User:Itub/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 oxidation
 * Angeli-Rimini reaction
 * Appel reaction
 * Arndt-Eistert synthesis
 * Asinger reaction
 * Auwers synthesis
 * Aza Diels-Alder reaction
 * Aza-Baylis-Hillman reaction
 * Azide alkyne Huisgen cycloaddition
 * Baeyer-Drewson indigo synthesis
 * Baeyer-Villiger oxidation
 * Baker-Venkataraman rearrangement
 * Bamberger rearrangement
 * Bamberger triazine synthesis
 * Bamford-Stevens reaction
 * Banert cascade
 * Barbier reaction
 * Bartoli indole synthesis
 * Barton reaction
 * Barton-Kellogg reaction
 * Barton-McCombie deoxygenation
 * Baudisch reaction
 * Baylis-Hillman reaction
 * Bechamp Reduction
 * Bechamp reaction
 * Beckmann rearrangement
 * Benary reaction
 * Bergman cyclization
 * Bergmann degradation
 * Bernthsen acridine synthesis
 * Betti reaction
 * Biginelli reaction
 * Bingel reaction
 * Birch reduction
 * Bischler-Möhlau indole synthesis
 * Bischler-Napieralski reaction
 * Blaise ketone synthesis
 * Blaise reaction
 * Blanc chloromethylation
 * Bodroux-Chichibabin aldehyde synthesis
 * Boord olefin synthesis
 * Bosch reaction
 * Boudouard reaction
 * Bouveault aldehyde synthesis
 * Bouveault-Blanc reduction
 * Boyland-Sims oxidation
 * Brook rearrangement
 * Bucherer carbazole synthesis
 * Bucherer reaction
 * Bucherer-Bergs reaction
 * Buchwald-Hartwig reaction
 * CBS reduction
 * Cadiot-Chodkiewicz coupling
 * Camps quinoline synthesis
 * Cannizzaro reaction
 * Carroll rearrangement
 * Castro-Stephens coupling
 * Chan 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-Kim oxidation
 * Corey-Winter olefin synthesis
 * Criegee rearrangement
 * Curtius rearrangement
 * Dakin reaction
 * Dakin-West reaction
 * Darzens reaction
 * Delépine reaction
 * Demjanov rearrangement
 * Dess-Martin oxidation
 * Diels-Alder reaction
 * Dimroth rearrangement
 * Doebner reaction
 * Doebner-Miller reaction
 * Dowd-Beckwith ring expansion reaction
 * Duff reaction
 * Dötz reaction
 * Edman degradation
 * Einhorn-Brunner reaction
 * Elbs persulfate oxidation
 * Emde degradation
 * Erlenmeyer-Plöchl azlactone and amino acid synthesis
 * Eschenmoser fragmentation
 * Eschweiler-Clarke reaction
 * Favorskii reaction
 * Favorskii rearrangement
 * Feist-Benary synthesis
 * Ferrier rearrangement
 * Finkelstein reaction
 * Fischer esterification
 * Fischer glycosidation
 * Fischer indole synthesis
 * Fischer oxazole synthesis
 * Fischer-Hepp rearrangement
 * Fleming-Tamao oxidation
 * Forster-Decker method
 * Friedel-Crafts reaction
 * Friedländer synthesis
 * Fries rearrangement
 * Fritsch-Buttenberg-Wiechell rearrangement
 * Fujimoto-Belleau reaction
 * Fukuyama coupling
 * Fukuyama indole synthesis
 * Gabriel synthesis
 * Gabriel-Colman rearrangement
 * Gassman indole synthesis
 * Gattermann reaction
 * Gattermann-Koch reaction
 * Gewald reaction
 * Goldberg reaction
 * Gomberg-Bachmann reaction
 * Gould-Jacobs reaction
 * Grieco elimination
 * Grignard reaction
 * Grob fragmentation
 * Guerbet reaction
 * Hajos-Parrish-Eder-Sauer-Wiechert reaction
 * Hammick reaction
 * Hantzsch pyridine synthesis
 * Hantzsch pyrrole synthesis
 * Hayashi rearrangement
 * Heck reaction
 * Hell-Volhard-Zelinsky halogenation
 * Hemetsberger indole synthesis
 * Herz reaction
 * Hiyama coupling
 * Hofmann elimination
 * Hofmann rearrangement
 * Hofmann-Löffler reaction
 * Hofmann-Martius rearrangement
