List of organic reactions

• 1,2-Wittig rearrangement • 1,3-Dipolar cycloaddition • 2,3-Wittig rearrangement ==A==

• Acetalisation • Acetoacetic ester condensation • Achmatowicz reaction • Acylation • Acyloin condensation • Adams' catalyst • Adams decarboxylation • Adkins catalyst • Adkins–Peterson reaction • Akabori amino acid reaction • Alcohol oxidation • Alder ene reaction • Alder–Stein rules • Aldol addition • Aldol condensation • Algar–Flynn–Oyamada reaction • Alkylimino-de-oxo-bisubstitution • Alkyne trimerisation • Alkyne zipper reaction • Allan–Robinson reaction • Allylic rearrangement • Amadori rearrangement • Amine alkylation • Angeli–Rimini reaction • Andrussov oxidation • Appel reaction • Arbuzov reaction, Arbusow reaction • Arens–Van Dorp synthesis, Isler modification • Aromatic nitration • Arndt–Eistert synthesis • Aston–Greenburg rearrangement • Auwers synthesis • Aza-Cope rearrangement • Azo coupling ==B==

• Baeyer–Drewson indigo synthesis • Baeyer–Villiger oxidation, Baeyer–Villiger rearrangement • Bakeland process (Bakelite) • Baker–Venkataraman rearrangement, Baker–Venkataraman transformation • Baldwin's rules • Bally–Scholl synthesis • Balz–Schiemann reaction • Bamberger rearrangement • Bamberger triazine synthesis • Bamford–Stevens reaction • Barbier reaction • Barbier–Wieland degradation • Bardhan–Sengupta phenanthrene synthesis • Barfoed's test • Bargellini reaction • Bartoli indole synthesis, Bartoli reaction • Barton decarboxylation • Barton reaction • Barton–Kellogg reaction • Barton–McCombie reaction, Barton deoxygenation • Barton-Zard Synthesis • Barton vinyl iodine procedure • Baudisch reaction • Bayer test • Baylis–Hillman reaction • Bechamp reaction • Bechamp reduction • Beckmann fragmentation • Beckmann rearrangement • Bellus–Claisen rearrangement • Belousov–Zhabotinsky reaction • Benary reaction • Benedict's reagent • Benkeser reaction • Benzidine rearrangement • Benzilic acid rearrangement • Benzoin condensation • Bergman cyclization • Bergmann azlactone peptide synthesis • Bergmann degradation • Bergmann–Zervas carbobenzoxy method • Bernthsen acridine synthesis • Bestmann's reagent • Betti reaction • Biginelli pyrimidine synthesis • Biginelli reaction • Bingel reaction • Birch reduction • Bischler–Möhlau indole synthesis • Bischler–Napieralski reaction • Biuret test • Blaise ketone synthesis • Blaise reaction • Blanc reaction • Blanc chloromethylation • Blum–Ittah aziridine synthesis • Bodroux reaction • Bodroux–Chichibabin aldehyde synthesis • Bogert–Cook synthesis • Bohlmann-Rahtz pyridine synthesis • Bohn–Schmidt reaction • Boord olefin synthesis • Borodin reaction • Borsche–Drechsel cyclization • Bosch–Meiser urea process • Bosch reaction • Bouveault aldehyde synthesis • Bouveault–Blanc reduction • Boyland–Sims oxidation • Boyer Reaction • Bredt's rule • Brook rearrangement • Brown hydroboration • Bucherer carbazole synthesis • Bucherer reaction • Bucherer–Bergs reaction • Buchner ring enlargement • Büchner–Curtius–Schlotterbeck reaction • Buchwald–Hartwig amination • Bunnett reaction • Burgess reagent ==C==

