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~Organic Chemistry~

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1,3-Butadiene
1,3-Dipolar cycloaddition
1-Fluoro-2,4-dinitrobenzene
2,3-Wittig rearrangement
2-Pyridone
Acetal
Acetylene
Acetylide
Achmatowicz reaction
Acylation
Acyloin condensation
Adams decarboxylation
Adams's catalyst
Adkins–Peterson reaction
Akabori amino-acid reaction
Alcohol oxidation
Aldehyde
Aldol condensation
Aldol reaction
Algar–Flynn–Oyamada reaction
Alkylimino-de-oxo-bisubstitution
Alkyne trimerisation
Alkyne zipper reaction
Allan–Robinson reaction
Allylic rearrangement
Amadori rearrangement
Amide
Amine alkylation
Amine oxide
Andrussow process
Angeli–Rimini reaction
Anthraquinone
Antimony trifluoride
Appel reaction
Arene substitution pattern
Arndt–Eistert reaction
Aromatic sulfonation
Asymmetric induction
Auwers synthesis
Azide
Aziridine
Azo coupling
Azulene
Baeyer's reagent
Baeyer–Drewson indigo synthesis
Baeyer–Villiger oxidation
Baker–Venkataraman rearrangement
Balz–Schiemann reaction
Bamberger rearrangement
Bamberger triazine synthesis
Bamford–Stevens reaction
Barfoed's test
Bargellini reaction
Bartoli indole synthesis
Barton reaction
Barton–Kellogg reaction
Barton–McCombie deoxygenation
Barton–Zard reaction
Baudisch reaction
Baylis–Hillman reaction
Bechamp reaction
Bechamp reduction
Beckmann rearrangement
Belousov–Zhabotinsky reaction
Benary reaction
Benedict's reagent
Benkeser reaction
Benzidine
Benzilic acid rearrangement
Benzofuran
Benzoin condensation
Bergman cyclization
Bergmann azlactone peptide synthesis
Bergmann degradation
Bernthsen acridine synthesis
Betti reaction
Biginelli reaction
Bingel reaction
Birch reduction
Bischler–Möhlau indole synthesis
Bischler–Napieralski reaction
Biuret test
Blaise ketone synthesis
Blaise reaction
Blanc chloromethylation
Bodroux–Chichibabin aldehyde synthesis
Boord olefin synthesis
Boronic acid
Bosch reaction
Bouveault aldehyde synthesis
Bouveault–Blanc reduction
Boyland–Sims oxidation
Bredt's rule
Bucherer carbazole synthesis
Bucherer reaction
Bucherer–Bergs reaction
Buchner ring expansion
Buchwald–Hartwig amination
Büchner–Curtius–Schlotterbeck reaction
Cadiot–Chodkiewicz coupling
Camps quinoline synthesis
Cannizzaro reaction
Carbazole
Carbohydrate acetalisation
Carbon monoxide
Carbonyl reduction
Carbonylation
Carboxybenzyl
Carboxylic acid
Carbylamine reaction
Carroll rearrangement
Cascade reaction
Castro–Stephens coupling
Catalytic reforming
Catellani reaction
CBS catalyst
Cheletropic reaction
Chichibabin pyridine synthesis
Chichibabin reaction
Chiral auxiliary
Chiral pool synthesis
Chugaev elimination
Claisen condensation
Claisen rearrangement
Clemmensen reduction
Collins reagent
Combes quinoline synthesis
Conrad–Limpach synthesis
Cook–Heilbron thiazole synthesis
Cope reaction
Cope rearrangement
Copper chromite
Corey–Fuchs reaction
Corey–House synthesis
Corey–Itsuno reduction
Corey–Kim oxidation
Corey–Winter olefin synthesis
Coupling reaction
Cracking (chemistry)
Creighton process
Criegee rearrangement
Cumene process
Curtius rearrangement
Cyanohydrin reaction
Cyclooctadecanonaene
Cyclopropanation
Cyclopropane
Dakin–West reaction
Danheiser annulation
Danheiser benzannulation
Darzens halogenation
Darzens reaction
Dehydration reaction
Dehydrogenation
Delépine reaction
Demjanov rearrangement
Dess–Martin oxidation
Dess–Martin periodinane
Di-pi-methane rearrangement
Diazoalkane 1,3-dipolar cycloaddition
Diazonium compound
Dieckmann condensation
Diels–Alder reaction
Diels–Reese reaction
Diisobutylaluminium hydride
Dimethyl sulfate
Dimroth rearrangement
Diphosphorus tetraiodide
Directed ortho metalation
Doebner reaction
Doebner–Miller reaction
Doering–LaFlamme allene synthesis
Dowd–Beckwith ring-expansion reaction
Duff reaction
Dyotropic reaction
E1cB-elimination reaction
Edman degradation
Einhorn–Brunner reaction
Elbs persulfate oxidation
Elbs reaction
Electrochemical fluorination
Electrocyclic reaction
Electrophilic amination
Electrophilic aromatic directing groups
Electrophilic halogenation
