User:Drpundir/Books/Named Organic Chemistry

Named Organic Chemistry

 * 1,2-rearrangement
 * 1,2-Wittig rearrangement
 * 1,3-Dipolar cycloaddition
 * 2+2 Photocycloaddition
 * 2,3-sigmatropic rearrangement
 * Acetoacetic ester synthesis
 * Acetylation
 * Achmatowicz reaction
 * Acyclic diene metathesis
 * Acylation
 * Acyloin condensation
 * Adamkeiwickz reaction
 * Adams decarboxylation
 * Addition polymer
 * Addition reaction
 * Adkins–Peterson reaction
 * Akabori amino-acid reaction
 * Alcohol oxidation
 * Alder ene reaction
 * Aldol reaction
 * Aldol-Tishchenko reaction
 * Algar–Flynn–Oyamada reaction
 * Alkylation
 * Alkylimino-de-oxo-bisubstitution
 * Alkyne trimerisation
 * Alkyne zipper reaction
 * Allan–Robinson reaction
 * Allylic rearrangement
 * Allylic stannane addition
 * Alpha cleavage
 * Alpha-ketol rearrangement
 * Amadori rearrangement
 * Amide reduction
 * Amination
 * Amine alkylation
 * Aminoacylation
 * Aminolysis
 * Andrussow process
 * Angeli–Rimini reaction
 * Anionic addition polymerization
 * Annulation
 * Appel reaction
 * Armed and disarmed saccharides
 * Arndt–Eistert reaction
 * Aromatic sulfonation
 * Asinger reaction
 * Associative substitution
 * Asymmetric ester hydrolysis with pig-liver esterase
 * Asymmetric nucleophilic epoxidation
 * Atom-transfer radical-polymerization
 * Automatic continuous online monitoring of polymerization reactions
 * Autoxidation
 * Auwers synthesis
 * Aza-Baylis–Hillman reaction
 * Aza-Diels–Alder reaction
 * Azide-alkyne Huisgen cycloaddition
 * Azo coupling
 * Baeyer–Drewson indigo synthesis
 * Baeyer–Emmerling indole synthesis
 * Baeyer–Villiger oxidation
 * Baker–Venkataraman rearrangement
 * Balz–Schiemann reaction
 * Bamberger rearrangement
 * Bamberger triazine synthesis
 * Bamford–Stevens reaction
 * Banert cascade
 * Barbier reaction
 * Bardhan-Senguph phenanthrene synthesis
 * Bartoli indole synthesis
 * Barton decarboxylation
 * Barton reaction
 * Barton vinyl iodine procedure
 * Barton–Kellogg reaction
 * Barton–McCombie deoxygenation
 * Barton–Zard synthesis
 * Base-promoted epoxide isomerization
 * Baudisch reaction
 * Baylis–Hillman reaction
 * Bechamp reaction
 * Bechamp reduction
 * Beckmann rearrangement
 * Belousov–Zhabotinsky reaction
 * Benary reaction
 * Benkeser reaction
 * Benzilic acid rearrangement
 * Benzylic activation and stereocontrol in tricarbonyl(arene)chromium complexes
 * Bergman cyclization
 * Bergmann azlactone peptide synthesis
 * Bergmann degradation
 * Bernthsen acridine synthesis
 * Betti reaction
 * Biginelli reaction
 * Bingel reaction
 * Birch reduction
 * Birkeland–Eyde process
 * Bischler–Möhlau indole synthesis
 * Bischler–Napieralski reaction
 * Blaise ketone synthesis
 * Blaise reaction
 * Blanc chloromethylation
 * Bodroux reaction
 * Bodroux–Chichibabin aldehyde synthesis
 * Bohn-Schmidt reaction
 * Boord olefin synthesis
 * Borodin reaction
 * Borsche-Drechsel cyclization
 * Bosch reaction
 * Boudouard reaction
 * Bouveault aldehyde synthesis
 * Bouveault–Blanc reduction
 * Boyland–Sims oxidation
 * Bray–Liebhafsky reaction
 * Briggs–Rauscher reaction
 * Brook rearrangement
 * Bucherer carbazole synthesis
 * Bucherer reaction
 * Bucherer–Bergs reaction
 * Buchner ring expansion
 * Buchwald–Hartwig amination