• Cadiot–Chodkiewicz coupling • Cadogan-Sundberg indole synthesis • Camps quinoline synthesis • Cannizzaro reaction • Carbohydrate acetalisation • Carbonyl reduction • Carbonylation • Carbylamine reaction • Carroll reaction • Castro–Stephens coupling • Catalytic reforming • Catellani Reaction • CBS reduction • Chan–Lam coupling • Chapman rearrangement • Cheletropic reaction • Chichibabin pyridine synthesis • Chichibabin reaction • Chiral pool synthesis • Chugaev elimination • Ciamician–Dennstedt rearrangement • Claisen condensation • Claisen rearrangement • Claisen–Schmidt condensation • Clemmensen reduction • Collins reagent • Combes quinoline synthesis • Conia reaction • Conrad–Limpach synthesis • Cook–Heilbron thiazole synthesis • Cope elimination • Cope rearrangement • Corey reagent • Corey–Bakshi–Shibata reduction • Corey–Fuchs reaction • Corey–Gilman–Ganem oxidation • Corey–Kim oxidation • Corey-Nicolaou macrolactonization • Corey–Posner, Whitesides–House reaction • Corey-Seebach reaction • Corey–Winter olefin synthesis • Corey–Winter reaction • Cornforth rearrangement • Coupling reaction • Crabbé reaction • Craig method • Cram's rule of asymmetric induction • Creighton process • Criegee reaction • Criegee rearrangement • Cross metathesis • Crum Brown–Gibson rule • Curtius degradation • Curtius rearrangement, Curtius reaction • Cyanohydrin reaction ==D==

• Dakin reaction (aka Dakin oxidation) • Dakin–West reaction • Danheiser annulation • Danheiser benzannulation • Darapsky degradation • Darzens condensation, Darzens–Claisen reaction, Glycidic ester condensation • Darzens halogenation • Darzens synthesis of unsaturated ketones • Darzens tetralin synthesis • Davis' reagent, Davis oxidation • Davis–Beirut reaction • De Kimpe aziridine synthesis • Dehydration reaction • Dehydrogenation • Delépine reaction • DeMayo reaction • Demjanov rearrangement • Demjanow desamination • Dess–Martin oxidation • Diazoalkane 1,3-dipolar cycloaddition • Diazotisation • DIBAL-H selective reduction • Dieckmann condensation • Dieckmann reaction • Diels–Alder reaction • Diels–Reese reaction • Dienol–benzene rearrangement • Dienone–phenol rearrangement • Dimroth rearrangement • Di-π-methane rearrangement • Directed ortho metalation • Doebner modification • Doebner reaction • Doebner–Miller reaction, Beyer method for quinolines • Doering–LaFlamme carbon chain extension • Dötz reaction • Dowd–Beckwith ring expansion reaction • Duff reaction • Dutt–Wormall reaction • Dyotropic reaction ==E==

• E1cB elimination reaction • Eder reaction • Edman degradation • Eglinton reaction • Ehrlich–Sachs reaction • Einhorn variant • Einhorn–Brunner reaction • Elbs persulfate oxidation • Elbs reaction • Electrochemical fluorination • Electrocyclic reaction • Electrophilic halogenation • Electrophilic amination • Elimination reaction • Emde degradation • Emmert reaction • Enders SAMP/RAMP hydrazone-alkylation reaction • Ene reaction • Enyne metathesis • Epoxidation • Erlenmeyer synthesis, Azlactone synthesis • Erlenmeyer–Plöchl azlactone and amino-acid synthesis • Eschenmoser fragmentation • Eschenmoser sulfide contraction • Eschweiler–Clarke reaction • Ester pyrolysis • Ether cleavage • Étard reaction • Evans aldol • Evans–Saksena reduction • Evans–Tishchenko reaction ==F==

• Favorskii reaction • Favorskii rearrangement • Favorskii–Babayan synthesis • Fehling test • Feist–Benary synthesis • Fenton reaction • Ferrario reaction • Ferrier carbocyclization • Ferrier rearrangement • Fétizon oxidation • Fiesselmann thiophene synthesis • Finkelstein reaction • Fischer indole synthesis • Fischer oxazole synthesis • Fischer peptide synthesis • Fischer phenylhydrazine and oxazone reaction • Fischer glycosidation • Fischer–Hepp rearrangement • Fischer–Speier esterification • Fischer Tropsch synthesis • Fleming–Tamao oxidation • Flood reaction • Folin–Ciocalteu reagent • Formox process • Forster reaction • Forster–Decker method • Fowler process • Franchimont reaction • Frankland synthesis • Frankland–Duppa reaction • Fráter–Seebach alkylation • Free radical halogenation • Freund reaction • Friedel–Crafts acylation • Friedel–Crafts alkylation • Friedländer synthesis • Fries rearrangement • Fritsch–Buttenberg–Wiechell rearrangement • Fujimoto–Belleau reaction • Fujiwara–Moritani reaction • Fukuyama coupling • Fukuyama indole synthesis • Fukuyama reduction ==G==

