User:Y-S.Ko/Wikipedia course/Chemistry

reactions

 * Alder ene reaction
 * Aldol condensation
 * Algar–Flynn–Oyamada reaction
 * Allan–Robinson reaction
 * Arndt–Eistert homologation
 * Baeyer–Villiger oxidation
 * Baker–Venkataraman rearrangement
 * Bamford–Stevens reaction
 * Baran reagents
 * Barbier reaction
 * Bargellini reaction
 * Bartoli indole synthesis
 * Barton radical decarboxylation
 * Barton–McCombie deoxygenation
 * Barton nitrite photolysis
 * Barton–Zard reaction
 * Batcho–Leimgruber indole synthesis
 * Baylis–Hillman reaction
 * Beckmann rearrangement
 * Abnormal Beckmann rearrangement
 * Beirut reaction
 * Benzilic acid rearrangement
 * Benzoin condensation
 * Bergman cyclization
 * Biginelli reaction
 * Birch reduction
 * Bischler–Möhlau indole synthesis
 * Bischler–Napieralski reaction
 * Blaise reaction
 * Blum–Ittah aziridine synthesis
 * Boekelheide reaction
 * Boger pyridine synthesis
 * Borch reductive amination
 * Borsche–Drechsel cyclization
 * Boulton–Katritzky rearrangement
 * Bouveault aldehyde synthesis
 * Bouveault–Blanc reduction
 * Boyland–Sims oxidation
 * Elbs oxidation
 * Bradsher reaction
 * Brook rearrangement
 * Brown hydroboration
 * Bucherer carbazole synthesis
 * Bucherer reaction
 * Bucherer–Bergs reaction
 * Büchner ring expansion
 * Buchwald–Hartwig amination
 * Burgess reagent
 * Burke boronates
 * Cadiot–Chodkiewicz coupling
 * Cadogan–Sundberg indole synthesis
 * Camps quinoline synthesis
 * Cannizzaro reaction
 * Carroll rearrangement
 * Castro–Stephens coupling
 * CíH activation
 * Catellani reaction
 * Sanford reaction
 * White catalyst
 * Yu CíH activation
 * Chan alkyne reduction
 * Chan–Lam C–X coupling reaction
 * Chapman rearrangement
 * Chichibabin pyridine synthesis
 * Ciamician–Dennsted rearrangement
 * Claisen condensation
 * Claisen isoxazole synthesis
 * Claisen rearrangements
 * para-Claisen rearrangement
 * Abnormal Claisen rearrangement
 * Chugaev elimination
 * Eschenmoser–Claisen amide acetal rearrangement
 * Ireland–Claisen (silyl ketene acetal) rearrangement
 * Johnson–Claisen (orthoester) rearrangement
 * Clemmensen reduction
 * Combes quinoline synthesis
 * Conrad–Limpach reaction
 * Cope elimination reaction
 * Cope rearrangement
 * Anionic oxy-Cope rearrangement
 * Oxy-Cope rearrangement
 * Siloxy-Cope rearrangement
 * Corey–Bakshi–Shibata (CBS) reagent
 * Corey Chaykovsky reaction
 * Corey–Fuchs reaction
 * Corey–Kim oxidation
 * Corey–Nicolaou macrolactonization
 * Corey–Seebach reaction
 * Corey–Winter olefin synthesis
 * Criegee glycol cleavage
 * Criegee mechanism of ozonolysis
 * Curtius rearrangement
 * Dakin oxidation
 * Dakin–West reaction
 * Danheiser annulation
 * Darzens condensation
 * Delépine amine synthesis
 * de Mayo reaction
 * Demjanov rearrangement
 * Tiffeneau–Demjanov rearrangement
 * Dess–Martin periodinane oxidation
 * Dieckmann condensation
 * Diels–Alder reaction
 * Inverse electronic demand Diels–Alder reaction
 * Hetero-Diels–Alder reaction
 * Dienone–phenol rearrangement
 * Doebner quinoline synthesis
 * Doebner–von Miller reaction
 * Dötz reaction