 * Cadiot–Chodkiewicz coupling
 * Camps quinoline synthesis
 * Cannizzaro reaction
 * Carbene C−H insertion
 * Carbene dimerization
 * Carbohydrate acetalisation
 * Carbohydrate synthesis
 * Carbometalation
 * Carbonyl Alpha-Substitution Reactions
 * Carbonyl oxidation with hypervalent iodine reagents
 * Carbonyl reduction
 * Carboxylation
 * Carbylamine reaction
 * Carroll rearrangement
 * Castro–Stephens coupling
 * Chan rearrangement
 * Chapman rearrangement
 * Cheletropic reaction
 * Chichibabin pyridine synthesis
 * Chichibabin reaction
 * Chugaev elimination
 * Claisen condensation
 * Claisen rearrangement
 * Clemmensen reduction
 * Coal liquefaction
 * Combes quinoline synthesis
 * Concerted reaction
 * Condensation reaction
 * Conrad–Limpach synthesis
 * Cook–Heilbron thiazole synthesis
 * Cope reaction
 * Cope rearrangement
 * Copper-free click chemistry
 * Corey–Fuchs reaction
 * Corey–House synthesis
 * Corey–Itsuno reduction
 * Corey–Kim oxidation
 * Corey–Winter olefin synthesis
 * Cracking (chemistry)
 * Crich beta-mannosylation
 * Criegee rearrangement
 * Cumene process
 * Curtius rearrangement
 * Cyanohydrin reaction
 * Cycloaddition
 * Dakin oxidation
 * Dakin–West reaction
 * Danheiser annulation
 * Darzens reaction
 * Deamidation
 * Deamination
 * Debus-Radziszewski imidazole synthesis
 * Decarboxylation
 * Delépine reaction
 * DeMayo reaction
 * Demethylation
 * Demjanov rearrangement
 * Deoxygenation
 * Dess-Martin oxidation
 * Dess–Martin periodinane
 * Destructive distillation
 * Desulfonylation reactions
 * Di-pi-methane rearrangement
 * Diazoalkane 1,3-dipolar cycloaddition
 * Diels Reese reaction
 * Diels–Alder reaction
 * Dimroth rearrangement
 * Directed ortho metalation
 * Disproportionation
 * Divinylcyclopropane-cycloheptadiene rearrangement
 * DNA oxidation
 * Doebner reaction
 * Doebner–Miller reaction
 * Dowd–Beckwith ring-expansion reaction
 * Doyle–Kirmse reaction
 * Dry distillation
 * Duff reaction
 * Dyotropic reaction
 * Edman degradation
 * Einhorn–Brunner reaction
 * Elaidinization
 * Elbs persulfate oxidation
 * Elbs reaction
 * Electrocyclic reaction
 * Electrophilic addition
 * Electrophilic amination
 * Electrophilic aromatic substitution
 * Electrophilic fluorination
 * Electrophilic halogenation
 * Electrophilic substitution
 * Electrophilic substitution of unsaturated silanes
 * Emde degradation
 * Enantioselective reduction of ketones
 * Enders SAMP/RAMP hydrazone-alkylation reaction
 * Epoxidation with dioxiranes
 * Erlenmeyer–Plöchl azlactone and amino-acid synthesis
 * Eschenmoser fragmentation
 * Eschenmoser sulfide contraction
 * Eschweiler–Clarke reaction
 * Ester pyrolysis
 * Ethoxylation
 * Evans–Saksena reduction
 * Favorskii reaction
 * Favorskii rearrangement
 * Feist–Benary synthesis
 * Ferrier carbocyclization
 * Ferrier rearrangement
 * Finkelstein reaction
 * Fischer glycosidation
 * Fischer indole synthesis
 * Fischer oxazole synthesis
 * Fischer–Hepp rearrangement
 * Fischer–Speier esterification
 * Fleming–Tamao oxidation
 * Fluorination by sulfur tetrafluoride
 * Fluorination with aminosulfuranes
 * Formose reaction
 * Formylation reaction
 * Forster–Decker method
 * Free-radical addition
 * Freund reaction
 * Friedel–Crafts reaction
 * Friedländer synthesis