• Gabriel ethylenimine method • Gabriel synthesis • Gabriel–Colman rearrangement, Gabriel isoquinoline synthesis • Gallagher–Hollander degradation • Gassman indole synthesis • Gastaldi synthesis • Gattermann aldehyde synthesis • Gattermann Koch reaction • Gattermann reaction • Geminal halide hydrolysis • Gewald reaction • Gibbs phthalic anhydride process • Gilman reagent • Glaser coupling • Glycol cleavage • Goldberg reaction • Gomberg–Bachmann reaction • Gomberg–Bachmann–Hey reaction • Gomberg radical reaction • Gould–Jacobs reaction • Graebe–Ullmann synthesis • Grignard degradation • Griesbaum coozonolysis • Grignard reaction • Grob fragmentation • Grubbs' catalyst in Olefin metathesis • Grundmann aldehyde synthesis • Gryszkiewicz–Trochimowski and McCombie method • Guareschi–Thorpe condensation • Guerbet reaction • Gutknecht pyrazine synthesis ==H==

• Hajos–Parrish–Eder–Sauer–Wiechert reaction • Haller–Bauer reaction • Haloform reaction • Halogen addition reaction • Halohydrin formation reaction • Hammick reaction • Hammond principle or Hammond postulate • Hantzsch pyrrole synthesis • Hantzsch dihydropyridine synthesis, Hantzsch pyridine synthesis • Hantzsch pyridine synthesis, Gattermann–Skita synthesis, Guareschi–Thorpe condensation, Knoevenagel–Fries modification • Hantzsch–Collidin synthesis • Harries ozonolysis • Haworth methylation • Haworth synthesis • Hay coupling • Hayashi rearrangement • Heck reaction • Hegedus indole synthesis • Helferich method • Hell–Volhard–Zelinsky halogenation • Hemetsberger indole synthesis • Hemetsberger–Knittel synthesis • Henkel reaction, Raecke process, Henkel process • Henry reaction, Kamlet reaction • Herz reaction, Herz compounds • Herzig–Meyer alkimide group determination • Heumann indigo synthesis • Hiyama coupling • Hydration reaction • Hydroamination • Hydrodesulfurization • Hydrogenolysis • Hydrosilylation • Hinsberg indole synthesis • Hinsberg oxindole synthesis • Hinsberg reaction • Hinsberg separation • Hinsberg sulfone synthesis • Hirao coupling • Hoch–Campbell ethylenimine synthesis • Hock rearrangement • Hofmann bromamide reaction • Hofmann degradation, Exhaustive methylation • Hofmann elimination • Hofmann Isonitrile synthesis, Carbylamine reaction • Hofmann product • Hofmann rearrangement • Hofmann–Löffler reaction, Löffler–Freytag reaction, Hofmann–Löffler–Freytag reaction • Hofmann–Martius rearrangement • Hofmann's rule • Hofmann–Sand reaction • Homo rearrangement of steroids • Hooker reaction • Horner–Wadsworth–Emmons reaction • Hoesch reaction • Hosomi–Sakurai reaction • Houben–Fischer synthesis • Hudlicky fluorination • Huisgen cycloaddition • Hunsdiecker reaction, Hunsdiecker–Borodin reaction • Hurd-Mori 1,2,3-thiadiazole synthesis • Hurtley reaction • Hydroboration • Hydrocarbon cracking • Hydrohalogenation ==I==

• Indium mediated allylation • Ing–Manske procedure • Ipso substitution • Ireland–Claisen rearrangement • Isay reaction • Ishikawa reagent • trans-cis isomerism • Ivanov reagent, Ivanov reaction ==J==

• Jacobsen epoxidation • Jacobsen rearrangement • Janovsky reaction • Japp–Klingemann reaction • Japp–Maitland condensation • Jocic reaction • Johnson–Claisen rearrangement • Johnson–Corey–Chaykovsky reaction • Jones oxidation • Jordan–Ullmann–Goldberg synthesis • Julia olefination, Julia–Lythgoe olefination ==K==

