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Your current IP address is 8.222.208.146. </p> <div class="paragraphbreak" style="margin-top:0.5em"></div><div style="font-size: 16px;"> <p>Even while globally blocked, you will <i>usually</i> still be able to edit pages on <a href="https://meta.wikimedia.org/wiki/" class="extiw" title="m:">Meta-Wiki</a>. </p> </div> <div class="paragraphbreak" style="margin-top:0.5em"></div><div style="font-size: 16px;"> <p>If you believe you were blocked by mistake, you can find additional information and instructions in the <a href="https://meta.wikimedia.org/wiki/Special:MyLanguage/No_open_proxies" class="extiw" title="m:Special:MyLanguage/No open proxies">No open proxies</a> global policy. Otherwise, to discuss the block please <a href="https://meta.wikimedia.org/wiki/Steward_requests/Global" class="extiw" title="m:Steward requests/Global">post a request for review on Meta-Wiki</a>. You could also send an email to the <a href="https://meta.wikimedia.org/wiki/Special:MyLanguage/Stewards" class="extiw" title="m:Special:MyLanguage/Stewards">stewards</a> <a href="https://meta.wikimedia.org/wiki/Special:MyLanguage/VRT" class="extiw" title="m:Special:MyLanguage/VRT">VRT</a> queue at <kbd>stewards@wikimedia.org</kbd> including all above details. </p> </div> <p>Other useful links: <a href="https://meta.wikimedia.org/wiki/Global_blocks" class="extiw" title="m:Global blocks">Global blocks</a> · <a href="/wiki/Help:I_have_been_blocked" title="Help:I have been blocked">Help:I have been blocked</a> </p> </div></li></ul><hr /> <div id="viewsourcetext">You can view and copy the source of this page:</div><textarea readonly="" accesskey="," id="wpTextbox1" cols="80" rows="25" style="" class="mw-editfont-monospace" lang="en" dir="ltr" name="wpTextbox1">{{Navbox |name = Organic reactions |title = Topics in [[Organic reaction|organic reactions]] |listclass = hlist |list1 = * [[Addition reaction]] * [[Elimination reaction]] * [[Polymerization]] * [[:Category:Reagents for organic chemistry|Reagents]] * [[Rearrangement reaction]] * [[Organic redox reaction|Redox reaction]] * [[Regioselectivity]] * [[Stereoselectivity]] * [[Stereospecificity]] * [[Substitution reaction]] |list2 = * [[A value]] * [[Alpha effect]] * [[Annulene]] * [[Anomeric effect]] * [[Antiaromaticity]] * [[Aromatic ring current]] * [[Aromaticity]] * [[Baird's rule]] * [[Baker–Nathan effect]] * [[Baldwin's rules]] * [[Bema Hapothle]] * [[Beta-silicon effect]] * [[Bicycloaromaticity]] * [[Bredt's rule]] * [[Bürgi–Dunitz angle]] * [[Catalytic resonance theory]] * [[Charge remote fragmentation]] * [[Charge-transfer complex]] * [[Clar's rule]] * [[Conformational isomerism]] * [[Conjugated system]] * [[Conrotatory and disrotatory]] * [[Curtin–Hammett principle]] * [[Dynamic binding (chemistry)]] * [[Edwards equation]] * [[Effective molarity]] * [[Electromeric effect]] * [[Electron-rich]] * [[Electron-withdrawing