Electrosynthesis
Elimination reaction
Emde degradation
Enantioselective synthesis
Ene reaction
Enyne metathesis
Epoxide
Erlenmeyer–Plöchl azlactone and amino-acid synthesis
Eschenmoser fragmentation
Eschweiler–Clarke reaction
Ester pyrolysis
Ether
Favorskii reaction
Favorskii rearrangement
Fehling's solution
Feist–Benary synthesis
Fenton's reagent
Ferrier carbocyclization
Ferrier rearrangement
Finkelstein reaction
Fischer glycosidation
Fischer indole synthesis
Fischer oxazole synthesis
Fischer–Hepp rearrangement
Fischer–Speier esterification
Fischer–Tropsch process
Fleming–Tamao oxidation
Fluorination with aminosulfuranes
Fluorocarbon
Folin–Ciocalteu reagent
Formox process
Forster–Decker method
Free-radical halogenation
Free-radical reaction
Friedel–Crafts reaction
Friedländer synthesis
Fries rearrangement
Fritsch–Buttenberg–Wiechell rearrangement
Fujimoto–Belleau reaction
Fukuyama coupling
Fukuyama indole synthesis
Fukuyama reduction
Gabriel synthesis
Gabriel–Colman rearrangement
Gallagher–Hollander degradation
Gassman indole synthesis
Gattermann reaction
Geminal halide hydrolysis
Gewald reaction
Gilman reagent
Glaser coupling
Glycol cleavage
Gomberg–Bachmann reaction
Gould–Jacobs reaction
Grignard reaction
Grob fragmentation
Grubbs' catalyst
Grundmann aldehyde synthesis
Guerbet reaction
Haber–Weiss reaction
Haloform reaction
Halogen addition reaction
Halohydrin
Hammett equation
Hammick reaction
Hammond's postulate
Hantzsch pyridine synthesis
Hantzsch pyrrole synthesis
Hayashi rearrangement
Heck reaction
Helferich method
Hell–Volhard–Zelinsky halogenation
Hemetsberger indole synthesis
Herz reaction
Hinsberg oxindole synthesis
Hinsberg reaction
Hoesch reaction
Hofmann elimination
Hofmann rearrangement
Hofmann–Löffler reaction
Hofmann–Martius rearrangement
Hooker reaction
Horner–Wadsworth–Emmons reaction
Hunsdiecker reaction
Hydration reaction
Hydrazone iodination
Hydroamination
Hydroboration
Hydroboration–oxidation reaction
Hydrodesulfurization
Hydroformylation
Hydrogenolysis
Hydrohalogenation
Hydrosilylation
Indigo dye
Indium-mediated allylation
Isatin
Ishikawa reagent
Isocyanide
Isomer
Ivanov reaction
Jacobsen epoxidation
Jacobsen rearrangement
Japp–Klingemann reaction
Japp–Maitland condensation
Jones oxidation
Julia olefination
Kabachnik–Fields reaction
Ketene
Ketone
Ketone halogenation
Kharasch–Sosnovsky reaction
Kiliani–Fischer synthesis
Knoevenagel condensation
Knorr pyrrole synthesis
Knorr quinoline synthesis
Kochi reaction
Koenigs–Knorr reaction
Kolbe electrolysis
Kolbe–Schmitt reaction
Kornblum oxidation
Kornblum–DeLaMare rearrangement
Kostanecki acylation
Kowalski ester homologation
Krapcho decarboxylation
Kröhnke pyridine synthesis
Kulinkovich reaction
Kumada coupling
Larock indole synthesis
Lehmstedt–Tanasescu reaction
Leimgruber–Batcho indole synthesis
Letts nitrile synthesis
Leuckart reaction
Leuckart thiophenol reaction
Liebeskind–Srogl coupling
Lindlar catalyst
List of organic reactions
Lobry de Bruyn–van Ekenstein transformation
Lossen rearrangement
Lucas' reagent
Luche reduction
Madelung synthesis
Maillard reaction
Malaprade reaction
Malonic ester synthesis
Mannich reaction
Markovnikov's rule
Markó–Lam deoxygenation
Martinet dioxindole synthesis
McFadyen–Stevens reaction
McMurry reaction
Meerwein arylation
Meerwein–Ponndorf–Verley reduction
Meisenheimer complex
Melamine
Menshutkin reaction
Mercury(I) chloride
Mesylate
Methylation
Meyer–Schuster rearrangement
Michael reaction
Michaelis–Arbuzov reaction
Milas hydroxylation
Minisci reaction
Mitsunobu reaction
Molisch's test
Mukaiyama aldol addition
Nazarov cyclization reaction
Neber rearrangement
Nef reaction
Negishi coupling
Nenitzescu indole synthesis
Nicholas reaction
Niementowski quinazoline synthesis
Niementowski quinoline synthesis
Nierenstein reaction
NIH shift
Ninhydrin
Nitration
Nitrile
Nitrite
Nitro compound
Nitroaldol reaction
Nitrone-olefin (3+2) cycloaddition
Nitrosobenzene
Noyori asymmetric hydrogenation
Nozaki–Hiyama–Kishi reaction
Nucleophilic acyl substitution
Nucleophilic aromatic substitution
Olah reagent
