedel–Crafts reaction
 * Friedländer synthesis
 * Fries rearrangement
 * Fritsch–Buttenberg–Wiechell rearrangement
 * Fujimoto–Belleau reaction
 * Fukuyama coupling
 * Fukuyama indole synthesis
 * Fukuyama reduction
 * Gabriel synthesis
 * Gabriel–Colman rearrangement
 * Gallagher–Hollander degradation
 * Gassman indole synthesis
 * Gattermann reaction
 * Gewald reaction
 * Girdler sulfide process
 * Goldberg reaction
 * Gomberg–Bachmann reaction
 * Gould–Jacobs reaction
 * Grieco elimination
 * Grignard reaction
 * Grob fragmentation
 * Grundmann aldehyde synthesis
 * Guerbet reaction
 * Haber–Weiss reaction
 * Hajos–Parrish–Eder–Sauer–Wiechert reaction
 * Haller-Bauer reaction
 * Hammick reaction
 * Hantzsch pyridine synthesis
 * Haworth Phenanthrene synthesis
 * Hayashi rearrangement
 * Heck reaction
 * Heck–Matsuda reaction
 * Hell–Volhard–Zelinsky halogenation
 * Hemetsberger indole synthesis
 * Henry reaction
 * Herz reaction
 * Hinsberg oxindole synthesis
 * Hiyama coupling
 * Hoesch reaction
 * Hofmann elimination
 * Hofmann rearrangement
 * Hofmann–Löffler reaction
 * Hooker reaction
 * Horner–Wadsworth–Emmons reaction
 * Hunsdiecker reaction
 * Imine Diels–Alder reaction
 * Intramolecular Diels–Alder cycloaddition
 * Ireland–Claisen rearrangement
 * Isay reaction
 * Ivanov reaction
 * Jacobsen epoxidation
 * Jacobsen rearrangement
 * Japp–Klingemann reaction
 * Japp–Maitland condensation
 * Johnson–Corey–Chaykovsky reaction
 * Jones oxidation
 * Julia olefination
 * Juliá–Colonna epoxidation
 * Kabachnik–Fields reaction
 * Kauffmann olefination
 * Kharasch addition
 * Kiliani–Fischer synthesis
 * Kirsanov reaction
 * Kishner cyclopropane 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
 * Kostanecki acylation
 * Kowalski ester homologation
 * Krapcho decarboxylation
 * Kulinkovich reaction
 * Kumada coupling
 * Larock indole synthesis
 * Lectka enantioselective beta-lactam synthesis
 * Lehmstedt–Tanasescu reaction
 * Leimgruber–Batcho indole synthesis
 * Lemieux–Johnson oxidation
 * Letts nitrile synthesis
 * Leuckart reaction
 * Ley Oxidation
 * Liebeskind–Srogl coupling
 * Lindgren oxidation
 * Lobry de Bruyn–van Ekenstein transformation
 * Lossen rearrangement
 * Luche reduction
 * Lumière–Barbier method
 * Madelung synthesis
 * Maillard reaction
 * Mannich reaction
 * Marker degradation
 * Markó–Lam deoxygenation
 * Marschalk reaction
 * Marsh test
 * Martinet dioxindole synthesis
 * McCormack reaction
 * McFadyen–Stevens reaction
 * McLafferty rearrangement
 * McMurry reaction
 * Meerwein arylation
 * Meerwein–Ponndorf–Verley reduction
 * Menshutkin reaction
 * Meyer synthesis
 * Meyer–Schuster rearrangement
 * Meyers synthesis
 * Michael reaction
 * Michaelis–Arbuzov reaction
 * Michaelis–Becker reaction
 * Midland Alpine borane reduction
 * Milas hydroxylation
 * Minisci reaction
 * Mislow–Evans rearrangement
 * Mitsunobu reaction
 * Mozingo reduction
 * Mukaiyama aldol addition
 * Mumm rearrangement
 * Nametkin rearrangement
 * Narasaka–Prasad reduction
 * Nazarov cyclization reaction
 * Neber rearrangement
 * Nef reaction
 * Negishi coupling
 * Nenitzescu indole synthesis
 * Newman–Kwart rearrangement
 * Nicholas reaction
 * Niementowski quinazoline synthesis
