User:Drpundir/Books/Named Organic Chemistry
 | The Wikimedia Foundation's book rendering service has been withdrawn. Please upload your Wikipedia book to one of the external rendering services. |
 | You can still create and edit a book design using the Book Creator and upload it to an external rendering service:
|
| This user book is a user-generated collection of Wikipedia articles that can be easily saved, rendered electronically, and ordered as a printed book. If you are the creator of this book and need help, see Help:Books (general tips) and WikiProject Wikipedia-Books (questions and assistance). Edit this book: Book Creator · Wikitext Order a printed copy from: PediaPress [ About ] [ Advanced ] [ FAQ ] [ Feedback ] [ Help ] [ WikiProject ] [ Recent Changes ] | ||||||||
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