User:Amitosh.swain/Books/Reactions of Organic Chemistry

Reactions of Organic Chemistry
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Collection of Organic Reactions

 * Organic reaction


 * Substitution Reactions
 * Substitution reaction
 * SN1 reaction
 * Sn1CB mechanism
 * SN2 reaction
 * SNi
 * Carbonyl Alpha-Substitution Reactions
 * Electrophilic substitution
 * Nucleophilic substitution
 * Aminolysis
 * Appel reaction
 * Aromatic sulfonation
 * Associative substitution
 * Azo coupling
 * Bechamp reaction
 * Benary reaction
 * Blanc chloromethylation
 * Bucherer reaction
 * Buchwald–Hartwig amination
 * Cadiot–Chodkiewicz coupling
 * Dakin–West reaction
 * Deamidation
 * Deamination
 * Decarboxylation
 * Delépine reaction
 * Directed ortho metalation
 * Electrophilic aromatic substitution
 * Electrophilic fluorination
 * Electrophilic halogenation
 * Ether cleavage
 * Finkelstein reaction
 * Fischer glycosidation
 * Forster–Decker method
 * Friedel–Crafts reaction
 * Gabriel synthesis
 * Geminal halide hydrolysis
 * Gomberg–Bachmann reaction
 * Heck reaction
 * Hell–Volhard–Zelinsky halogenation
 * Hoesch reaction
 * Hofmann–Löffler reaction
 * Hydrazone iodination
 * Japp–Klingemann reaction
 * Ketone halogenation
 * Koenigs–Knorr reaction
 * Kolbe nitrile synthesis
 * Letts nitrile synthesis
 * Leuckart reaction
 * Malonic ester synthesis
 * McMurry reaction
 * Meerwein arylation
 * Menshutkin reaction
 * Michaelis–Arbuzov reaction
 * Mitsunobu reaction
 * Nef reaction
 * Nicholas reaction
 * Nierenstein reaction
 * Nitration
 * Nucleophilic acyl substitution
 * Nucleophilic aromatic substitution
 * Oxidative decarboxylation
 * Perkow reaction
 * Peterson olefination
 * Prévost reaction
 * Reed reaction
 * Rosenmund–von Braun reaction
 * Ruzicka large-ring synthesis
 * Sandmeyer reaction
 * Saponification
 * Balz–Schiemann reaction
 * Scholl reaction
 * Schotten–Baumann reaction
 * Solvolysis
 * Suzuki reaction
 * Thiolysis
 * Transamidification
 * Transesterification
 * Tsuji–Trost reaction
 * Von Richter reaction
 * Walden inversion
 * Weinreb ketone synthesis
 * Wenker synthesis
 * Williamson ether synthesis
 * Woodward cis-hydroxylation
 * Wurtz–Fittig reaction
 * Zincke nitration
 * Zincke reaction
 * Zincke–Suhl reaction


 * Addition Reactions
 * Addition reaction
 * Electrophilic addition
 * Nucleophilic addition
 * Nucleophilic conjugate addition
 * Syn and anti addition
 * Aldol reaction
 * Aldol–Tishchenko reaction
 * Asymmetric Keck allylation
 * Aza-Baylis–Hillman reaction
 * Barbier reaction
 * Baudisch reaction
 * Baylis–Hillman reaction
 * Betti reaction
 * Bingel reaction
 * Blaise ketone synthesis
 * Blaise reaction
 * Bodroux–Chichibabin aldehyde synthesis
 * Bouveault aldehyde synthesis
 * Cyanohydrin reaction
 * Darzens reaction
 * Duff reaction
 * Ethoxylation
 * Formylation reaction
 * Gattermann reaction
 * Hajos–Parrish–Eder–Sauer–Wiechert reaction
 * Halogen addition reaction
 * Halohydrin formation reaction
 * Hammick reaction
 * Herz reaction
 * Hydration reaction
 * Hydroalkoxylation
 * Hydroamination
 * Hydroboration–oxidation reaction
 * Hydrocyanation
 * Hydrodealkylation
 * Hydroformylation
 * Hydrogenation
 * Hydrohalogenation
 * Ivanov reaction
 * Johnson–Corey–Chaykovsky reaction
 * Julia olefination
 * Kiliani–Fischer synthesis
 * Koch reaction
 * Kolbe–Schmitt reaction
 * Michael reaction
 * Mukaiyama aldol addition
 * Oxymercuration reaction
 * Pinacol coupling reaction
 * Pinner reaction
 * Prins reaction
 * Quelet reaction
 * Reissert reaction
 * Reformatsky reaction
 * Reimer–Tiemann reaction
 * Robinson annulation
 * Rieche formylation
 * Ritter reaction
 * Transalkylation
 * Vilsmeier–Haack reaction
 * Sakurai reaction
 * Simmons–Smith reaction
 * Staudinger synthesis
 * Stetter reaction
 * Yamaguchi esterification
 * Wulff–Dötz reaction


