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Dinuclear peroxotungstate

The highly chemo-, regio-, and diastereoselective and stereospecific epoxidation of various allylic alcohols with only 1 equivalent of hydrogen peroxide in water solvent could be efficiently catalyzed by an isolated dinuclear peroxotungstate [W203(02)4(H20)2]2 [93,94] ... [Pg.474]

K. Kamata, K. Yamaguchi, N. Mizuno, Highly selective, recyclable epoxidation of allylic alcohols with hydrogen peroxide in water catalyzed by dinuclear peroxotungstate, Chem. Eur. J. 10 (2004) 4728. [Pg.173]

K. Kamata, S. Kuzuya, K. Uehara, S. Yamaguchi, N. Mizuno, p-q q -Peroxo-bridged dinuclear peroxotungstate catalytically active for epoxidation of olefins, Inorg. Chem. 46 (2007) 3768. [Pg.173]

See other pages where Dinuclear peroxotungstate is mentioned: [Pg.410]    [Pg.410]    [Pg.168]    [Pg.169]    [Pg.190]    [Pg.942]    [Pg.159]    [Pg.166]    [Pg.168]    [Pg.169]    [Pg.190]    [Pg.140]    [Pg.146]    [Pg.1232]    [Pg.410]    [Pg.410]    [Pg.168]    [Pg.169]    [Pg.190]    [Pg.942]    [Pg.159]    [Pg.166]    [Pg.168]    [Pg.169]    [Pg.190]    [Pg.140]    [Pg.146]    [Pg.1232]    [Pg.159]   
See also in sourсe #XX -- [ Pg.159 ]



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