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

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Reactions of Organic Chemistry

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Name Reactions

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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