Well-known reactions and reagents in organic chemistry include==0-9==*1,3-dipolar cycloaddition*2,3-Wittig rearrangement==A==*Abramovitch–Shapiro tryptamine synthesis*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*Auwers synthesis*Azo coupling==B==Ball reduction*Baeyer–Drewson indigo synthesis*Baeyer–Villiger oxidation*Baeyer–Villiger rearrangement*Bakeland process (Bakelite)*Baker–Venkataraman rearrangement, Baker–Venkataraman transformation*Bally–Scholl synthesis*Balz–Schiemann reaction*Bamberger rearrangement*Bamberger triazine synthesis*Bamford–Stevens reaction*Barbier–Wieland degradation*Bardhan–Sengupta phenanthrene synthesis*Barfoed's test*Bartoli indole synthesis, Bartoli reaction*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*Bodroux reaction*Bodroux–Chichibabin aldehyde synthesis*Bogert–Cook synthesis*Bohn–Schmidt reaction*Boord olefin synthesis*Borodin reaction*Borsche–Drechsel cyclization*Bosch–Meiser urea process*Bouveault aldehyde synthesis*Bouveault–Blanc reduction*Boyland–Sims oxidation*Boyer Reaction*Bredt's rule*Brown hydroboration*Bucherer carbazole synthesis*Bucherer reaction*Bucherer–Bergs reaction*Buchner ring enlargement*Büchner–Curtius–Schlotterbeck reaction*Buchwald–Hartwig amination*Bunnett reaction==C==*Cadiot–Chodkiewicz coupling*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*Corey–Gilman–Ganem oxidation*Cook–Heilbron thiazole synthesis*Cope elimination*Cope rearrangement*Corey reagent*Corey–Bakshi–Shibata reduction*Corey–Fuchs reaction*Corey–Kim oxidation*Corey–Posner, Whitesides–House reaction*Corey–Winter olefin synthesis*Corey–Winter reaction*Coupling 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*Dakin–West reaction*Danheiser Annulation*Darapsky degradation*Darzens condensation, Darzens–Claisen reaction, Glycidic ester condensation*Darzens halogenation*Darzens synthesis of unsaturated ketones*Darzens tetralin synthesis*Dehydration reaction*Dehydrogenation*Delepine 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-pi-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*Ene reaction*Enyne metathesis*Epoxidation*Erlenmeyer synthesis, Azlactone synthesis*Erlenmeyer–Plöchl azlactone and amino-acid synthesis*Eschenmoser fragmentation*Eschweiler–Clarke reaction*Ester pyrolysis*Ether cleavage*Étard reaction*Evans aldol==F==*Favorskii reaction*Favorskii rearrangement*Favorskii–Babayan synthesis*Fehling test*Feist–Benary synthesis*Fenton reaction*Ferrario reaction*Ferrier carbocyclization*Ferrier rearrangement*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*Free radical halogenation*Freund reaction*Friedel–Crafts acylation*Friedel–Crafts alkylation*Friedländer synthesis*Fries rearrangement*Fritsch–Buttenberg–Wiechell rearrangement*Fujimoto–Belleau 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*Gomberg–Bachmann reaction*Gomberg–Bachmann–Hey reaction*Gomberg free-radical reaction*Gould–Jacobs reaction*Graebe–Ullmann synthesis*Grignard degradation*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==*Haber–Weiss reaction*Haller–Bauer reaction*Haloform reaction*Halogen addition reaction*Halohydrin formation reaction*Hammett equation*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 ozonide reaction*Haworth methylation*Haworth Phenanthrene synthesis*Haworth reaction*Hay coupling*Hayashi rearrangement*Heck reaction*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*Hydration reaction*Hydroamination*Hydrodesulfurization*Hydrogenolysis*Hydrosilylation*Hinsberg indole synthesis*Hinsberg oxindole synthesis*Hinsberg reaction*Hinsberg