 * Horner-Wadsworth-Emmons reaction
 * Hunsdiecker reaction
 * Hösch reaction
 * Ireland-Claisen rearrangement
 * Ivanov reaction
 * Jacobsen epoxidation
 * Jacobsen rearrangement
 * Japp-Klingemann reaction
 * Johnson-Corey-Chaykovsky reaction
 * Jones oxidation
 * Julia olefination
 * Kiliani-Fischer 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
 * Lehmstedt-Tanasescu reaction
 * Leimgruber-Batcho indole synthesis
 * Lemieux-Johnson oxidation
 * Letts nitrile synthesis
 * Leuckart reaction
 * Lobry-de Bruyn-van Ekenstein transformation
 * Lossen rearrangement
 * Luche reduction
 * Madelung synthesis
 * Mannich reaction
 * Martinet dioxindole synthesis
 * McFadyen-Stevens reaction
 * McLafferty rearrangement
 * McMurry reaction
 * Meerwein arylation
 * Meerwein-Ponndorf-Verley reduction
 * Menshutkin reaction
 * Meyer-Schuster rearrangement
 * Meyers synthesis
 * Michael reaction
 * Michaelis-Arbuzov reaction
 * Milas hydroxylation
 * Mitsunobu reaction
 * Mukaiyama aldol addition
 * Mumm rearrangement
 * Nazarov cyclization reaction
 * Neber rearrangement
 * Nef reaction
 * Negishi coupling
 * Nenitzescu indole synthesis
 * Nicholas reaction
 * Niementowski quinazoline synthesis
 * Niementowski quinoline synthesis
 * Nierenstein reaction
 * Norrish reaction
 * Noyori asymmetric hydrogenation
 * Nozaki-Hiyama-Kishi Nickel/Chromium Coupling reaction
 * Oppenauer oxidation
 * Overman rearrangement
 * Paal-Knorr synthesis
 * Passerini reaction
 * Paterno-Buchi reaction
 * Pauson–Khand reaction
 * Pechmann condensation
 * Pellizzari reaction
 * Perkin reaction
 * Perkow reaction
 * Petasis reaction
 * Peterson olefination
 * Pfitzinger reaction
 * Pfitzner-Moffatt oxidation
 * Pictet-Spengler reaction
 * Pinner reaction
 * Povarov reaction
 * Prato reaction
 * Prins reaction
 * Prévost reaction
 * Pummerer rearrangement
 * Ramberg-Bäcklund reaction
 * Rauhut-Currier reaction
 * Reed reaction
 * Reformatsky reaction
 * Reimer-Tiemann reaction
 * Reissert indole synthesis
 * Reissert reaction
 * Riemschneider thiocarbamate synthesis
 * Ritter reaction
 * Robinson annulation
 * Robinson-Gabriel synthesis
 * Rosenmund reduction
 * Rosenmund-von Braun synthesis
 * Rubottom oxidation
 * Rupe reaction
 * Ruzicka large ring synthesis
 * Sakurai reaction
 * Sandmeyer reaction
 * Sarett oxidation
 * Schiemann reaction
 * Schmidt reaction
 * Scholl reaction
 * 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
 * Sommelet reaction
 * Sonogashira coupling
 * Staudinger reaction
 * Stephen aldehyde synthesis
 * Stetter reaction
 * Stevens rearrangement
 * Stieglitz rearrangement
 * Stille reaction
 * Stollé synthesis
 * Stork enamine alkylation
 * Strecker amino acid synthesis
 * Suzuki reaction
 * Swern oxidation
 * Takai olefination
 * Thorpe reaction
 * Tiffeneau-Demjanov rearrangement
 * Tishchenko reaction
 * Trost asymmetric allylic alkylation
 * Ugi reaction
 * Ullmann condensation
 * Ullmann reaction
 * Upjohn dihydroxylation
 * Urech hydantoin synthesis
 * 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 rearrangement
 * Weerman degradation
 * 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 reaction
 * Wolff rearrangement
 * Wolff-Kishner reduction
 * Wolffenstein-Böters reaction
 * Woodward cis-hydroxylation
 * Wurtz reaction
 * Wurtz-Fittig reaction
 * Wöhler synthesis
 * Zincke reaction
 * Zincke-Suhl reaction
 * Zinke nitration
 * Étard reaction