Stereoselective Synthesis oftrans-1,2-Di-O-acetyl Glycoses

Abstract
1,2-O-(1-Methoxyethylidene) derivatives of hexopyranoses can be converted to the corresponding trans-1,2-diacetates in a highly stereoselective manner by treatment with trimethylsilyl acetate. O-Acetyl, O-benzyl and O-isopropylidene groups are stable under the reaction conditions.