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Highly efficient RuCl3-catalyzed disproportionation of (diacetoxyiodo)benzene to iodylbenzene and iodobenzene; leading to the efficient oxidation of alcohols to carbonyl compounds
Authors:Mekhman S Yusubov  Joo Yeon Park  Viktor V Zhdankin
Institution:a The Siberian State Medical University, 2 Moskovsky trakt, 634050 Tomsk, Russia and The Tomsk Polytechnic University, 30 Lenin st., 634050 Tomsk, Russia
b University of Ulsan, 680-749 Ulsan, Republic of Korea
c Department of Chemistry and Biochemistry, University of Minnesota Duluth, Duluth, Minnesota 55812, USA
Abstract:(Diacetoxyiodo)benzene (DIB) selectively oxidizes primary and secondary alcohols to the respective carbonyl compounds in the presence of RuCl3 (0.8-1.0 mol %) at room temperature in aqueous acetonitrile. This reaction proceeds via an initial instantaneous Ru-catalyzed disproportionation of DIB to iodobenzene and iodylbenzene with the latter acting as the actual stoichiometric oxidant toward alcohols.
Keywords:Hypervalent iodine  (Diacetoxyiodo)benzene  Iodylbenzene  Oxidation  Catalysis
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