separation*Hinsberg sulfone synthesis*Hoch–Campbell ethylenimine synthesis*Hock rearrangement*Hofmann degradation, Exhaustive methylation*Hofmann elimination*Hofmann Isonitrile synthesis, Carbylamine reaction*Hofmann produkt*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*Hydroboration*Hydrocarbon cracking*Hydrohalogenation==I==*Indium mediated allylation*Ing–Manske procedure*Ipso substitution*Ishikawa reagent*"trans-cis" isomerism*Ivanov reagent, Ivanov reaction==J==*Jacobsen epoxidation*Jacobsen rearrangement*Janovsky reaction*Japp–Klingemann reaction*Japp–Maitland condensation*Johnson–Claisen rearrangement*Jones oxidation*Jordan–Ullmann–Goldberg synthesis*Julia olefination*Julia–Lythgoe olefination==K==*Kabachnik–Fields reaction*Kharasch–Sosnovsky 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–Schmitt reaction*König method*Kornblum oxidation*Kornblum–DeLaMare rearrangement*Kostanecki acylation*Kowalski ester homologation*Krapcho decarboxylation*Kröhnke aldehyde synthesis*Kröhnke oxidation*Kröhnke pyridine synthesis*Kucherov reaction*Kuhn–Winterstein reaction*Kulinkovich reaction*Kumada coupling==L==*Larock indole synthesis*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*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*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*Methylation*Meyer and Hartmann reaction*Meyer reaction*Meyer synthesis*Meyer–Schuster rearrangement*Michael addition*Michael addition, Michael system*Michael condensation*Michaelis–Arbuzov reaction*Mignonac reaction*Milas hydroxylation of olefins*Minisci reaction*Mitsunobu reaction*Molisch's test*Mukaiyama aldol addition*Mukaiyama reaction*Myers' asymmetric alkylation==N==*Nametkin rearrangement*Nazarov cyclization reaction*Neber rearrangement*Nef reaction*Negishi coupling*Negishi zipper reaction*Nenitzescu indole synthesis*Nenitzescu reductive acylation*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*Ostromyslenskii reaction, Ostromisslenskii reaction*Oxidative decarboxylation*Oxo synthesis*Oxy-Cope rearrangement*Oxymercuration*Oxidation of secondary alcohols to ketones*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*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*Piria reaction*Pitzer strain*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==Q==*Quelet reaction==R==*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*Reilly–Hickinbottom rearrangement*Reimer–Tiemann reaction*Reissert indole synthesis*Reissert reaction, Reissert compound*Reppe synthesis*Retropinacol rearrangement*Rieche formylation*Riemschneider thiocarbamate synthesis*Riley oxidations*Rothemund synthesis*Ring closing metathesis*Ring opening metathesis*Ritter reaction*Robinson annulation*Robinson–Gabriel synthesis*Robinson Schopf reaction*Rosenmund reaction*Rosenmund reduction*Rosenmund–von Braun synthesis*Rothemund reaction*Rupe rearrangement*Rubottom oxidation*Ruff–Fenton degradation*Ruzicka large-ring synthesis==S==*Sakurai reaction*Salol reaction*Sandheimer*Sandmeyer diphenylurea isatin synthesis*Sandmeyer isonitrosoacetanilide isatin synthesis*Sandmeyer reaction*Sanger reagent*Saponification*Sarett oxidation*Saytzeff rule, Saytzeff's Rule*Schiemann reaction*Schiff reaction*Schiff test*Schlenk equilibrium*Schlosser modification*Schlosser variant*Schmidlin ketene synthesis*Schmidt degradation*Schmidt reaction*Scholl reaction*Schorigin Shorygin reaction, Shorygin reaction, Wanklyn reaction*Schotten–Baumann reaction*Seliwanoff's test*Semidine rearrangement*Semmler–Wolff reaction*Seyferth–Gilbert homologation*Shapiro