 * Niementowski quinoline synthesis
 * Nierenstein reaction
 * Norrish reaction
 * Nozaki–Hiyama–Kishi reaction
 * Oppenauer oxidation
 * Overman rearrangement
 * Paal–Knorr synthesis
 * Parikh–Doering oxidation
 * Passerini reaction
 * Paternò–Büchi reaction
 * Pauson–Khand reaction
 * Pechmann condensation
 * Pellizzari reaction
 * Perkin reaction
 * Perkow reaction
 * Petasis reaction
 * Peterson olefination
 * Petrenko-Kritschenko piperidone synthesis
 * Pfitzinger reaction
 * Pfitzner–Moffatt oxidation
 * Piancatelli rearrangement
 * Pictet–Hubert reaction
 * Pictet–Spengler reaction
 * Pinner reaction
 * Pinnick oxidation
 * Pomeranz–Fritsch reaction
 * Povarov reaction
 * Prato reaction
 * Prévost reaction
 * Prins reaction
 * Pummerer rearrangement
 * Quelet reaction
 * Ramberg–Bäcklund reaction
 * Rauhut–Currier reaction
 * Jaffe reaction
 * Reed reaction
 * Reformatsky reaction
 * Reilly–Hickinbottom rearrangement
 * Reimer–Tiemann reaction
 * Reissert indole synthesis
 * Reissert reaction
 * Reppe synthesis
 * Retro-Diels–Alder reaction
 * Retropinacol rearrangement
 * Riemschneider thiocarbamate synthesis
 * Ritter reaction
 * Robinson annulation
 * Robinson–Gabriel synthesis
 * Rosenmund reduction
 * Rosenmund–von Braun reaction
 * Rubottom oxidation
 * Ruff degradation
 * Ruzicka large-ring synthesis
 * Saegusa–Ito oxidation
 * Sakurai reaction
 * Salol reaction
 * Sandmeyer reaction
 * Sarett oxidation
 * Saville reaction
 * Balz–Schiemann reaction
 * Schikorr reaction
 * Schmidt reaction
 * Scholl reaction
 * Schöllkopf method
 * 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
 * Soai reaction
 * Sommelet reaction
 * Sonogashira coupling
 * Staudinger reaction
 * Staudinger synthesis
 * Steglich esterification
 * Stephen aldehyde synthesis
 * Stetter reaction
 * Stevens rearrangement
 * Stickland fermentation
 * Stieglitz rearrangement
 * Stille reaction
 * Stollé synthesis
 * Stork enamine alkylation
 * Strecker amino-acid synthesis
 * Strecker degradation
 * Suzuki reaction
 * Swarts fluorination
 * Swern oxidation
 * Takai olefination
 * Ter Meer reaction
 * Thorpe reaction
 * Tiemann rearrangement
 * Tiffeneau–Demjanov rearrangement
 * Tipson–Cohen reaction
 * Tishchenko reaction
 * Tsuji–Trost reaction
 * Ugi reaction
 * Ullmann condensation
 * Ullmann reaction
 * Upjohn dihydroxylation
 * Urech hydantoin synthesis
 * Van den Bergh reaction
 * Van Leusen reaction
 * Varrentrapp reaction
 * Vicarious nucleophilic substitution
 * 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 degradation
 * Wallach rearrangement
 * Weerman degradation
 * Weidel's reaction
 * Weinreb ketone synthesis
 * Wenker synthesis
 * Westphalen–Lettré rearrangement
 * Wharton reaction
 * Whiting reaction
 * Widman–Stoermer synthesis
 * Willgerodt rearrangement
 * Williamson ether synthesis
 * Wittig reaction
 * Wohl degradation
 * Wohl–Aue reaction
 * Wohl–Ziegler bromination
 * Wöhler synthesis
 * Wolff rearrangement
 * Wolff–Kishner reduction
 * Wolffenstein–Böters reaction
 * Woodward cis-hydroxylation
 * Wurtz reaction
 * Wurtz–Fittig reaction
 * Yamaguchi esterification
 * Zincke nitration
 * Zincke reaction
 * Zincke–Suhl reaction
 * Zinin reaction