 * Dowd–Beckwith ring expansion
 * Dudley reagent
 * Erlenmeyer–Plöchl azlactone synthesis
 * Eschenmoser’s salt
 * Eschenmoser–Tanabe fragmentation
 * Eschweiler–Clarke reductive alkylation of amines
 * Evans aldol reaction
 * Favorskii rearrangement
 * Quasi-Favorskii rearrangement
 * Feist–Bénary furan synthesis
 * Ferrier carbocyclization
 * Ferrier glycal allylic rearrangement
 * Fiesselmann thiophene synthesis
 * Fischer–Speier esterification
 * Fischer indole synthesis
 * Fischer oxazole synthesis
 * Fleming–Kumada oxidation
 * Tamao–Kumada oxidation
 * Friedel–Crafts reaction
 * Friedel–Crafts acylation reaction
 * Friedel–Crafts alkylation reaction
 * Friedländer quinoline synthesis
 * Fries rearrangement
 * Fukuyama amine synthesis
 * Fukuyama reduction
 * Gabriel synthesis
 * Ing–Manske procedure
 * Gabriel–Colman rearrangement
 * Gassman indole synthesis
 * Gattermann–Koch reaction
 * Gewald aminothiophene synthesis
 * Glaser coupling
 * Eglinton coupling
 * Gomberg–Bachmann reaction
 * Gould–Jacobs reaction
 * Grignard reaction
 * Grob fragmentation
 * Guareschi–Thorpe condensation
 * Hajos–Wiechert reaction
 * Haller–Bauer reaction
 * Hantzsch dihydropyridine synthesis
 * Hantzsch pyrrole synthesis
 * Heck reaction
 * Heteroaryl Heck reaction
 * Hegedus indole synthesis
 * Hell–Volhard–Zelinsky reaction
 * Henry nitroaldol reaction
 * Hinsberg synthesis of thiophenes
 * Hiyama cross-coupling reaction
 * Hofmann elimination
 * Hofmann rearrangement
 * Hofmann–Löffler–Freytag reaction
 * Horner–Wadsworth–Emmons reaction
 * Houben–Hoesch reaction
 * Hunsdiecker–Borodin reaction
 * Jacobsen–Katsuki epoxidation
 * Japp–Klingemann hydrazone synthesis
 * Jones oxidation
 * Collins oxidation
 * PCC oxidation
 * PDC oxidation
 * Julia–Kocienski olefination
 * Julia–Lythgoe olefination
 * Kahne glycosidation
 * Knoevenagel condensation
 * Knorr pyrazole synthesis
 * Koch–Haaf carbonylation
 * Koenig–Knorr glycosidation
 * Kostanecki reaction
 * Kröhnke pyridine synthesis
 * Krapcho reaction
 * Kumada cross-coupling reaction
 * Lawesson’s reagent
 * Leuckart–Wallach reaction
 * Li A3 reaction
 * Lossen rearrangement
 * McFadyen–Stevens reduction
 * McMurry coupling
 * MacMillan catalyst
 * Mannich reaction
 * Markovnikov’s rule
 * Anti-Markovnikov
 * Martin’s sulfurane dehydrating reagent
 * Masamune–Roush conditions for the Horner–Emmons reaction
 * Meerwein’s salt
 * Meerwein–Ponndorf–Verley reduction
 * Meisenheimer complex
 * 1,2-Meisenheimer rearrangement
 * 2,3-Meisenheimer rearrangement
 * Meyers oxazoline method
 * Meyer–Schuster rearrangement
 * Michael addition
 * Michaelis–Arbuzov phosphonate synthesis
 * Midland reduction
 * Minisci reaction
 * Mislow–Evans rearrangement
 * Mitsunobu reaction
 * Miyaura borylation
 * Moffatt oxidation
 * Morgan–Walls reaction
 * Pictet–Hubert reaction
 * Mori–Ban indole synthesis
 * Mukaiyama aldol reaction
 * Mukaiyama Michael addition
 * Mukaiyama reagent
 * Myers–Saito cyclization
 * Nazarov cyclization
 * Neber rearrangement
 * Nef reaction
 * Negishi cross-coupling reaction