 * Fries rearrangement
 * Fritsch–Buttenberg–Wiechell rearrangement
 * Fráter–Seebach alkylation
 * Fujimoto–Belleau reaction
 * Fukuyama coupling
 * Fukuyama indole synthesis
 * Fukuyama reduction
 * Gabriel synthesis
 * Gabriel–Colman rearrangement
 * Gallagher–Hollander degradation
 * Gasification
 * Gasifier Experimenters Kit
 * Gassman indole synthesis
 * Gattermann reaction
 * Gattermann–Koch reaction
 * Geminal halide hydrolysis
 * Gewald reaction
 * Girdler sulfide process
 * Glycol cleavage
 * Glycosyl acceptor
 * Glycosyl donor
 * Glycosylation
 * Goldberg reaction
 * Gomberg–Bachmann reaction
 * Gould–Jacobs reaction
 * Grieco elimination
 * Grignard reaction
 * Grob fragmentation
 * Grundmann aldehyde synthesis
 * Guerbet reaction
 * Haber–Weiss reaction
 * Hajos–Parrish–Eder–Sauer–Wiechert reaction
 * Haller-Bauer reaction
 * Haloform reaction
 * Halogen addition reaction
 * Halogenation
 * Halohydrin formation reaction
 * Hammick reaction
 * Hantzsch pyridine synthesis
 * Hantzsch pyrrole synthesis
 * Hayashi rearrangement
 * Heck reaction
 * Heck–Matsuda reaction
 * Helferich method
 * Hell–Volhard–Zelinsky halogenation
 * Herz reaction
 * Heteroatom-promoted lateral lithiation
 * Histone acetylation and deacetylation
 * Hoesch reaction
 * Hofmann–Löffler reaction
 * Hooker reaction
 * Hydration reaction
 * Hydrazone iodination
 * Hydroacylation
 * Hydroamination
 * Hydroboration
 * Hydroboration–oxidation reaction
 * Hydrocyanation
 * Hydrodealkylation
 * Hydroformylation
 * Hydrogenation
 * Hydrogenation of carbon–nitrogen double bonds
 * Hydrogenolysis
 * Hydrohalogenation
 * Hydrous pyrolysis
 * Hydroxylation
 * Imine Diels–Alder reaction
 * Inductive cleavage
 * Intermolecular metal-catalyzed carbenoid cyclopropanations
 * Intramolecular Diels–Alder cycloaddition
 * Intramolecular Heck reaction
 * Intramolecular reactions of diazocarbonyl compounds
 * Inverse electron-demand Diels–Alder reaction
 * Iodolactonization
 * Ivanov reaction
 * Jacobsen epoxidation
 * Japp–Klingemann reaction
 * Johnson–Corey–Chaykovsky reaction
 * Jones oxidation
 * Julia olefination
 * Keto-enol tautomerism
 * Ketone halogenation
 * Ketonic decarboxylation
 * Kharasch addition
 * Kiliani–Fischer synthesis
 * Koch reaction
 * Kochi reaction
 * Koenigs–Knorr reaction
 * Kolbe electrolysis
 * Kolbe nitrile synthesis
 * Kolbe–Schmitt reaction
 * Kornblum oxidation
 * Kornblum–DeLaMare rearrangement
 * Kostanecki acylation
 * Krapcho decarboxylation
 * Leaving group
 * Lemieux–Johnson oxidation
 * Letts nitrile synthesis
 * Leuckart reaction
 * Leuckart thiophenol reaction
 * Ley oxidation
 * Lindgren oxidation
 * Lipid peroxidation
 * Liquid-feed flame spray pyrolysis
 * List of organic reactions
 * Luche reduction
 * Lumière–Barbier method
 * Malonic ester synthesis
 * Manganese-mediated coupling reactions
 * Mannich reaction
 * Markó–Lam deoxygenation
 * Marschalk reaction
 * McCormack reaction
 * McFadyen–Stevens reaction
 * McMurry reaction
 * Meerwein arylation
 * Meerwein–Ponndorf–Verley reduction
 * Menshutkin reaction
 * Metal-ion-catalyzed σ-bond rearrangement
 * Methanation
 * Methionine sulfoxide
 * Methylation
 * Meyers synthesis
 * Michael reaction
 * Michaelis–Arbuzov reaction
 * Michaelis–Becker reaction
