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Hosomi-Sakurai reactions of silacyclic allyl silanes
Authors:Sellars Jonathan D  Steel Patrick G  Turner Michael J
Institution:Department of Chemistry, University of Durham, Science Laboratories, South Road, Durham, UK DH1 3LE.
Abstract:Substituted silacyclohexenes, generated through silene-diene 4 + 2] cycloaddition reactions, undergo Lewis acid promoted Sakurai type reactions with acetals to afford, following oxidation of the resultant fluorosilane, 1,4-diols with four contiguous chiral centres.
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