• Kabachnik–Fields reaction • Kharasch–Sosnovsky reaction • Keck asymmetric allylation • Ketimine Mannich reaction • Ketone halogenation • Kiliani–Fischer synthesis • Kindler reaction • Kishner cyclopropane synthesis • Knoevenagel condensation • Knorr pyrazole synthesis • Knorr pyrrole synthesis • Knorr quinoline synthesis • Koch–Haaf reaction • Kochi reaction • Koenigs–Knorr reaction • Kolbe electrolysis • Kolbe nitrile synthesis • Kolbe–Schmitt reaction • Kornblum oxidation • Kornblum–DeLaMare rearrangement • Kostanecki acylation • Kowalski ester homologation • Krapcho decarboxylation • Krische allylation • Kröhnke aldehyde synthesis • Kröhnke oxidation • Kröhnke pyridine synthesis • Kucherov reaction • Kuhn–Winterstein reaction • Kulinkovich reaction • Kumada coupling ==L==

• Larock indole synthesis • Lawesson's reagent • Lebedev process • Lehmstedt–Tanasescu reaction • Leimgruber–Batcho indole synthesis • Letts nitrile synthesis • Leuckart reaction • Leuckart thiophenol reaction • Leuckart–Wallach reaction • Leuckart amide synthesis • Levinstein process • Ley oxidation • Lieben iodoform reaction, Haloform reaction • Liebeskind–Srogl coupling • Liebig melamine synthesis • Lindlar catalyst • Lobry de Bruyn–Van Ekenstein transformation • Lombardo methylenation • Lossen rearrangement • Lucas' reagent • Luche reduction ==M==

• Maillard reaction • Madelung synthesis • Malaprade reaction, Periodic acid oxidation • Malonic ester synthesis • Mannich reaction • Markó–Lam deoxygenation • Markovnikov's rule, Markownikoff rule, Markownikow rule • Marschalk reaction • Martinet dioxindole synthesis • McDougall monoprotection • McFadyen–Stevens reaction • McMurry reaction • Meerwein arylation • Meerwein–Ponndorf–Verley reduction • Meisenheimer rearrangement • Meissenheimer complex • Menshutkin reaction • Metal-ion-catalyzed σ-bond rearrangement • Mesylation • Merckwald asymmetric synthesis • Metallo-ene reaction • Methylation • Meyer and Hartmann reaction • Meyer reaction • Meyer synthesis • Meyer–Schuster rearrangement • Michael addition • Michael addition, Michael system • Michael condensation • Michaelis–Arbuzov reaction • Midland Alpine borane reduction • Mignonac reaction • Milas hydroxylation of olefins • Minisci reaction • Mislow–Evans rearrangement • Mitsunobu reaction • Miyaura borylation • Modified Wittig-Claisen tandem reaction • Molisch's test • Mozingo reduction • Mukaiyama aldol addition (Mukaiyama reaction) • Mukaiyama hydration • Myers' asymmetric alkylation ==N==

• Nametkin rearrangement • Narasaka–Prasad reduction • Nazarov cyclization reaction • Neber rearrangement • Nef reaction • Negishi coupling • Negishi zipper reaction • Nenitzescu indole synthesis • Nenitzescu reductive acylation • Newman–Kwart rearrangement • Nicholas reaction • Niementowski quinazoline synthesis • Niementowski quinoline synthesis • Nierenstein reaction • NIH shift • Ninhydrin test • Nitroaldol reaction • Nitrone-olefin 3+2 cycloaddition • Normant reagents • Noyori asymmetric hydrogenation • Nozaki–Hiyama–Kishi reaction • Nucleophilic acyl substitution ==O==

• Ohira–Bestmann reaction • Olah reagent • Olefin metathesis • Oppenauer oxidation • Orton rearrangement • Ostromyslenskii reaction, Ostromisslenskii reaction • Overman rearrangement • Oxidative decarboxylation • Oxo synthesis • Oxy-Cope rearrangement • Oxymercuration • Oxidation of alcohols to carbonyl compounds • Ozonolysis ==P==