group]] * [[Electronic effect]] * [[Electrophile]] * [[Evelyn effect]] * [[Flippin–Lodge angle]] * [[Free-energy relationship]] * [[Grunwald–Winstein equation]] * [[Hammett acidity function]] * [[Hammett equation]] * [[George S. Hammond]] * [[Hammond's postulate]] * [[Homoaromaticity]] * [[Hückel's rule]] * [[Hyperconjugation]] * [[Inductive effect]] * [[Kinetic isotope effect]] * [[LFER solvent coefficients (data page)]] * [[Marcus theory]] * [[Markovnikov's rule]] * [[Möbius aromaticity]] * [[Möbius–Hückel concept]] * [[More O'Ferrall–Jencks plot]] * [[Negative hyperconjugation]] * [[Neighbouring group participation]] * [[2-Norbornyl cation]] * [[Nucleophile]] * [[Kennedy J. P. Orton]] * [[Passive binding]] * [[Phosphaethynolate]] * [[Polar effect]] * [[Polyfluorene]] * [[Ring strain]] * [[Σ-aromaticity]] * [[Spherical aromaticity]] * [[Spiroaromaticity]] * [[Steric effects]] * [[Superaromaticity]] * [[Swain–Lupton equation]] * [[Taft equation]] * [[Thorpe–Ingold effect]] * [[Vinylogy]] * [[Walsh diagram]] * [[Woodward–Hoffmann rules]] * [[Woodward's rules]] * [[Y-aromaticity]] * [[Yukawa–Tsuno equation]] * [[Zaitsev's rule]] * [[Σ-bishomoaromaticity]] {{Navbox |child |groupwidth=7.5em |title = [[List of organic reactions]] | group1 = Carbon-carbon <br> bond forming <br> reactions | list1 = * [[Acetoacetic ester synthesis]] * [[Acyloin condensation]] * [[Aldol condensation]] * [[Aldol reaction]] * [[Alkane metathesis]] * [[Alkyne metathesis]] * [[Alkyne trimerisation]] * [[Alkynylation]] * [[Allan–Robinson reaction]] * [[Arndt–Eistert reaction]] * [[Auwers synthesis]] * [[Aza-Baylis–Hillman reaction]] * [[Barbier reaction]] * [[Barton–Kellogg reaction]] * [[Baylis–Hillman reaction]] * [[Benary reaction]] * [[Bergman cyclization]] * [[Biginelli reaction]] * [[Bingel reaction]] * [[Blaise ketone synthesis]] * [[Blaise reaction]] * [[Blanc chloromethylation]] * [[Bodroux–Chichibabin aldehyde synthesis]] * [[Bouveault aldehyde synthesis]] * [[Bucherer–Bergs reaction]] * [[Buchner ring expansion]] * [[Cadiot–Chodkiewicz coupling]] * [[Carbonyl allylation]] * [[Carbonyl olefin metathesis]] * [[Castro–Stephens coupling]] * [[Chan rearrangement]] * [[Chan–Lam coupling]] * [[Claisen condensation]] * [[Claisen rearrangement]] * [[Claisen-Schmidt condensation]] * [[Combes quinoline synthesis]] * [[Corey–Fuchs reaction]] * [[Corey–House synthesis]] * [[Coupling reaction]] * [[Cross-coupling reaction]] * [[Cross dehydrogenative coupling]] * [[Cross-coupling partner]] * [[Dakin–West reaction]] * [[Darzens reaction]] * [[Diels–Alder reaction]] * [[Doebner reaction]] * [[Wulff–Dötz reaction]] * [[Ene reaction]] * [[Enyne metathesis]] * [[Ethenolysis]] * [[Favorskii reaction]] * [[Ferrier carbocyclization]] * [[Friedel–Crafts reaction]] * [[Fujimoto–Belleau reaction]] * [[Fujiwara–Moritani reaction]] * [[Fukuyama coupling]] * [[Gabriel–Colman rearrangement]] * [[Gattermann reaction]] * [[Glaser coupling]] * [[Grignard