Chemical Communications

Highly diastereoselective hydrosilylations of allylic alcohols

MG McLaughlin, MJ Cook

Index: McLaughlin, Mark G.; Cook, Matthew J. Chemical Communications, 2014 ,  vol. 50,  # 26  p. 3501 - 3504

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Citation Number: 5

Abstract

The highly syn-selective hydrosilylation of allylic alcohols was developed which, following oxidation, provided 1, 3 alcohols containing two contiguous stereocentres. Through judicious choice of silane the complementary anti-selective hydrosilylation was also developed. This protocol was applied to the synthesis of an all syn polyketide stereotriad.