Silylene acetals from cheap reagents: synthesis and regioselective opening

Abstract

In this communication, a practical method for using cheap and easily available silylene chlorides for diol protection is presented. The method is based on activation of the reagents using Finkelstein-like conditions. Silylene acetals of carbohydrates are synthesized, and it is furthermore shown how these can be regioselectively opened using Grignard reagents.