A practical, efficient method for preparation of four possible stereoisomers of secondary allylic alcohols using kinetic resolution of (E)-1-trimethylsilylalk-1-en-3-ol by the sharpless process

Abstract
Kinetic resolution of (E)-1-trimethylsilylalk-1-en-3-ol by the Sharpless process, which proceeds with very large rate differences for the two isomers, combined with the reactivity of epoxysilyl compounds affords a practical, efficient method for preparation of four possible stereoisomers of secondary allylic alcohols.
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