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ChemInform 2008, 39, issue 49 ©WlLEY-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Oxidation O 0212 Highly Efficient Oxidation of Alcohols Using Oxone® as Oxidant Catalyzed by Ruthenium Complex under Mild Reaction Conditions. — Benzyl alcohols (I) are oxidized to the corresponding aldehydes; benzhydrols (III) and cycloalkanols (VI) are converted to ketones. The oxidation of aliphatic alcohols (VII) is possible, but a mixture of aldehydes and carboxylic acids is formed. — (LEI*, Z. Q.; WANG, J. Q.; YAN, P. H.; Chin. Chem. Lett. 19 (2008) 9, 1031-1034; State Key Lab. Polym. Mater., Coll. Chem. Chem. Eng., Northwest Norm. Univ., Lanzhou, Gansu 730070, Peop. Rep. China; Eng.) — R. Simon 49- 034

ChemInform Abstract: Highly Efficient Oxidation of Alcohols Using Oxone® as Oxidant Catalyzed by Ruthenium Complex under Mild Reaction Conditions

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OxidationO 0212 Highly Efficient Oxidation of Alcohols Using Oxone® as Oxidant Catalyzed by

Ruthenium Complex under Mild Reaction Conditions. — Benzyl alcohols (I) are oxidized to the corresponding aldehydes; benzhydrols (III) and cycloalkanols (VI) are converted to ketones. The oxidation of aliphatic alcohols (VII) is possible, but a mixture of aldehydes and carboxylic acids is formed. — (LEI*, Z. Q.; WANG, J. Q.; YAN, P. H.; Chin. Chem. Lett. 19 (2008) 9, 1031-1034; State Key Lab. Polym. Mater., Coll. Chem. Chem. Eng., Northwest Norm. Univ., Lanzhou, Gansu 730070, Peop. Rep. China; Eng.) — R. Simon

49- 034

ChemInform 2008, 39, issue 49 ©WlLEY-VCH Verlag GmbH & Co. KGaA, Weinheim