User:Drpundir/Books/Named Organic Chemistry

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Named Organic Chemistry[edit]

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