reaction]] * [[Grignard reagent]] * [[Hammick reaction]] * [[Heck reaction]] * [[Henry reaction]] * [[Heterogeneous metal catalyzed cross-coupling]] * [[High dilution principle]] * [[Hiyama coupling]] * [[Homologation reaction]] * [[Horner–Wadsworth–Emmons reaction]] * [[Hydrocyanation]] * [[Hydrovinylation]] * [[Hydroxymethylation]] * [[Ivanov reaction]] * [[Johnson–Corey–Chaykovsky reaction]] * [[Julia olefination]] * [[Julia–Kocienski olefination]] * [[Kauffmann olefination]] * [[Knoevenagel condensation]] * [[Knorr pyrrole synthesis]] * [[Kolbe–Schmitt reaction]] * [[Kowalski ester homologation]] * [[Kulinkovich reaction]] * [[Kumada coupling]] * [[Liebeskind–Srogl coupling]] * [[Malonic ester synthesis]] * [[Mannich reaction]] * [[McMurry reaction]] * [[Meerwein arylation]] * [[Methylenation]] * [[Michael reaction]] * [[Minisci reaction]] * [[Mizoroki-Heck vs. Reductive Heck]] * [[Nef isocyanide reaction]] * [[Nef synthesis]] * [[Negishi coupling]] * [[Nierenstein reaction]] * [[Nitro-Mannich reaction]] * [[Nozaki–Hiyama–Kishi reaction]] * [[Olefin conversion technology]] * [[Olefin metathesis]] * [[Palladium–NHC complex]] * [[Passerini reaction]] * [[Peterson olefination]] * [[Pfitzinger reaction]] * [[Piancatelli rearrangement]] * [[Pinacol coupling reaction]] * [[Prins reaction]] * [[Quelet reaction]] * [[Ramberg–Bäcklund reaction]] * [[Rauhut–Currier reaction]] * [[Reformatsky reaction]] * [[Reimer–Tiemann reaction]] * [[Rieche formylation]] * [[Ring-closing metathesis]] * [[Robinson annulation]] * [[Sakurai reaction]] * [[Seyferth–Gilbert homologation]] * [[Shapiro reaction]] * [[Sonogashira coupling]] * [[Stetter reaction]] * [[Stille reaction]] * [[Stollé synthesis]] * [[Stork enamine alkylation]] * [[Suzuki reaction]] * [[Takai olefination]] * [[Thermal rearrangement of aromatic hydrocarbons]] * [[Thorpe reaction]] * [[Ugi reaction]] * [[Ullmann reaction]] * [[Wagner-Jauregg reaction]] * [[Weinreb ketone synthesis]] * [[Wittig reaction]] * [[Wurtz reaction]] * [[Wurtz–Fittig reaction]] * [[Zincke–Suhl reaction]] {{Navbox|child| | group1 = [[Homologation reactions]] | list1 = * [[Arndt–Eistert reaction]] * [[Hooker reaction]] * [[Kiliani–Fischer synthesis]] * [[Kowalski ester homologation]] * [[Methoxymethylenetriphenylphosphorane]] * [[Seyferth–Gilbert homologation]] * [[Wittig reaction]] | group2 = Olefination reactions | list2 = * [[Bamford–Stevens reaction]] * [[Barton–Kellogg reaction]] * [[Boord olefin synthesis]] * [[Chugaev elimination]] * [[Cope reaction]] * [[Corey–Winter olefin synthesis]] * [[Dehydrohalogenation]] * [[Elimination reaction]] * [[Grieco elimination]] * [[Hofmann elimination]] * [[Horner–Wadsworth–Emmons reaction]] * [[Hydrazone iodination]] * [[Julia olefination]] * [[Julia–Kocienski olefination]] * [[Kauffmann olefination]] * [[McMurry reaction]] * [[Peterson olefination]] * [[Ramberg–Bäcklund reaction]] * [[Shapiro reaction]] * [[Takai