reaction*Sharpless asymmetric dihydroxylation*Sharpless epoxidation*Sharpless oxyamination or aminohydroxylation*Shenck ene reaction*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*Staudinger reaction*Stephen aldehyde synthesis*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*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*Twitchell process*Tyrer sulfonation process==U==*Ugi reaction*Ullmann reaction*Upjohn dihydroxylation*Urech cyanohydrin method*Urech hydantoin synthesis==V==*Van Slyke determination*Varrentrapp reaction*Vilsmeier reaction*Vilsmeier–Haack reaction*Voight amination*Volhard–Erdmann cyclization*von Braun amide degradation*von Braun reaction*von Richter cinnoline synthesis*von Richter reaction==W==*Wacker–Tsuji oxidation*Wagner-Jauregg reaction*Wagner–Meerwein rearrangement*Waits–Scheffer epoxidation*Walden inversion*Wallach rearrangement*Weerman degradation*Weinreb ketone synthesis*Wenker ring closure*Wenker synthesis*Wessely–Moser rearrangement*Westphalen–Lettré rearrangement*Wharton reaction*Whiting reaction*Wichterle reaction*Widman–Stoermer synthesis*Wilkinson catalyst*Willgerodt rearrangement*Willgerodt–Kindler reaction*Williamson ether synthesis*Winstein reaction*Wittig reaction*Wittig rearrangement*Wittig–Horner reaction*Wohl degradation*Wohl–Aue reaction*Wohler synthesis*Wohl–Ziegler reaction*Wolffenstein–Böters reaction*Wolff rearrangement*Wolff–Kishner reduction*Woodward cis-hydroxylation*Woodward–Hoffmann rule*Wulff–Dötz reaction*Wurtz coupling, Wurtz reaction*Wurtz–Fittig reaction==Y==*Yamada–Okamoto purine synthesis*Yamaguchi esterification==Z==*Zeisel determination*Zerevitinov determination, Zerewitinoff determination*Ziegler condensation*Ziegler method*Zimmermann reaction*Zincke disulfide cleavage*Zinke nitration*Zincke reaction*Zincke–Suhl reaction*Zinin reduction==See also==* Name reaction* List of organic compounds* List of inorganic compounds* Named inorganic compounds* List of biomolecules* List of minerals== References ==== External links ==
در فهرست زیر تعدادی از واکنش‌های آلی شناخته شده بر اساس حرف اول نام انگلیسی آن فهرست شده است:*1,3-dipolar cycloaddition*2,3-Wittig rearrangement==A==*استال*Achmatowicz reaction*Acyloin condensation*کربوکسیل‌زدایی آدامز*واکنش ادکینز–پترسون*Akabori amino acid reaction*Alder ene reaction*واکنش آلدول*واکنش آلگار–فلین–اویامادا*Alkylimino-de-oxo-bisubstitution*Alkyne trimerisation*Alkyne zipper reaction*بازآرایی آلیلی*Amadori rearrangement*Amine alkylation*فرایند آندروسوف*واکنش مایکلز–آربوزوف, واکنش مایکلز–آربوزوف*Arens–van Dorp synthesis, Isler modification*Aromatic nitration*Arndt–Eistert synthesis*Auwers synthesis==B==*Baeyer–Drewson indigo synthesis*اکسایش بایر–ویلیگر*Baker–Venkataraman rearrangement, Baker–Venkataraman transformation*Bally–Scholl synthesis*Bamberger rearrangement*Bamberger triazine synthesis*Bamford–Stevens reaction*Bardhan–Sengupta phenanthrene synthesis*Barfoed's test*Bartoli indole synthesis, Bartoli reaction*واکنش بارتون–کلاگ*واکنش بارتون–زارد*Barton vinyl iodine procedure*Bayer test*Baylis–Hillman reaction*Bechamp reaction*Bechamp reduction*بازآرایی بکمان*Bellus–Claisen rearrangement*Benary reaction*واکنش بنکسر*Benzilic acid rearrangement*Benzoin condensation*Bergman cyclization*Bergmann azlactone peptide synthesis*Bergmann degradation*Bergmann–Zervas carbobenzoxy method*Bernthsen acridine synthesis*Bestmann's reagent*واکنش بیگینلی*Bingel reaction*Birch reduction*Bischler–Möhlau indole synthesis*Bischler–Napieralski reaction*Biuret test*واکنش بلیز*واکنش بلان*Bodroux–Chichibabin