Handbook of reagents for organic synthesis : reagents for heteroarene functionalization / / edited by André B. Charette

• Pubblicazione: West Sussex, England : , : Wiley, , 2015; ©2015
• Descrizione fisica: 1 online resource (829 p.)
• Disciplina: 547/.2
• Soggetto topico: Organic compounds - Synthesis; Heterocyclic chemistry; Chemical tests and reagents
• Persona (resp. second.): CharetteAndré B.
• Note generali: Includes indexes.
• Nota di contenuto: Handbook of Reagents for Organic Synthesis: Reagents for Heteroarene Functionalization; Contents; Preface; Introduction; Recent Review Articles and Monographs; Short Note on InChIs and InChIKeys; Acetic Anhydride; Acetyl Chloride; Aluminum Chloride; Aluminum Trifluoromethanesulfonate; Antimony Trifluoromethanesulfonate; Bathophenanthroline; 1,2-Benzodiazine; Benzopyrazole; Benzotriazole; Bis(allyl)di-μ-chlorodipalladium; Bis(benzonitrile)dichloropalladium(II); Bis(dibenzylideneacetone)palladium(0); Bis(1,10-phenanthroline)palladium Hexafluorophosphate ; Bis[tris(1,1-dimethylethyl)-phosphine]palladiumBromine; N-Bromosuccinimide; n-Butyllithium; sec-Butyllithium; tert-Butyllithium; Butyllithium-Potassium tert-Butoxide; Cesium Acetate; N-Chlorosuccinimide; Copper(II) Acetate; Copper(II) Bromide; Copper(I) Chloride; Copper(II) Chloride; Copper(I) Iodide; Copper(II) Trifluoroacetate; Copper(II) Trifluoromethanesulfonate; N-Cyano-4-methyl-N-phenylbenzenesulfonamide; Dibenzofuran; Dibenzothiophene; 1,1-Di-tert-butyl Peroxide; Di-tert-butyl(methyl)phosphine; Di-tert-butyl(methyl)phosphonium Tetrafluoroborate; Dichlorobis(acetonitrile) Palladium ; Dichlorobis(triphenylphosphine)-palladium(II)Di-μ-chlorotetrakis[(1,2-η)-cyclooctene]diiridium; Di-μ-methoxobis(1,5-cyclooctadiene)diiridium(I); Dimethyl Diazomalonate; (2S,5S)-2-(1,1-Dimethylethyl)-3-methyl-5-(phenylmethyl)-4-imidazolidinone; Diphenyliodonium Hexafluorophosphate; Diphenyliodonium Triflate; Dysprosium Trifluoromethanesulfonate; N-fluoro-N-(phenylsulfonyl)-benzenesulfonamide; 1-Fluoro-2,4,6-trimethylpyridinium Tetrafluoroborate; Furan; Gallium(III) Trifluoromethanesulfonate (Gallium Triflate); Hafnium(IV) Trifluoromethanesulfonate; Hypofluorous Acid-Acetonitrile Complex ; Indium(III) TriflateIndolizine; Iron, Bis(pyridine)bis(2-pyridinecarboxylato-N1,O2); Isoindole; Isoquinoline; Lithium t-Butoxide; Lithium Dichloro(1-methylethyl)-magnesate; Lithium Dichloro(2,2,6,6-tetramethylpiperidinato)-zincate; Magnesium tert-butoxide; Manganese(III) Acetate; 4-Methoxypyridine N-oxide; 6-Methoxyquinoline-N-oxide; 2-Methylbenzothiazole; N-Methylimidazole; N-Methylindole; 1-[[(4-Methylphenyl)sulfonyl]amino]-pyridinium inner salt; Methyltrioxorhenium; Nitric Acid; 4,4,4,́4,́5,5,5,́5-́Octamethyl-2,2-́bi-1,3,2-dioxaborolane; 1,2,5-Oxadiazole; Oxalyl Chloride-Dimethylformamide ; OxazolePalladium(II) Acetate; Palladium(II) Bromide; Palladium(II) Chloride; Palladium(π-cinnamyl) Chloride Dimer; Palladium Pivalate; Pentamethylcyclopentadienylrhodium(III) chloride dimer; 1,10-Phenanthroline; 1,10-Phenanthroline, 1-Oxide; (1,10-Phenanthroline)(trifluoromethyl) (triphenylphosphine)copper; Pinacolborane; Pivalic Acid; Potassium Acetate; Propanoic acid, 2-Diazo-, 2-Methyl-1-(1-methylethyl)propyl ester; Pyridazine; Pyridazine N-Oxide; Pyridine; Pyridine N-Oxide; Pyrrole; Quinoline; Ruthenium Dodecacarbonyltri Triangulo; Scandium Trifluoromethanesulfonate; Silver(I) Acetate ; Silver(I) Carbonate
• Sommario/riassunto: Heteroarenes are among the most prevalent structural units in natural products, pharmaceuticals, agrochemicals, and other compounds of scientific or commercial interest. In the last decade, a broad range of novel synthetic methods has been developed to not only facilitate construction of the heteroarene motif, but to enable its modification through direct C?H functionalization. This Handbook describes 117 key reagents for selective heteroarene functionalization reactions, including both traditional and transition metal-catalyzed C?H functionalization. Since these reactions typically involve o
• Titolo autorizzato: Handbook of reagents for organic synthesis
• ISBN: 1-118-72657-X; 1-118-72655-3
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Lingua di pubblicazione: Inglese
• Record Nr.: 9910810855803321
• Lo trovi qui: Univ. Federico II
• Serie: Hdbk of Reagents for Organic Synthesis