olefination]] * [[Wittig reaction]] }} | group2 = Carbon-heteroatom <br> bond forming <br> reactions | list2 = * [[Azo coupling]] * [[Bartoli indole synthesis]] * [[Boudouard reaction]] * [[Cadogan–Sundberg indole synthesis]] * [[Diazonium compound]] * [[Esterification]] * [[Grignard reagent]] * [[Haloform reaction]] * [[Hegedus indole synthesis]] * [[Hurd–Mori 1,2,3-thiadiazole synthesis]] * [[Kharasch–Sosnovsky reaction]] * [[Knorr pyrrole synthesis]] * [[Leimgruber–Batcho indole synthesis]] * [[Mukaiyama hydration]] * [[Nenitzescu indole synthesis]] * [[Oxymercuration reaction]] * [[Reed reaction]] * [[Schotten–Baumann reaction]] * [[Ullmann condensation]] * [[Williamson ether synthesis]] * [[Yamaguchi esterification]] | group3 = Degradation <br> reactions | list3 = * [[Barbier–Wieland degradation]] * [[Bergmann degradation]] * [[Edman degradation]] * [[Emde degradation]] * [[Gallagher–Hollander degradation]] * [[Hofmann rearrangement]] * [[Hooker reaction]] * [[Isosaccharinic acid]] * [[Marker degradation]] * [[Ruff degradation]] * [[Strecker degradation]] * [[Von Braun amide degradation]] * [[Weerman degradation]] * [[Wohl degradation]] | group4 = [[Organic redox reaction|Organic redox <br> reaction]]s | list4 = * [[Acyloin condensation]] * [[Adkins–Peterson reaction]] * [[Akabori amino-acid reaction]] * [[Alcohol oxidation]] * [[Algar–Flynn–Oyamada reaction]] * [[Amide reduction]] * [[Andrussow process]] * [[Angeli–Rimini reaction]] * [[Aromatization]] * [[Autoxidation]] * [[Baeyer–Villiger oxidation]] * [[Barton–McCombie deoxygenation]] * [[Bechamp reduction]] * [[Benkeser reaction]] * [[Bergmann degradation]] * [[Birch reduction]] * [[Bohn–Schmidt reaction]] * [[Bosch reaction]] * [[Bouveault–Blanc reduction]] * [[Boyland–Sims oxidation]] * [[Cannizzaro reaction]] * [[Carbonyl reduction]] * [[Clemmensen reduction]] * [[Collins oxidation]] * [[Corey–Itsuno reduction]] * [[Corey–Kim oxidation]] * [[Corey–Winter olefin synthesis]] * [[Criegee oxidation]] * [[Dakin oxidation]] * [[Davis oxidation]] * [[Deoxygenation]] * [[Dess–Martin oxidation]] * [[DNA oxidation]] * [[Elbs persulfate oxidation]] * [[Emde degradation]] * [[Eschweiler–Clarke reaction]] * [[Étard reaction]] * [[Fischer–Tropsch process]] * [[Fleming–Tamao oxidation]] * [[Fukuyama reduction]] * [[Ganem oxidation]] * [[Glycol cleavage]] * [[Griesbaum coozonolysis]] * [[Grundmann aldehyde synthesis]] * [[Haloform reaction]] * [[Hydrogenation]] * [[Hydrogenolysis]] * [[Hydroxylation]] * [[Jones oxidation]] * [[Kiliani–Fischer synthesis]] * [[Kolbe electrolysis]] * [[Kornblum oxidation]] * [[Kornblum–DeLaMare rearrangement]] * [[Leuckart reaction]] * [[Ley oxidation]] * [[Lindgren oxidation]] * [[Lipid peroxidation]] * [[Lombardo methylenation]] * [[Luche reduction]] * [[Markó–Lam deoxygenation]] * [[McFadyen–Stevens reaction]] * [[Meerwein–Ponndorf–Verley reduction]] * [[Methionine sulfoxide]] * [[Miyaura borylation]] * [[Mozingo