User:Drpundir/Books/Organic Name Reactions
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Organic Name Reactions
[edit]Reaction and Mechanism
[edit]- Introduction
- Name reaction
- Name Reactions
- 1,2-Wittig rearrangement
- Achmatowicz reaction
- Adkins-Peterson reaction
- Akabori amino acid 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
- Auwers synthesis
- Aza Diels-Alder reaction
- Aza-Baylis–Hillman reaction
- Azide alkyne Huisgen cycloaddition
- Baeyer-Drewson indigo synthesis
- Baeyer-Emmerling indole synthesis
- Baeyer–Villiger oxidation
- Baker–Venkataraman rearrangement
- Balz–Schiemann reaction
- 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 Zard Synthesis
- Barton-Kellogg reaction
- Barton–McCombie deoxygenation
- 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
- Bray–Liebhafsky reaction
- Briggs–Rauscher reaction
- Brook rearrangement
- Bucherer carbazole synthesis
- Bucherer reaction
- Bucherer–Bergs reaction
- Buchwald–Hartwig amination
- Cadiot-Chodkiewicz coupling
- Camps quinoline synthesis
- Cannizzaro reaction
- Carroll rearrangement
- Castro-Stephens coupling
- Chan rearrangement
- Chapman rearrangement
- Chichibabin pyridine synthesis
- Chichibabin reaction
- Chugaev elimination
- Claisen condensation
- Claisen rearrangement
- Clemmensen reduction
- Combes quinoline synthesis
- Conrad-Limpach synthesis
- Cook-Heilbron thiazole synthesis
- Cope reaction
- Cope rearrangement
- Corey-Fuchs reaction
- Corey-House synthesis
- Corey-Itsuno reduction
- Corey-Winter olefin synthesis
- Corey–Kim oxidation
- Criegee rearrangement
- Curtius rearrangement
- Dakin oxidation
- Dakin–West reaction
- Danheiser annulation
- Darzens reaction
- Debus-Radziszewski imidazole synthesis
- Delépine reaction
- Demjanov rearrangement
- Dess–Martin periodinane
- Diels–Alder reaction
- Dimroth rearrangement
- Doebner reaction
- Doebner–Miller reaction
- Dowd–Beckwith ring expansion 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
- Favorskii reaction
- Favorskii rearrangement
- Feist-Benary synthesis
- Ferrier carbocyclization
- Ferrier rearrangement
- Finkelstein reaction
- Fischer glycosidation
- Fischer indole synthesis
- Fischer oxazole synthesis
- Fischer–Hepp rearrangement
- Fischer–Speier esterification
- Fleming–Tamao oxidation
- Forster-Decker method
- 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
- Gattermann–Koch reaction
- Gewald reaction
- Girdler sulfide process
- 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
- Hantzsch pyrrole 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
- Intramolecular Diels-Alder cycloaddition
- Ireland–Claisen rearrangement
- Isay reaction
- Ivanov reaction
- Jacobsen epoxidation
- Jacobsen rearrangement
- Japp-Maitland condensation
- Japp–Klingemann reaction
- Johnson–Corey–Chaykovsky reaction
- Jones oxidation
- Julia olefination
- Juliá-Colonna epoxidation
- Kabachnik–Fields reaction
- Kauffmann olefination
- Kharasch addition
- Kiliani–Fischer synthesis
- 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
- 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
- Liebeskind-Srogl coupling
- Lindgren oxidation
- Lobry–de Bruyn–van Ekenstein transformation
- Lossen rearrangement
- Luche reduction
- 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
- Meyers synthesis
- Meyer–Schuster rearrangement
- Michael reaction
- Michaelis–Arbuzov reaction
- Michaelis–Becker reaction
- Midland Alpine Borane Reduction
- Milas hydroxylation
- Mitsunobu reaction
- Mukaiyama aldol addition
- Mumm rearrangement
- 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
- Noyori asymmetric hydrogenation
- 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–Spengler reaction
- Pinner reaction
- Pinnick oxidation
- Povarov reaction
- Prato reaction
- Prins reaction
- Prévost reaction
- Pummerer rearrangement
- Ramberg–Bäcklund reaction
- Rauhut–Currier reaction
- Reed reaction
- Reformatsky reaction
- Reilly-Hickinbottom rearrangement
- Reimer–Tiemann reaction
- Reissert indole synthesis
- Reissert reaction
- Retro-Diels–Alder reaction
- 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
- Schikorr reaction
- Schmidt reaction
- Scholl reaction
- Schotten–Baumann reaction
- Schöllkopf method
- 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
- Stieglitz rearrangement
- Stille reaction
- Stollé synthesis
- Stork enamine alkylation
- Strecker amino acid synthesis
- Strecker degradation
- Suzuki reaction
- Swern oxidation
- Takai olefination
- 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
- User:Goblueium/Jones Oxidation Before Editing
- User:Goblueium/Jones' Reagent SSG Draft
- User:ILoveAndrew734/sandbox
- User:Jkolev/sandbox
- User:MorningSnack/sandbox
- User:UmichSSGleader/History
- User:UmichSSGleader/M history
- Van den Bergh reaction
- Varrentrapp reaction
- 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
- Willgerodt rearrangement
- Williamson ether synthesis
- Wittig reaction
- Wohl degradation
- Wohl-Aue reaction
- Wohl–Ziegler bromination
- Wolff rearrangement
- Wolffenstein-Böters reaction
- Wolff–Kishner reduction
- Woodward cis-hydroxylation
- Wulff-Dötz reaction
- Wurtz reaction
- Wurtz-Fittig reaction
- Wöhler synthesis
- Yamaguchi esterification
- Zincke aldehyde
- Zincke nitration
- Zincke reaction
- Zincke-Suhl reaction
- Zinin reaction
- Metathesis
- Alkane metathesis
- Alkyne metathesis
- Olefin metathesis
- Salt metathesis reaction
- Ziegler–Natta catalyst
- Chemical process
- Monsanto process
- Pechiney–Ugine–Kuhlmann process
- Shell higher olefin process