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Oral Contributions

Highly Enantioselective Oxidation of Aryl Benzyl Sulfides

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Pages 1193-1195 | Received 08 Sep 2010, Accepted 30 Sep 2010, Published online: 12 Jul 2011
 

Abstract

Enantiopure aryl benzyl sulfoxides were easily obtained by an enantioselective oxidation of the corresponding sulfides with tert-butyl hydroperoxide in the presence of a complex between titanium and (S, S)- or (R, R)-hydrobenzoin. Theoretical and experimental investigations confirmed that these aryl benzyl sulfides represent an ideal substrate for the asymmetric oxidation system.

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