User:Amitosh.swain/Books/Reactions of Organic Chemistry (Name Reactions)
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Reactions of Organic Chemistry
[edit]Name Reactions
[edit]- 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