aldehyde synthesis*واکنش ولفن‌اشتین–بوترز*Boord olefin synthesis*کربازول*Bouveault aldehyde synthesis*Bouveault–Blanc reduction*Boyland–Sims oxidation*Bredt's rule*Brown hydroboration*Bucherer carbazole synthesis*واکنش بوخرر–برگز*Buchner ring enlargement*واکنش بوشوالد–هارت‌ویگ*Bunnett reaction==C==*Camps quinoline synthesis*Carbohydrate acetalisation*Carbonyl reduction*Carbonylation*Carbylamine reaction*Carroll reaction*Catalytic reforming*Catellani Reaction*CBS reduction*آمید*Cheletropic reaction*واکنش چی‌چی‌بابین*Chiral pool synthesis*پیریدین*Claisen rearrangement*Clemmensen reduction*Collins reagent*Combes quinoline synthesis*Conia reaction*Conrad–Limpach synthesis*سنتز تیازول کوک–هیلبرون*Cope elimination*Cope rearrangement*Corey reagent*Corey–Bakshi–Shibata reduction*Corey–Fuchs reaction*سنتز کوری–هوس*سنتز اولفین کوری–وینتر*ترکیبات دی‌آزونیم*Cram's rule of asymmetric induction*Creighton process*Criegee reaction*Criegee rearrangement*Crum Brown–Gibson rule*بازآرایی کورتیوس, بازآرایی کورتیوس*Cyanohydrin reaction==D==*واکنش داکین–وست*Danheiser Annulation*Darzens condensation, Darzens–Claisen reaction, Glycidic ester condensation*تترالین*Dehydration reaction*واکنش دلپین*Demjanov rearrangement*Demjanow desamination*Dess–Martin oxidation*Diazoalkane 1,3-dipolar cycloaddition*دی‌ایزوبوتیل‌آلومینیوم هیدرید*تراکم دیکمان*Diels–Reese reaction*Dienol benzene rearrangement*Dimroth rearrangement*Di-pi-methane rearrangement*Directed ortho metalation*Doebner modification*Doebner–Miller reaction, Beyer method for quinolines*Doering–LaFlamme carbon chain extension*Dötz reaction*Dowd–Beckwith ring expansion reaction*Duff reaction*Dyotropic reaction==E==*E1cB elimination reaction*جیوه (I) کلرید*Edman degradation*نیتروس بنزن*واکنش اینهورن–برونر*Elbs persulfate oxidation*Electrochemical fluorination*Electrocyclic reaction*Electrophilic halogenation*Electrophilic amination*Emde degradation*Ene reaction*Enyne metathesis*Erlenmeyer synthesis, Azlactone synthesis*Erlenmeyer–Plöchl azlactone and amino-acid synthesis*Eschenmoser fragmentation*Eschweiler–Clarke reaction*Ester pyrolysis*واکنش اتار==F==*Favorskii rearrangement*Favorskii–Babayan synthesis*Fehling test*Fenton reaction*Ferrier carbocyclization*Ferrier rearrangement*Finkelstein reaction*Fischer indole synthesis*Fischer oxazole synthesis*Fischer phenylhydrazine and oxazone reaction*Fischer glycosidation*Fischer–Hepp rearrangement*Fischer–Speier esterification*اکسیداسیون فلمینگ–تاما او*واکنشگر فولین دنیز–سیکالتو*Formox process*Forster reaction*Forster–Decker method*نیتریل*ترکیبات آلی روی*Free radical halogenation*واکنش فریدل–کرافتس*Friedländer synthesis*Fries rearrangement*Fujimoto–Belleau reaction*Fukuyama indole synthesis*Fukuyama reduction==G==*Gabriel synthesis*Gallagher–Hollander degradation*Gassman indole synthesis*واکنش گاترمان*واکنش گاترمان*Geminal halide hydrolysis*فتالیک انیدرید*جفت‌شدن گلیسر*Glycol cleavage*واکنش گومبرگ–باخمان*Gomberg free-radical reaction*Gould–Jacobs reaction*واکنشگر گرینیارد*Grob fragmentation*Groove synthesis*کاتالیزور گروبز in Olefin metathesis*فلوئوروکربن*Guerbet reaction==H==*Haber–Weiss reaction*واکنش هالوفرم*Halohydrin formation reaction*واکنش هامیک*Hammond principle or Hammond postulate*Hantzsch pyrrole synthesis*Hantzsch dihydropyridine synthesis, Hantzsch pyridine synthesis*Hantzsch pyridine synthesis, پیریدین, ۲-پیریدون, Knoevenagel–Fries modification*Hantzsch–Collidin synthesis*دی‌متیل سولفات*واکنش فریدل–کرافتس*Hayashi rearrangement*Helferich method*Hell–Volhard–Zelinsky halogenation*Hemetsberger indole synthesis*Hemetsberger–Knittel