Role of Hexafluoro-2-propanol in Selective Oxidation of Sulfide to Sulfoxide: Efficient Preparation of Glycosyl Sulfoxides

K.S. Ravikumar(Centre National de la Recherche Scientifique), Yongmin Zhang(École Normale Supérieure - PSL), Jean‐Pierre Bégué, Danièle Bonnet‐Delpon(Centre National de la Recherche Scientifique)
European Journal of Organic Chemistry
December 1, 1998
Cited by 94

Abstract

Aqueous 30% H2O2 in hexafluoro-2-propanol (HFIP) is described as a facile, selective and efficient oxidant for the conversion of sulfides to sulfoxides under neutral conditions. The nitrogen center of the pyridine molecule and the carbon–carbon double bond are shown to not be affected by the reagent system used. The oxidation of glycosyl sulfides to glycosyl sulfoxides was achieved in very high yield at room temperature.


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