reduction]] * [[Noyori asymmetric hydrogenation]] * [[Omega oxidation]] * [[Oppenauer oxidation]] * [[Oxygen rebound mechanism]] * [[Ozonolysis]] * [[Parikh–Doering oxidation]] * [[Pinnick oxidation]] * [[Prévost reaction]] * [[Reduction of nitro compounds]] * [[Reductive amination]] * [[Riley oxidation]] * [[Rosenmund reduction]] * [[Rubottom oxidation]] * [[Sabatier reaction]] * [[Sarett oxidation]] * [[Selenoxide elimination]] * [[Shapiro reaction]] * [[Sharpless asymmetric dihydroxylation]] * [[Epoxidation of allylic alcohols]] * [[Sharpless epoxidation]] * [[Sharpless oxyamination]] * [[Stahl oxidation]] * [[Staudinger reaction]] * [[Stephen aldehyde synthesis]] * [[Swern oxidation]] * [[Transfer hydrogenation]] * [[Wacker process]] * [[Wharton reaction]] * [[Whiting reaction]] * [[Wohl–Aue reaction]] * [[Wolff–Kishner reduction]] * [[Wolffenstein–Böters reaction]] * [[Zinin reaction]] | group5 = [[Rearrangement reaction|Rearrangement <br> reaction]]s | list5 = * [[1,2-rearrangement]] * [[1,2-Wittig rearrangement]] * [[2,3-sigmatropic rearrangement]] * [[2,3-Wittig rearrangement]] * [[Achmatowicz reaction]] * [[Alkyne zipper reaction]] * [[Allen–Millar–Trippett rearrangement]] * [[Allylic rearrangement]] * [[Alpha-ketol rearrangement]] * [[Amadori rearrangement]] * [[Arndt–Eistert reaction]] * [[Aza-Cope rearrangement]] * [[Baker–Venkataraman rearrangement]] * [[Bamberger rearrangement]] * [[Banert cascade]] * [[Beckmann rearrangement]] * [[Benzilic acid rearrangement]] * [[Bergman cyclization]] * [[Bergmann degradation]] * [[Boekelheide reaction]] * [[Brook rearrangement]] * [[Buchner ring expansion]] * [[Carroll rearrangement]] * [[Chan rearrangement]] * [[Claisen rearrangement]] * [[Cope rearrangement]] * [[Corey–Fuchs reaction]] * [[Cornforth rearrangement]] * [[Criegee rearrangement]] * [[Curtius rearrangement]] * [[Demjanov rearrangement]] * [[Di-π-methane rearrangement]] * [[Dimroth rearrangement]] * [[Divinylcyclopropane-cycloheptadiene rearrangement]] * [[Dowd–Beckwith ring-expansion reaction]] * [[Electrocyclic reaction]] * [[Ene reaction]] * [[Enyne metathesis]] * [[Favorskii reaction]] * [[Favorskii rearrangement]] * [[Ferrier carbocyclization]] * [[Ferrier rearrangement]] * [[Fischer–Hepp rearrangement]] * [[Fries rearrangement]] * [[Fritsch–Buttenberg–Wiechell rearrangement]] * [[Gabriel–Colman rearrangement]] * [[Group transfer reaction]] * [[Halogen dance rearrangement]] * [[Hayashi rearrangement]] * [[Hofmann rearrangement]] * [[Hofmann–Martius rearrangement]] * [[Ireland–Claisen rearrangement]] * [[Jacobsen rearrangement]] * [[Kornblum–DeLaMare rearrangement]] * [[Kowalski ester homologation]] * [[Lobry de Bruyn–Van Ekenstein transformation]] * [[Lossen rearrangement]] * [[McFadyen–Stevens reaction]] * [[McLafferty rearrangement]] * [[Meyer–Schuster rearrangement]] * [[Mislow–Evans rearrangement]] * [[Mumm rearrangement]] * [[Myers allene synthesis]] * [[Nazarov cyclization