 * Cycloadditions
 * Cycloaddition
 * 1,3-Dipolar cycloaddition
 * Aza-Diels–Alder reaction
 * Azide-alkyne Huisgen cycloaddition
 * Diazoalkane 1,3-dipolar cycloaddition
 * Intramolecular Diels–Alder cycloaddition
 * Inverse electron-demand Diels–Alder reaction
 * 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
 * 2+2 Photocycloaddition


 * Elimination Reactions
 * Elimination reaction
 * 3-aza-Grob fragmentation
 * Bamford–Stevens reaction
 * Chugaev elimination
 * Cope reaction
 * Corey–Winter olefin synthesis
 * Dehydration reaction
 * Dehydrogenation
 * Dehydrohalogenation
 * E1cB-elimination reaction
 * Eschenmoser fragmentation
 * Grieco elimination
 * Grob fragmentation
 * Hofmann elimination
 * Krapcho decarboxylation
 * Ramberg–Bäcklund reaction
 * Varrentrapp reaction


 * Condensation Reactions
 * Condensation reaction
 * Acyloin condensation
 * Aldol condensation
 * Benzoin condensation
 * Biginelli reaction
 * Bucherer–Bergs reaction
 * Claisen condensation
 * Combes quinoline synthesis
 * Conrad–Limpach synthesis
 * Doebner reaction
 * Doebner–Miller reaction
 * Dieckmann condensation
 * Erlenmeyer–Plöchl azlactone and amino-acid synthesis
 * Fischer–Speier esterification
 * Friedländer synthesis
 * Fujimoto–Belleau reaction
 * Guerbet reaction
 * Knoevenagel condensation
 * Madelung synthesis
 * Negishi coupling
 * Niementowski quinazoline synthesis
 * Niementowski quinoline synthesis
 * Pechmann condensation
 * Pellizzari reaction
 * Perkin reaction
 * Pfitzinger reaction
 * Pictet–Spengler reaction
 * Robinson–Gabriel synthesis
 * Self-condensation
 * Skraup reaction
 * Sonogashira coupling
 * Thorpe reaction
 * Ullmann condensation
 * Ullmann reaction
 * Urech hydantoin synthesis
 * Wurtz reaction


 * Degradation Reactions
 * Bergmann degradation
 * Edman degradation
 * Emde degradation
 * Gallagher–Hollander degradation
 * Hooker reaction
 * Marker degradation
 * Strecker degradation
 * Von Braun amide degradation
 * Weerman degradation
 * Wohl degradation


 * Free-Radical Reaction
 * Free-radical reaction
 * Free-radical addition
 * Free-radical halogenation
 * Radical substitution
 * Radical-nucleophilic aromatic substitution
 * Bouveault–Blanc reduction
 * Barton reaction
 * Barton–McCombie deoxygenation
 * Fukuyama indole synthesis
 * Hunsdiecker reaction
 * Kharasch addition
 * Markó–Lam deoxygenation
 * Norrish reaction
 * Wohl–Ziegler bromination


