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wikipedia>DMacks: direc

2022-11-06T20:01:17Z

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alpha>Indicwiki at 07:05, 28 October 2022

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alpha>Indicwiki at 07:01, 28 October 2022

2022-10-28T07:01:14Z

← Older revision		Revision as of 12:31, 28 October 2022
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	{{Navbox		{{Navbox
	\|name =कार्बनिक प्रतिक्रियाएँ		\|name =कार्बनिक प्रतिक्रियाएँ
	\|title =[[कार्बनिक प्रतिक्रिया \| कार्बनिक प्रतिक्रियाओं] में विषय		\|title =[[कार्बनिक प्रतिक्रिया \| कार्बनिक प्रतिक्रियाओं]] में विषय
	\|listclass = hlist		\|listclass = hlist
	\|list1 =* [[इसके अलावा प्रतिक्रिया]]		\|list1 =* [[इसके अलावा प्रतिक्रिया]]
	* [[उन्मूलन प्रतिक्रिया]]		* [[उन्मूलन प्रतिक्रिया]]
	* [[पोलीमराइजेशन]]		* [[पोलीमराइजेशन]]
	* [[: ~~श्रेणी~~: कार्बनिक रसायन विज्ञान के लिए अभिकर्मक \| अभिकर्मक]]		* [[:Category: कार्बनिक रसायन विज्ञान के लिए अभिकर्मक \| अभिकर्मक]]
	* [[पुनर्व्यवस्थित प्रतिक्रिया]]		* [[पुनर्व्यवस्थित प्रतिक्रिया]]
	* [[कार्बनिक रेडॉक्स प्रतिक्रिया \| रेडॉक्स प्रतिक्रिया]]		* [[कार्बनिक रेडॉक्स प्रतिक्रिया \| रेडॉक्स प्रतिक्रिया]]
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	}}		}}
	}}}}<noinclude>		}}}}<noinclude>
	~~[[Category:Organic chemistry navigational boxes]]~~

	</noinclude>		</noinclude>

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alpha>Indicwiki at 06:58, 28 October 2022

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alpha>Sarika: Created page with "{{Navbox |name = Organic reactions |title = Topics in organic reactions |listclass = hlist |list1 = * Addition reaction * Elimination reaction *..."

2022-10-28T06:53:58Z

Created page with "{{Navbox |name = Organic reactions |title = Topics in organic reactions |listclass = hlist |list1 = * Addition reaction * Elimination reaction *..."

New page

{{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 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]]
* [[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 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-pi-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]]

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Template:Organic reactions - Revision history

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alpha>Indicwiki at 07:05, 28 October 2022

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alpha>Indicwiki at 06:58, 28 October 2022

alpha>Sarika: Created page with "{{Navbox |name = Organic reactions |title = Topics in organic reactions |listclass = hlist |list1 = * Addition reaction * Elimination reaction *..."