 * Nenitzescu indole synthesis
 * Newman–Kwart rearrangement
 * Nicholas reaction
 * Nicolaou IBX dehydrogenation
 * Noyori asymmetric hydrogenation
 * Nozaki–Hiyama–Kishi reaction
 * Nysted reagent
 * Oppenauer oxidation
 * Overman rearrangement
 * Paal thiophene synthesis
 * Paal–Knorr furan synthesis
 * Paal–Knorr pyrrole synthesis
 * Parham cyclization
 * Passerini reaction
 * Paternó–Büchi reaction
 * Pauson–Khand reaction
 * Payne rearrangement
 * Pechmann coumarin synthesis
 * Perkin reaction
 * Perkow vinyl phosphate synthesis
 * Petasis reaction
 * Petasis reagent
 * Peterson olefination
 * Pictet–Gams isoquinoline synthesis
 * Pictet–Spengler tetrahydroisoquinoline synthesis
 * Pinacol rearrangement
 * Pinner reaction
 * Polonovski reaction
 * Polonovski–Potier reaction
 * Pomeranz–Fritsch reaction
 * Schlittler–Müller modification
 * Pavorov reaction
 * Prévost trans-dihydroxylation
 * Prins reaction
 * Pschorr cyclization
 * Pummerer rearrangement
 * Ramberg–Bäcklund reaction
 * Reformatsky reaction
 * Regitz diazo synthesis
 * Reimer–Tiemann reaction
 * Reissert reaction
 * Reissert indole synthesis
 * Ring-closing metathesis (RCM)
 * Ritter reaction
 * Robinson annulation
 * Robinson–Gabriel synthesis
 * Robinson–Schöpf reaction
 * Rosenmund reduction
 * Rubottom oxidation
 * Rupe rearrangement
 * Saegusa oxidation
 * Sakurai allylation reaction
 * Sandmeyer reaction
 * Schiemann reaction
 * Schmidt rearrangement
 * Schmidt’s trichloroacetimidate glycosidation
 * Scholl reaction
 * Shapiro reaction
 * Sharpless asymmetric amino hydroxylation
 * Sharpless asymmetric dihydroxylation
 * Sharpless asymmetric epoxidation
 * Sharpless olefin synthesis
 * Shi asymmetric epoxidation
 * Simmons–Smith reaction
 * Skraup quinoline synthesis
 * Smiles rearrangement
 * Truce–Smile rearrangement
 * Sommelet reaction
 * Sommelet–Hauser rearrangement
 * Sonogashira reaction
 * Staudinger ketene cycloaddition
 * Staudinger reduction
 * Stetter reaction
 * Stevens rearrangement
 * Still–Gennari phosphonate reaction
 * Stille coupling
 * Stille–Kelly reaction
 * Stobbe condensation
 * Stork–Danheiser transposition
 * Strecker amino acid synthesis
 * Suzuki–Miyaura coupling
 * Swern oxidation
 * Takai reaction
 * Tebbe reagent
 * TEMPO oxidation
 * Thorpe Ziegler reaction
 * Tsuji–Trost reaction
 * Ugi reaction
 * Ullmann coupling
 * van Leusen oxazole synthesis
 * Vilsmeier–Haack reaction
 * Vinylcyclopropane cyclopentene rearrangement
 * von Braun reaction
 * Wacker oxidation
 * Wagner–Meerwein rearrangement
 * Weiss–Cook condensation
 * Wharton reaction
 * Williamson ether synthesis
 * Willgerodt–Kindler reaction
 * Wittig reaction
 * Schlosser modification of the Wittig reaction
 * 1,2-Wittig rearrangement
 * 2,3-Wittig rearrangement
 * Wohl–Ziegler reaction
 * Wolff rearrangement
 * Wolff–Kishner reduction
 * Woodward cis-dihydroxylation
 * Yamaguchi esterification
 * Zaitsev’s elimination rule
 * Zhang enyne cycloisomerization
 * Zimmerman rearrangement
 * Zincke reaction
 * Zinin benzidine (semidne) rearrangement
 * Zinin benzidine (semidne) rearrangement