• Paal–Knorr pyrrole synthesis • Paal–Knorr synthesis • Paneth technique • Passerini reaction • Paternò–Büchi reaction • Pauson–Khand reaction • Payne rearrangement • Pechmann condensation • Pechmann pyrazole synthesis • Pellizzari reaction • Pelouze synthesis • Peptide synthesis • Perkin alicyclic synthesis • Perkin reaction • Perkin rearrangement • Perkow reaction • Petasis reaction • Petasis reagent • Peterson olefination • Peterson reaction • Petrenko-Kritschenko piperidone synthesis • Pfau–Plattner azulene synthesis • Pfitzinger reaction • Pfitzner–Moffatt oxidation • Phosphonium coupling • Photosynthesis • Piancatelli rearrangement • Pictet–Gams isoquinoline synthesis • Pictet–Hubert reaction • Pictet–Spengler tetrahydroisoquinoline synthesis • Pictet–Spengler reaction • Piloty–Robinson pyrrole synthesis • Pinacol coupling reaction • Pinacol rearrangement • Pinner amidine synthesis • Pinner method for ortho esters • Pinner reaction • Pinner triazine synthesis • Pinnick oxidation • Piria reaction • Polonovski reaction • Pomeranz–Fritsch reaction • Ponzio reaction • Prato reaction • Prelog strain • Prevost reaction • Prileschajew reaction • Prilezhaev reaction • Prins reaction • Prinzbach synthesis • Protecting group • Pschorr reaction • Pummerer rearrangement • Purdie methylation, Irvine–Purdie methylation • PUREX ==Q==

• Ramberg–Bäcklund reaction • Raney nickel • Rap–Stoermer condensation • Raschig phenol process • Rauhut–Currier reaction • Racemization • Reductive amination • Reductive dehalogenation of halo ketones • Reed reaction • Reformatskii reaction, Reformatsky reaction • Reilly–Hickinbottom rearrangement • Reimer–Tiemann reaction • Reissert indole synthesis • Reissert reaction, Reissert compound • Reppe synthesis • Retropinacol rearrangement • Rieche formylation • Riemschneider thiocarbamate synthesis • Riley oxidations • Ring closing metathesis • Ring opening metathesis • Ritter reaction • Robinson annulation • Robinson–Gabriel synthesis • Robinson Schopf reaction • Rosenmund reaction • Rosenmund reduction • Rosenmund–von Braun synthesis • Roskamp reaction • Rothemund reaction • Rupe rearrangement • Rubottom oxidation • Ruff–Fenton degradation • Ruzicka large-ring synthesis ==S==

• Saegusa–Ito oxidation • Sakurai reaction • Salol reaction • Sandheimer • Sandmeyer diphenylurea isatin synthesis • Sandmeyer isonitrosoacetanilide isatin synthesis • Sandmeyer reaction • Sanger reagent • Saponification • Sarett oxidation • Schiemann reaction • Sharpless oxyamination or aminohydroxylation • Shenck ene reaction • Shi epoxidation • Shiina esterification • Shiina macrolactonization or Shiina lactonization • Sigmatropic reaction • Simmons–Smith reaction • Simonini reaction • Simonis chromone cyclization • Simons process • Skraup chinolin synthesis • Skraup reaction • Smiles rearrangement • SNAr nucleophilic aromatic substitution • SN1 • SN2 • SNi • Solvolysis • Sommelet reaction • Sonn–Müller method • Sonogashira coupling • Sørensen formol titration • Staedel–Rugheimer pyrazine synthesis • Stahl oxidation • Staudinger reaction • Staudinger synthesis • Steglich esterification • Stephen aldehyde synthesis • Stephens-Castro coupling • Stetter reaction • Stevens rearrangement • Stieglitz rearrangement • Stille coupling • Stobbe condensation • Stollé synthesis • Stork acylation • Stork enamine alkylation • Strecker amino acid synthesis • Strecker degradation • Strecker sulfite alkylation • Strecker synthesis • Stereocontrolled 1,2-addition to carbonyl groups • Suzuki coupling • Swain equation • Swarts reaction • Swern oxidation ==T==

• Tamao oxidation • Tafel rearrangement • Takai olefination • Tebbe olefination • ter Meer reaction • Thiele reaction • Thiol-yne reaction • Thorpe reaction • Tiemann rearrangement • Tiffeneau ring enlargement reaction • Tiffeneau–Demjanov rearrangement • Tischtschenko reaction • Tishchenko reaction, Tishchenko–Claisen reaction • Tollens' reagent • Transfer hydrogenation • Trapp mixture • Transesterification • Traube purine synthesis • Truce–Smiles rearrangement • Tscherniac–Einhorn reaction • Tschitschibabin reaction • Tschugajeff reaction • Tsuji–Trost reaction • Tsuji–Wilkinson decarbonylation reaction • Twitchell process • Tyrer sulfonation process ==U==