 * Heterocycle Forming Reactions
 * Heterocyclic compound
 * Algar–Flynn–Oyamada reaction
 * Allan–Robinson reaction
 * Auwers synthesis
 * Bamberger triazine synthesis
 * Banert cascade
 * Barton–Zard reaction
 * Bernthsen acridine synthesis
 * Bischler–Napieralski reaction
 * Bucherer carbazole synthesis
 * Chichibabin pyridine synthesis
 * Cook–Heilbron thiazole synthesis
 * Einhorn–Brunner reaction
 * Feist–Benary synthesis
 * Fischer oxazole synthesis
 * Hantzsch pyridine synthesis
 * Knorr pyrrole synthesis
 * Lectka enantioselective beta-lactam synthesis
 * Lehmstedt–Tanasescu reaction
 * Paal–Knorr synthesis
 * Stollé synthesis
 * Wohl–Aue reaction


 * Indole forming reactions
 * Indole
 * Bartoli indole synthesis
 * Bischler–Möhlau indole synthesis
 * Fischer indole synthesis
 * Gassman indole synthesis
 * Hemetsberger indole synthesis
 * Larock indole synthesis
 * Leimgruber–Batcho indole synthesis
 * Martinet dioxindole synthesis
 * Nenitzescu indole synthesis
 * Reissert indole synthesis


 * Quinoline Forming Reactions
 * Quinoline
 * Camps quinoline synthesis
 * Gould–Jacobs reaction
 * Knorr quinoline synthesis


 * Polymerization Reactions
 * Polymerization
 * Addition polymer
 * Chain transfer
 * Acyclic diene metathesis
 * Anionic addition polymerization
 * Atom-transfer radical-polymerization
 * Automatic continuous online monitoring of polymerization reactions
 * Bulk polymerization
 * Cationic polymerization
 * Chain-growth polymerization
 * Chain growth polymerization
 * Cobalt-mediated radical polymerization
 * Condensation polymer
 * Coordination polymerization
 * Degenerative chain transfer
 * Emulsion polymerization
 * Ionic polymerization
 * Living anionic polymerization
 * Living cationic polymerization
 * Living free-radical polymerization
 * Living polymerization
 * Plasma polymerization
 * Precipitation polymerization
 * Radical polymerization
 * Reversible addition−fragmentation chain-transfer polymerization
 * Reversible-deactivation radical polymerization
 * Ring-opening metathesis polymerisation
 * Ring-opening polymerization
 * Solution polymerization
 * Step-growth polymerization
 * Suspension polymerization
 * Ziegler Process


 * Redox Reactions
 * Organic redox reaction
 * Methionine sulfoxide
 * Adkins–Peterson reaction
 * Akabori amino-acid reaction
 * Amide reduction
 * Andrussow process
 * Angeli–Rimini reaction
 * Autoxidation
 * Baeyer–Villiger oxidation
 * Bechamp reduction
 * Benkeser reaction
 * Birch reduction
 * Bosch reaction
 * Boyland–Sims oxidation
 * Cannizzaro reaction
 * Carbonyl oxidation with hypervalent iodine reagents
 * Carbonyl reduction
 * Clemmensen reduction
 * Corey–Itsuno reduction
 * Corey–Kim oxidation
 * Dakin oxidation
 * Deoxygenation
 * Dess-Martin oxidation
 * DNA oxidation
 * Elbs persulfate oxidation
 * Eschweiler–Clarke reaction
 * Étard reaction
 * Fétizon oxidation
 * Fleming–Tamao oxidation
 * Glycol cleavage
 * Grundmann aldehyde synthesis
 * Haloform reaction
 * Hydrogenolysis
 * Hydroxylation
 * Jacobsen epoxidation
 * Jones oxidation
 * Kolbe electrolysis
 * Kornblum oxidation
 * Kornblum–DeLaMare rearrangement
 * Lemieux–Johnson oxidation
 * Ley oxidation
 * Lindgren oxidation
 * Lipid peroxidation
 * Luche reduction
 * McFadyen–Stevens reaction
 * Meerwein–Ponndorf–Verley reduction
 * Microbial arene oxidation
 * Midland Alpine borane reduction
 * Milas hydroxylation
 * Mozingo reduction
 * Nitrile reduction
 * Omega oxidation
 * One-electron reduction
 * Oppenauer oxidation
 * Oxidation of primary alcohols to carboxylic acids
 * Oxidation of secondary alcohols to ketones
 * Oxidation with chromium(VI)-amine complexes
 * Oxoammonium-catalyzed oxidation
 * Parikh–Doering oxidation
 * Pfitzner–Moffatt oxidation
 * Phenol oxidation with hypervalent iodine reagents
 * Pinnick oxidation
 * Reduction of nitro compounds
 * Reductive amination
 * Rosenmund reduction
 * Rubottom oxidation
 * Sabatier reaction
 * Sarett oxidation
 * Selenoxide elimination
 * Shapiro reaction
 * Sharpless asymmetric dihydroxylation
 * Sharpless epoxidation
 * Sharpless oxyamination
 * Shi epoxidation
 * Staudinger reaction
 * Stephen aldehyde synthesis
 * Swern oxidation
 * Transfer hydrogenation
 * Upjohn dihydroxylation
 * Wacker process
 * Wharton reaction
 * Whiting reaction
 * Wolff–Kishner reduction
 * Wolffenstein–Böters reaction
 * Zinin reaction


