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Flavin-cyclodextrin catalysts

More recently, Kraus has reported the use of flavin-cyclodextrin conjugate catalyst 41 for the asymmetric oxidation of both aromatic and aliphatic methyl thioethers, using hydrogen peroxides in a phosphate buffer (Scheme 19.19) [120, 121]. [Pg.539]

Scheme 19.19 Oxidation of thioethers with flavin-cyclodextrin catalyst 4V... Scheme 19.19 Oxidation of thioethers with flavin-cyclodextrin catalyst 4V...
The hydrogen peroxide-mediated oxidation of p-tolyl methyl sulfide with chiral iminium salt 20 (Figure 19.9), reported in 1993, gives a 32% ee [81]. The use of chiral flavinium salt catalysts afforded a 65% ee for the same transformation [119], More recently, Kraus has reported the use of flavin-cyclodextrin conjugate catalyst 41 for the asymmetric oxidation of both aromatic and aliphatic methyl thioethers, using hydrogen peroxides in a phosphate buffer (Scheme 19.19) [120, 121]. [Pg.539]


See other pages where Flavin-cyclodextrin catalysts is mentioned: [Pg.1408]    [Pg.161]    [Pg.154]    [Pg.328]    [Pg.346]    [Pg.103]    [Pg.125]    [Pg.112]    [Pg.328]   
See also in sourсe #XX -- [ Pg.540 ]




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