Template:Organic reactions: Difference between revisions
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{{Navbox | {{Navbox | ||
|name = | |name = Organic reactions | ||
|title =[[ | |title = Topics in [[Organic reaction|organic reactions]] | ||
|listclass = hlist | |listclass = hlist | ||
|list1 =* [[ | |list1 = | ||
* [[ | * [[Addition reaction]] | ||
* [[ | * [[Elimination reaction]] | ||
* [[:Category: | * [[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]] | ||
* [[2- | * [[More O'Ferrall–Jencks plot]] | ||
* [[ | * [[Negative hyperconjugation]] | ||
* [[ | * [[Neighbouring group participation]] | ||
* [[ | * [[2-Norbornyl cation]] | ||
* [[ | * [[Nucleophile]] | ||
* [[ | * [[Kennedy J. P. Orton]] | ||
* [[ | * [[Passive binding]] | ||
* [[ | * [[Phosphaethynolate]] | ||
* [[Σ- | * [[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]] | ||
* [[Σ- | * [[Y-aromaticity]] | ||
* [[Yukawa–Tsuno equation]] | |||
* [[Zaitsev's rule]] | |||
* [[Σ-bishomoaromaticity]] | |||
{{Navbox |child | {{Navbox |child | ||
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|title = [[List of organic reactions]] | |title = [[List of organic reactions]] | ||
| group1 = | | group1 = Carbon-carbon bond forming 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]] | ||
* [[Reformatsky | * [[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| | {{Navbox|child| | ||
| group1 =[[ | | 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 bond forming 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 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]]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]]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]]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]] | |||
* [[Imine 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]] | [[Category:Organic chemistry navigational boxes]] | ||
</noinclude> | |||
Revision as of 01:31, 7 November 2022