synthesis*Henry reaction, Kamlet reaction*Herz reaction, Herz compounds*رنگ نیل*Hydroamination*Hydrodesulfurization*Hydrogenolysis*Hydrosilylation*Hinsberg indole synthesis*Hinsberg oxindole synthesis*Hinsberg reaction*Hinsberg separation*Hinsberg sulfone synthesis*Hock rearrangement*حذف هافمن*ایزوسیانید, Carbylamine reaction*بازآرایی هافمن*Hofmann–Löffler reaction, Löffler–Freytag reaction, Hofmann–Löffler–Freytag reaction*Hofmann–Martius rearrangement*ترکیبات آلی جیوه*Homo rearrangement of steroids*Hooker reaction*Horner–Wadsworth–Emmons reaction*واکنش ساکورای*Hudlicky fluorination*Hydroboration*Hydrohalogenation==I==*Indium mediated allylation*Ing–Manske procedure*Ipso substitution*Ishikawa reagent*واکنش ایوانف, واکنش ایوانف==J==*Jacobsen epoxidation*Jacobsen rearrangement*Janovsky reaction*Japp–Klingemann reaction*Japp–Maitland condensation*Johnson–Claisen rearrangement*Jones oxidation*Julia olefination*Julia–Lythgoe olefination==K==*Kabachnik–Fields reaction*Kharasch–Sosnovsky reaction*Ketone halogenation*Kiliani–Fischer synthesis*Kindler reaction*Kishner cyclopropane synthesis*Knoevenagel condensation*Knorr pyrazole synthesis*Knorr pyrrole synthesis*Knorr quinoline synthesis*واکنش کچی*Koenigs–Knorr reaction*واکنش اشمیت-کلبه*König method*Kornblum oxidation*Kornblum–DeLaMare rearrangement*Kostanecki acylation*Kowalski ester homologation*Krapcho decarboxylation*واکنش ساملت*استیلن*Kulinkovich reaction==L==*Larock indole synthesis*Lehmstedt–Tanasescu reaction*Leimgruber–Batcho indole synthesis*Letts nitrile synthesis*Leuckart reaction*Leuckart thiophenol reaction*Leuckart–Wallach reaction*گاز خردل*واکنش هالوفرم, واکنش هالوفرم*ملامین*Lindlar catalyst*Lobry–de Bruyn–van Ekenstein transformation*Lossen rearrangement*Lucas' reagent*Luche reduction==M==*Maillard reaction*Madelung synthesis*Malaprade reaction, Periodic acid oxidation*Malonic ester synthesis*Mannich reaction*Markó–Lam deoxygenation*Martinet dioxindole synthesis*McDougall monoprotection*McFadyen–Stevens reaction*آریل‌دار کردن میروین*Meerwein–Ponndorf–Verley reduction*Meissenheimer complex*Menshutkin reaction*Metal-ion-catalyzed σ-bond rearrangement*Mesylation*متیل‌دار کردن*Meyer and Hartmann reaction*Meyer reaction*Meyer synthesis*Meyer–Schuster rearrangement*واکنش مایکل, واکنش مایکل*واکنش مایکلز–آربوزوف*Mignonac reaction*Milas hydroxylation of olefins*Minisci reaction*Mitsunobu reaction*Mukaiyama aldol addition*Myers' asymmetric alkylation==N==*Nametkin rearrangement*Nazarov cyclization reaction*Neber rearrangement*جفت‌شدن نگیشی*Negishi zipper reaction*Nenitzescu indole synthesis*Nicholas reaction*Niementowski quinazoline synthesis*Niementowski quinoline synthesis*Nierenstein reaction*NIH shift*Nitroaldol reaction*Nitrone-olefin 3+2 cycloaddition*Noyori asymmetric hydrogenation*Nucleophilic acyl substitution==O==*Ohira–Bestmann reaction*Olah reagent*Olefin metathesis*Oppenauer oxidation*Oxidative decarboxylation*Oxo synthesis*Oxy-Cope rearrangement*Oxymercuration*Oxidation of secondary alcohols to ketones==P==*Paal–Knorr pyrrole synthesis*Paal–Knorr synthesis*Paneth technique*واکنش پاترنو–بوچی*Payne rearrangement*پیرازول*نیتریل*Peptide synthesis*Perkin alicyclic synthesis*بنزوفوران*Petasis reaction*واکنش پیترسون*Petrenko-Kritschenko piperidone synthesis*Pfau–Plattner azulene synthesis*Pfitzinger reaction*Pfitzner–Moffatt oxidation*Piancatelli rearrangement*فنانتریدین*واکنش پیکتت–اسپنگلر*واکنش جفت‌شدن پیناکول*Pinacol rearrangement*واکنش پینر*Pinner triazine synthesis*Pitzer strain*ایزوکوئینولین*Prato reaction*Prelog strain*Prevost