 * Pericyclic Reactions
 * Pericyclic reaction
 * Cheletropic reaction
 * Electrocyclic reaction
 * Group transfer reaction
 * Stilbene photocyclization


 * Rearrangement Reactions
 * Metal-ion-catalyzed σ-bond rearrangement
 * Rearrangement reaction
 * 1,2-rearrangement
 * 1,2-Wittig rearrangement
 * 2,3-sigmatropic rearrangement
 * Alkyne zipper reaction
 * Allylic rearrangement
 * Alpha-ketol rearrangement
 * Amadori rearrangement
 * Arndt–Eistert reaction
 * Aza-Cope rearrangement
 * Baker–Venkataraman rearrangement
 * Bamberger rearrangement
 * Beckmann rearrangement
 * Benzilic acid rearrangement
 * Bergman cyclization
 * Brook rearrangement
 * Buchner ring expansion
 * Carroll rearrangement
 * Chan rearrangement
 * Claisen rearrangement
 * Cope rearrangement
 * Corey–Fuchs reaction
 * Criegee rearrangement
 * Curtius rearrangement
 * Demjanov rearrangement
 * Di-pi-methane rearrangement
 * Dimroth rearrangement
 * Dowd–Beckwith ring-expansion 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
 * Halogen dance rearrangement
 * Hayashi rearrangement
 * Hofmann rearrangement
 * Hofmann–Martius rearrangement
 * Ireland–Claisen rearrangement
 * Jacobsen rearrangement
 * Kowalski ester homologation
 * Lobry de Bruyn–van Ekenstein transformation
 * Lossen rearrangement
 * McLafferty rearrangement
 * Meyer–Schuster rearrangement
 * Mumm rearrangement
 * Nazarov cyclization reaction
 * Neber rearrangement
 * Newman–Kwart rearrangement
 * Overman rearrangement
 * Piancatelli rearrangement
 * Pinacol rearrangement
 * Pummerer rearrangement
 * Ring expansion and ring 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
 * Tiffeneau–Demjanov rearrangement
 * Vinylcyclopropane rearrangement
 * Wagner–Meerwein rearrangement
 * Wallach rearrangement
 * Westphalen–Lettré rearrangement
 * Willgerodt rearrangement
 * Wolff rearrangement


 * Multiple Component Reactions
 * Multi-component reaction
 * Alkyne trimerisation
 * Asinger reaction
 * Gewald reaction
 * Mannich reaction
 * Passerini reaction
 * Petasis reaction
 * Strecker amino-acid synthesis
 * Ugi reaction


 * Miscellaneous Carbon-Carbon Bond forming Reactions
 * Acetoacetic ester synthesis
 * Alkane metathesis
 * Alkyne metathesis


 * Miscellaneous Carbon-Heteroatom Bond Forming Reactions
 * Boudouard reaction
 * Diazonium compound
 * Grignard reaction