Name reactions

Source: Wikipedia. Pages: 204. Chapters: Swern oxidation, Sharpless epoxidation, Diels-Alder reaction, Pinner reaction, Sharpless asymmetric dihydroxylation, Nazarov cyclization reaction, Birch reduction, Juliá-Colonna epoxidation, Wittig reaction, Hajos-Parrish-Eder-Sauer-Wiechert reaction, Grignard reaction, Johnson-Corey-Chaykovsky reaction, Tiffeneau-Demjanov rearrangement, Marker degradation, Friedel-Crafts reaction, Schikorr reaction, Briggs-Rauscher reaction, Azide alkyne Huisgen cycloaddition, Ugi reaction, Dakin oxidation, Meerwein-Ponndorf-Verley reduction, Maillard reaction, Michael reaction, Heck reaction, Petasis reaction, Paal-Knorr synthesis, Corey-Itsuno reduction, Weinreb ketone synthesis, Dess-Martin periodinane, Marsh test, Oppenauer oxidation, Wacker process, Pictet-Spengler reaction, Pinnick oxidation, Zincke aldehyde, Saegusa-Ito oxidation, Fischer-Speier esterification, Chichibabin pyridine synthesis, Claisen rearrangement, Zincke reaction, Retro-Diels-Alder reaction, Knorr pyrrole synthesis, Baeyer-Villiger oxidation, Horner-Wadsworth-Emmons reaction, Beckmann rearrangement, Baylis-Hillman reaction, Stille reaction, Arndt-Eistert reaction, Mitsunobu reaction, Belousov-Zhabotinsky reaction, Kumada coupling, Prins reaction, Sonogashira coupling, Negishi coupling, Meyer-Schuster rearrangement, Kulinkovich reaction, Jacobsen epoxidation, Mannich reaction, Suzuki reaction, Barton-McCombie deoxygenation, Simmons-Smith reaction, Buchwald-Hartwig amination, Bucherer-Bergs reaction, Ullmann condensation, Ferrier rearrangement, Bischler-Napieralski reaction, Prato reaction, Ferrier carbocyclization, Robinson annulation, Darzens reaction, Peterson olefination, Wulff-Dötz reaction, Tsuji-Trost reaction, Williamson ether synthesis, McMurry reaction, Bartoli indole synthesis, Sandmeyer reaction, Fries rearrangement, Claisen condensation, Knoevenagel condensation, Ramberg-Bäcklund reaction, Julia olefination, Tipson-Cohen reaction, Grob fragmentation, Mukaiyama aldol addition, Schmidt reaction, Norrish reaction, Bingel reaction, Cope rearrangement, Wöhler synthesis, Michaelis-Arbuzov reaction, Seyferth-Gilbert homologation, Gabriel synthesis, Strecker amino acid synthesis, Cadiot-Chodkiewicz coupling, Brook rearrangement, Cannizzaro reaction, Povarov reaction, Wurtz reaction, Favorskii rearrangement, Nozaki-Hiyama-Kishi reaction, Biginelli reaction, Pummerer rearrangement, Leimgruber-Batcho indole synthesis, Carroll rearrangement, Staudinger reaction, Nef reaction, Ullmann reaction, Corey-Kim oxidation, Barton decarboxylation, Kiliani-Fischer synthesis, Petrenko-Kritschenko piperidone synthesis, Bergman cyclization, Pauson-Khand reaction, Kornblum-DeLaMare rearrangement, Reformatsky reaction, Jones oxidation, Sakurai reaction, Doebner-Miller reaction, Hunsdiecker reaction, Japp-Klingemann reaction, Shapiro reaction, Bray-Liebhafsky reaction, Curtius rearrangement, Vilsmeier-Haack reaction, Barbier reaction, Parikh-Doering oxidation, Aza-Baylis-Hillman reaction, Gomberg-Bachmann reaction, Stetter reaction, Wolff rearrangement, Heck-Matsuda Reaction, Meerwein arylation, Passerini reaction, Girdler sulfide process, Bamberger rearrangement, Perkow reaction, Boudouard reaction, Finkelstein reaction, Eschenmoser fragmentation, Schotten-Baumann reaction, Dowd-Beckwith ring expansion reaction, Hell-Volhard-Zelinsky halogenation, Rauhut-Currier reaction, Guerbet reaction, Baker-Venkataraman rearrangement, Edman degradation, Achmatowicz ...