reaction]] * [[Neber rearrangement]] * [[Newman–Kwart rearrangement]] * [[Overman rearrangement]] * [[Oxy-Cope rearrangement]] * [[Pericyclic reaction]] * [[Piancatelli rearrangement]] * [[Pinacol rearrangement]] * [[Pummerer rearrangement]] * [[Ramberg–Bäcklund reaction]] * [[Ring expansion and contraction]] * [[Ring-closing metathesis]] * [[Rupe reaction]] * [[Schmidt reaction]] * [[Semipinacol rearrangement]] * [[Seyferth–Gilbert homologation]] * [[Sigmatropic reaction]] * [[Skattebøl rearrangement]] * [[Smiles rearrangement]] * [[Sommelet–Hauser rearrangement]] * [[Stevens rearrangement]] * [[Stieglitz rearrangement]] * [[Thermal rearrangement of aromatic hydrocarbons]] * [[Tiffeneau–Demjanov rearrangement]] * [[Vinylcyclopropane rearrangement]] * [[Wagner–Meerwein rearrangement]] * [[Wallach rearrangement]] * [[Weerman degradation]] * [[Westphalen–Lettré rearrangement]] * [[Willgerodt rearrangement]] * [[Wolff rearrangement]] | group6 = [[Ring forming reaction|Ring forming <br> reaction]]s | list6 = * [[1,3-Dipolar cycloaddition]] * [[Annulation]] * [[Azide-alkyne Huisgen cycloaddition]] * [[Baeyer–Emmerling indole synthesis]] * [[Bartoli indole synthesis]] * [[Bergman cyclization]] * [[Biginelli reaction]] * [[Bischler–Möhlau indole synthesis]] * [[Bischler–Napieralski reaction]] * [[Blum–Ittah aziridine synthesis]] * [[Bobbitt reaction]] * [[Bohlmann–Rahtz pyridine synthesis]] * [[Borsche–Drechsel cyclization]] * [[Bucherer carbazole synthesis]] * [[Bucherer–Bergs reaction]] * [[Cadogan–Sundberg indole synthesis]] * [[Camps quinoline synthesis]] * [[Chichibabin pyridine synthesis]] * [[Cook–Heilbron thiazole synthesis]] * [[Cycloaddition]] * [[Darzens reaction]] * [[Davis–Beirut reaction]] * [[De Kimpe aziridine synthesis]] * [[Debus–Radziszewski imidazole synthesis]] * [[Dieckmann condensation]] * [[Diels–Alder reaction]] * [[Feist–Benary synthesis]] * [[Ferrario–Ackermann reaction]] * [[Fiesselmann thiophene synthesis]] * [[Fischer indole synthesis]] * [[Fischer oxazole synthesis]] * [[Friedländer synthesis]] * [[Gewald reaction]] * [[Graham reaction]] * [[Hantzsch pyridine synthesis]] * [[Hegedus indole synthesis]] * [[Hemetsberger indole synthesis]] * [[Hofmann–Löffler reaction]] * [[Hurd–Mori 1,2,3-thiadiazole synthesis]] * [[Iodolactonization]] * [[Isay reaction]] * [[Jacobsen epoxidation]] * [[Johnson–Corey–Chaykovsky reaction]] * [[Knorr pyrrole synthesis]] * [[Knorr quinoline synthesis]] * [[Kröhnke pyridine synthesis]] * [[Kulinkovich reaction]] * [[Larock indole synthesis]] * [[Madelung synthesis]] * [[Nazarov cyclization reaction]] * [[Nenitzescu indole synthesis]] * [[Niementowski quinazoline synthesis]] * [[Niementowski quinoline synthesis]] * [[Paal–Knorr synthesis]] * [[Paternò–Büchi reaction]] * [[Pechmann condensation]] * [[Petrenko-Kritschenko piperidone synthesis]] * [[Pictet–Spengler reaction]] * [[Pomeranz–Fritsch reaction]] * [[Prilezhaev reaction]] * [[Pschorr