Olefin metathesis
Oppenauer oxidation
Organocopper compound
Organomercury
Organoselenium chemistry
Organosilicon
Organosodium chemistry
Organosulfur compounds
Organozinc compound
Osazone
Oxidation of secondary alcohols to ketones
Oxime
Oxy-Cope rearrangement
Oxymercuration reaction
Ozonolysis
Paal–Knorr synthesis
Pagodane
Passerini reaction
Paternò–Büchi reaction
Pauson–Khand reaction
Payne rearrangement
Pechmann condensation
Pellizzari reaction
Peptide synthesis
Periodinane
Perkin reaction
Perkow reaction
Petasis reagent
Peterson olefination
Petrenko-Kritschenko piperidone synthesis
Pfitzinger reaction
Pfitzner–Moffatt oxidation
Phenanthrene
Phenanthridine
Phenol formaldehyde resin
Phenols
Phenyl salicylate
Photosynthesis
Phthalic anhydride
Piancatelli rearrangement
Pictet–Spengler reaction
Pinacol coupling reaction
Pinacol rearrangement
Pinner reaction
Pinner triazine synthesis
Pinnick oxidation
Pomeranz–Fritsch reaction
Porphyrin
Prato reaction
Prelog strain
Prilezhaev reaction
Prins reaction
Protecting group
Prévost reaction
Pummerer rearrangement
Pyrazine
Pyrazole
Pyridine
Pyrrole
Pyruvate dehydrogenase
Quelet reaction
Racemization
Radical-nucleophilic aromatic substitution
Ramberg–Bäcklund reaction
Raney nickel
Raschig–Hooker process
Rauhut–Currier reaction
Reductive amination
Reductive dehalogenation of halo ketones
Reed reaction
Reformatsky reaction
Reimer–Tiemann reaction
Reissert indole synthesis
Reissert reaction
Rieche formylation
Riemschneider thiocarbamate synthesis
Ritter reaction
Robinson annulation
Robinson–Gabriel synthesis
Rosenmund reduction
Rosenmund–von Braun reaction
Rubottom oxidation
Ruzicka large-ring synthesis
Sakurai reaction
Salicylaldehyde
Salt metathesis reaction
Sandmeyer reaction
Saponification
Sarett oxidation
Schiff base
Schiff test
Schlenk equilibrium
Schmidt reaction
Scholl reaction
Schotten–Baumann reaction
Seliwanoff's test
Seyferth–Gilbert homologation
Shapiro reaction
Sharpless asymmetric dihydroxylation
Sharpless epoxidation
Sharpless oxyamination
Sigmatropic reaction
Silyl ether
Simmons–Smith reaction
Skraup reaction
Smiles rearrangement
SN1 reaction
SN2 reaction
SNi
Solvolysis
Sommelet reaction
Sonogashira coupling
Staudinger reaction
Steglich esterification
Stephen aldehyde synthesis
Stetter reaction
Stevens rearrangement
Stieglitz rearrangement
Stille reaction
Stollé synthesis
Stork enamine alkylation
Strain (chemistry)
Strecker amino acid synthesis
Strecker degradation
Sulfonate
Sulfur mustard
Suzuki reaction
Swain equation
Swern oxidation
Sørensen formol titration
Takai olefination
Talk:Petasis reaction
Tebbe's reagent
Terephthalic acid
Tetralin
Tetrapropylammonium perruthenate
Triphenylmethyl radical
Tropinone
Tryptamine
Ullmann condensation
Urea
Wagner–Meerwein rearrangement
Willgerodt rearrangement
Wittig reaction
Wohl degradation
Wolffenstein–Böters reaction
Wulff–Dötz reaction
Zaitsev's rule
Étard reaction
1,4-Benzoquinone
Thiol-yne reaction
Thorpe reaction
Tiffeneau–Demjanov rearrangement
Tishchenko reaction
Aldol–Tishchenko reaction
Tollens' reagent
Transfer hydrogenation
Trapp mixture
Transesterification
Purine
Hydrolysis
Ugi reaction
Ullmann reaction
Upjohn dihydroxylation
Urech hydantoin synthesis
Van Slyke determination
Varrentrapp reaction
Vilsmeier–Haack reaction
Acyloin
Volhard–Erdmann cyclization
Von Braun amide degradation
Von Braun reaction
Cinnoline
Von Richter reaction
Wacker process
Wagner-Jauregg reaction
Walden inversion
Wallach rearrangement
Weerman degradation
Weinreb ketone synthesis
Wenker synthesis
Flavones
Westphalen–Lettré rearrangement
Wharton reaction
Whiting reaction
Wilkinson's catalyst
Williamson ether synthesis
2-Norbornyl cation
1,2-Wittig rearrangement
Wohl–Aue reaction
Wöhler synthesis
Wohl–Ziegler bromination
Wolff rearrangement
Wolff–Kishner reduction
Woodward cis-hydroxylation
Woodward–Hoffmann rules
Wurtz reaction
Wurtz–Fittig reaction
Yamaguchi esterification
Zeisel determination
Zerewitinoff determination
Disulfide
Zincke nitration
Zincke reaction
Zincke–Suhl reaction
Zinin reaction