reaction*اپوکساید*Prinzbach synthesis*Protecting group*Pummerer rearrangement==Q==*Quelet reaction==R==*Ramberg–Bäcklund reaction*Raney nickel*Raschig phenol process*Rauhut–Currier reaction*Reductive amination*Reductive dehalogenation of halo ketones*Reed reaction*Reilly–Hickinbottom rearrangement*Reissert indole synthesis*Reissert reaction, Reissert compound*Reppe synthesis*Retropinacol rearrangement*Rieche formylation*Riemschneider thiocarbamate synthesis*Riley oxidations*Rothemund synthesis*Ring closing metathesis*Ring opening metathesis*Ritter reaction*Robinson annulation*Robinson–Gabriel synthesis*واکنش رزنموند*Rosenmund–von Braun synthesis*Rupe rearrangement*Rubottom oxidation*Ruff–Fenton degradation*Ruzicka large-ring synthesis==S==*فنول سالیسیلات*Sandheimer*Sandmeyer diphenylurea isatin synthesis*Sandmeyer isonitrosoacetanilide isatin synthesis*۱-فلوئورو-۴،۲-دی‌نیتروبنزن*Saponification*Sarett oxidation*واکنش بالز–شیمان*Schiff test*Schlenk equilibrium*واکنش ویتیگ*واکنش اشمیت*واکنش شول*Schorigin Shorygin reaction, Shorygin reaction, Wanklyn reaction*Seliwanoff's test*بازآرایی بکمان*Seyferth–Gilbert homologation*Shapiro reaction*Sharpless asymmetric dihydroxylation*Sharpless epoxidation*Sharpless oxyamination or aminohydroxylation*Shenck ene reaction*Sigmatropic reaction*Simmons–Smith reaction*تراکم پچمان*Simons process*Skraup chinolin synthesis*Skraup reaction*Smiles rearrangement*جانشینی هسته‌دوست آروماتیک nucleophilic aromatic substitution*واکنش SN1*واکنش SN2*SNi*Solvolysis*Sonn–Müller method*Sørensen formol titration*واکنش اشتودینگر*Stephen aldehyde synthesis*Stetter reaction*Stevens rearrangement*Stieglitz rearrangement*تراکم کلایزن*Stollé synthesis*واکنش انامین استورک*Strecker amino acid synthesis*Strecker degradation*Strecker synthesis*Swain equation*Swern oxidation==T==*Tafel rearrangement*Takai olefination*ترکیبات نیترو*Thiol-yne reaction*اکسیم*Tiffeneau ring enlargement reaction*Tiffeneau–Demjanov rearrangement*Tischtschenko reaction*Tishchenko reaction, Tishchenko–Claisen reaction*Tollens reagent*Transfer hydrogenation*Trapp mixture*Transesterification*Truce–Smiles rearrangement*سنتز پیریدین چی‌چی‌بابین*آبکافت==U==*واکنش اولمان*Upjohn dihydroxylation*Urech cyanohydrin method*Urech hydantoin synthesis==V==*Van Slyke determination*Varrentrapp reaction*Vilsmeier reaction*Vilsmeier–Haack reaction*Volhard–Erdmann cyclization*von Braun amide degradation*von Braun reaction*von Richter cinnoline synthesis*von Richter reaction==W==*Wacker–Tsuji oxidation*Wagner-Jauregg reaction*Wagner–Meerwein rearrangement*Walden inversion*Wallach rearrangement*Weerman degradation*Weinreb ketone synthesis*Wenker ring closure*Wenker synthesis*Wessely–Moser rearrangement*Westphalen–Lettré rearrangement*Wharton reaction*Whiting reaction*Wichterle reaction*Widman–Stoermer synthesis*Willgerodt rearrangement*Willgerodt–Kindler reaction*Winstein reaction*Wittig rearrangement*Wittig–Horner reaction*Wohl degradation*Wohl–Aue reaction*Wohl–Ziegler reaction*بازآرایی ولف*Woodward cis-hydroxylation*Woodward–Hoffmann rule*Wulff–Dötz reaction*Wurtz–Fittig reaction==Y==*Yamaguchi esterification==Z==*Zeisel determination*Zerevitinov determination, Zerewitinoff determination*واکنش تورپ*Zimmermann reaction*Zinke nitration*Zincke reaction*Zincke–Suhl reaction*Zinin reduction* فهرست ترکیب‌های معدنی* فهرست زیست‌مولکول‌ها* http://www.organic-chemistry.org/namedreactions/* http://www.synarchive.com/named-reactions* http://www.chem.wisc.edu/areas/reich/handouts/NameReagents/namedreag-cont.htm* http://www.name-reaction.com/list