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]] | ||
* [[: | * [[Polymerization]] | ||
* [[ | * [[:Category:Reagents for organic chemistry|Reagents]] | ||
* [[ | * [[Rearrangement reaction]] | ||
* [[ | * [[Organic redox reaction|Redox reaction]] | ||
* [[ | * [[Regioselectivity]] | ||
* [[ | * [[Stereoselectivity]] | ||
* [[ | * [[Stereospecificity]] | ||
* [[Substitution reaction]] | |||
|list2 = | |||
* [[A value]] | * [[A value]] | ||
* [[Alpha effect]] | * [[Alpha effect]] | ||
| Line 94: | Line 97: | ||
|title = [[List of organic reactions]] | |title = [[List of organic reactions]] | ||
| group1 = | | group1 = Carbon-carbon bond forming reactions | ||
| list1 = | |||
* [[Acetoacetic ester synthesis]] | * [[Acetoacetic ester synthesis]] | ||
* [[Acyloin condensation]] | * [[Acyloin condensation]] | ||
| Line 231: | Line 235: | ||
* [[Zincke–Suhl 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]] | * [[1,3-Dipolar cycloaddition]] | ||
* [[Annulation]] | * [[Annulation]] | ||
| Line 554: | Line 582: | ||
* [[Wenker synthesis]] | * [[Wenker synthesis]] | ||
{{Navbox|child| | {{Navbox|child| | ||
| group1 =[[ | | 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> | </noinclude> | ||
Latest revision as of 15:33, 12 December 2022