cyclization]] * [[Reissert indole synthesis]] * [[Ring-closing metathesis]] * [[Robinson annulation]] * [[Sharpless epoxidation]] * [[Simmons–Smith reaction]] * [[Skraup reaction]] * [[Urech hydantoin synthesis]] * [[Van Leusen reaction]] * [[Wenker synthesis]] {{Navbox|child| | group1 = [[Cycloaddition]] | list1 = * [[1,3-Dipolar cycloaddition]] * [[4+4 Photocycloaddition]] * [[(4+3) cycloaddition]] * [[6+4 Cycloaddition]] * [[Alkyne trimerisation]] * [[Aza-Diels–Alder reaction]] * [[Azide-alkyne Huisgen cycloaddition]] * [[Bradsher cycloaddition]] * [[Cheletropic reaction]] * [[Conia-ene reaction]] * [[Cyclopropanation]] * [[Diazoalkane 1,3-dipolar cycloaddition]] * [[Diels–Alder reaction]] * [[Enone–alkene cycloadditions]] * [[Hexadehydro Diels–Alder reaction]] * [[Intramolecular Diels–Alder cycloaddition]] * [[Inverse electron-demand Diels–Alder reaction]] * [[Ketene cycloaddition]] * [[McCormack reaction]] * [[Metal-centered cycloaddition reactions]] * [[Nitrone-olefin (3+2) cycloaddition]] * [[Oxo-Diels–Alder reaction]] * [[Ozonolysis]] * [[Pauson–Khand reaction]] * [[Povarov reaction]] * [[Prato reaction]] * [[Retro-Diels–Alder reaction]] * [[Staudinger synthesis]] * [[Trimethylenemethane cycloaddition]] * [[Vinylcyclopropane (5+2) cycloaddition]] * [[Wagner-Jauregg reaction]] | group2 = Heterocycle forming reactions | list2 = * [[Algar–Flynn–Oyamada reaction]] * [[Allan–Robinson reaction]] * [[Auwers synthesis]] * [[Bamberger triazine synthesis]] * [[Banert cascade]] * [[Barton–Zard reaction]] * [[Bernthsen acridine synthesis]] * [[Bischler–Napieralski reaction]] * [[Bobbitt reaction]] * [[Boger pyridine synthesis]] * [[Borsche–Drechsel cyclization]] * [[Bucherer carbazole synthesis]] * [[Bucherer–Bergs reaction]] * [[Chichibabin pyridine synthesis]] * [[Cook–Heilbron thiazole synthesis]] * [[Diazoalkane 1,3-dipolar cycloaddition]] * [[Einhorn–Brunner reaction]] * [[Erlenmeyer–Plöchl azlactone and amino-acid synthesis]] * [[Feist–Benary synthesis]] * [[Fischer oxazole synthesis]] * [[Gabriel–Colman rearrangement]] * [[Gewald reaction]] * [[Hantzsch ester]] * [[Hantzsch pyridine synthesis]] * [[Herz reaction]] * [[Knorr pyrrole synthesis]] * [[Kröhnke pyridine synthesis]] * [[Lectka enantioselective beta-lactam synthesis]] * [[Lehmstedt–Tanasescu reaction]] * [[Niementowski quinazoline synthesis]] * [[Nitrone-olefin (3+2) cycloaddition]] * [[Paal–Knorr synthesis]] * [[Pellizzari reaction]] * [[Pictet–Spengler reaction]] * [[Pomeranz–Fritsch reaction]] * [[Prilezhaev reaction]] * [[Robinson–Gabriel synthesis]] * [[Stollé synthesis]] * [[Urech hydantoin synthesis]] * [[Wenker synthesis]] * [[Wohl–Aue reaction]] }} }} }}<noinclude> [[Category:Organic chemistry navigational boxes]] </noinclude> </textarea><div class="templatesUsed"><div class="mw-templatesUsedExplanation"><p><span id="templatesused">Pages transcluded onto the current version of 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