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RECENT ADVANCES IN THE SYNTHESIS OF SULFOXIDES FROM SULFIDES

Article

Date
1996
Publishing House and Editing Place
TAYLOR & FRANCIS LTD
Magazine
PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS, vol. 117 (pp. 231-286) TAYLOR & FRANCIS LTD
Summary Information provided by the agent in SIGEVA
This review deals with the various recent advances in the selective oxidation of sulfides to sulfoxides. Non-stereoselective, diastereoselective as well as enantioselective methods are covered. A considerable number of new oxidizing agents have been reported in the last ten to twelve years including those aiming to replace m-chloroperbenzoic acid as the classical sulfide oxidant: Oxone" dimethyldioxirane, among others. Chiral sulfoxides are especially important in modem asymmetric synthesi... This review deals with the various recent advances in the selective oxidation of sulfides to sulfoxides. Non-stereoselective, diastereoselective as well as enantioselective methods are covered. A considerable number of new oxidizing agents have been reported in the last ten to twelve years including those aiming to replace m-chloroperbenzoic acid as the classical sulfide oxidant: Oxone" dimethyldioxirane, among others. Chiral sulfoxides are especially important in modem asymmetric synthesis. their obtention from prochiral sulfides by Davis' oxaziridines and modifications of Sharpless procedure are discussed, along with other less common methods. The most newly reported microbiological and enzymatic oxidations are also included.
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Key Words
sulfoxidesoxidation