 * Microbial arene oxidation
 * Minisci reaction
 * Mitsunobu reaction
 * Mukaiyama aldol addition
 * Multi-component reaction
 * Name reaction
 * Nef reaction
 * Nicholas reaction
 * Nierenstein reaction
 * Nitration
 * Nitrone-olefin 3+2 cycloaddition
 * Nitrosation
 * Nucleophilic acyl substitution
 * Nucleophilic addition
 * Nucleophilic aromatic substitution
 * Nucleophilic conjugate addition
 * Nucleophilic substitution
 * Organic reaction
 * Organic redox reaction
 * Organostannane addition
 * Oxidation with chromium(VI)-amine complexes
 * Oxidation with dioxiranes
 * Oxidative decarboxylation
 * Oxo-Diels–Alder reaction
 * Oxocarbenium
 * Oxymercuration reaction
 * Ozonolysis
 * Passerini reaction
 * Paternò–Büchi reaction
 * Pauson–Khand reaction
 * Payne rearrangement
 * Pericyclic reaction
 * Perkow reaction
 * Petasis reaction
 * Peterson olefination
 * Photooxygenation
 * Pinacol coupling reaction
 * Pinner reaction
 * Pinner triazine synthesis
 * Polymerization
 * Povarov reaction
 * Prato reaction
 * Prins reaction
 * Prévost reaction
 * Pyrolysis
 * Pyrolysis oil
 * Quelet reaction
 * Radical cyclization
 * Reactions of alkenyl- and alkynylaluminium compounds
 * Reactions of organoborates and boranes
 * Reactions of organocopper reagents
 * Rearrangement reaction
 * Reductions with diimide
 * Reductions with hydrosilanes
 * Reductions with metal alkoxyaluminium hydrides
 * Reductions with samarium(II) iodide
 * Reductive dehalogenation of halo ketones
 * Reed reaction
 * Reformatsky reaction
 * Reichstein process
 * Reimer–Tiemann reaction
 * Reissert reaction
 * Retro-Diels–Alder reaction
 * Rieche formylation
 * Riemschneider thiocarbamate synthesis
 * Ritter reaction
 * Robinson annulation
 * Rosenmund–von Braun reaction
 * Ruzicka large-ring synthesis
 * Sakurai reaction
 * Sandmeyer reaction
 * Saponification
 * Scholl reaction
 * Schotten–Baumann reaction
 * Schöllkopf method
 * Simmons–Smith reaction
 * SN1 reaction
 * Sn1CB mechanism
 * SN2 reaction
 * SNi
 * Soai reaction
 * Solvolysis
 * Sommelet reaction
 * Staudinger synthesis
 * Stereochemistry of ketonization of enols and enolates
 * Stetter reaction
 * Stilbene photocyclization
 * Strecker amino-acid synthesis
 * Strecker degradation
 * Substitution reaction
 * Suzuki reaction
 * Syn and anti addition
 * Synthesis of 2-amino-2-deoxysugars
 * Synthesis of nucleosides
 * Takai olefination
 * Thermal depolymerization
 * Thiol-yne reaction
 * Thiolysis
 * Tipson–Cohen reaction
 * Tishchenko reaction
 * Torrefaction
 * Transalkylation
 * Transamidification
 * Transamination
 * Transesterification
 * Transmethylation
 * Trifluoromethylation
 * Trimethylenemethane cycloaddition
 * Tsuji–Trost reaction
 * Ugi reaction
 * Vicarious nucleophilic substitution
 * Vicinal difunctionalization
 * Vilsmeier–Haack reaction
 * Volhard–Erdmann cyclization
 * Von Braun reaction
 * Von Richter reaction
 * Wagner-Jauregg reaction
 * Walden inversion
 * Weinreb ketone synthesis
 * Wenker synthesis
 * Williamson ether synthesis
 * Wohl–Ziegler bromination
 * Wood gas
 * Wood gas generator
 * Woodward cis-hydroxylation
 * Wulff–Dötz reaction
 * Wurtz–Fittig reaction
 * Wöhler synthesis
 * Zincke nitration
 * Zincke reaction
 * Zincke–Suhl reaction
 * Étard reaction