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

Chemistry

reactions

Chemical reactions

Functional group	Preparation	Reactions
Acid anhydride	preparation	reactions
Acyl halides	preparation	reactions
Acyloins	preparation	reactions
Alcohols	preparation	reactions
Aldehydes	preparation	reactions
Alkanes	preparation	reactions
Alkenes	preparation	reactions
Alkyl halides	preparation	reactions
Alkyl nitrites	preparation	reactions
Alkynes	preparation	reactions
Amides	preparation	reactions
Amine oxide	preparation	reactions
Amines	preparation	reactions
Arene compounds	preparation	reactions
Azides	preparation	reactions
Aziridines	preparation	reactions
Carboxylic acids	preparation	reactions
Cyclopropanes	preparation	reactions
Diazo compounds	preparation	reactions
Diols	preparation	reactions
Esters	preparation	reactions
Ethers	preparation	reactions
Epoxide	preparation	reactions
Haloketones	preparation	reactions
Imines	preparation	reactions
Isocyanates	preparation	reactions
Ketones	preparation	reactions
Lactams	preparation	reactions
Lactones	preparation	reactions
Nitriles	preparation	reactions
Nitro compounds	preparation	reactions
Phenols	preparation	reactions
Thiols	preparation	reactions

• Name 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

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