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Substituent effects in hydroxyiodination of 1,2-diacyloxycyclohex-3-enes

By J.B. Sweeney, J.R. Knight and S. Thobhani

Abstract

The reaction of 1,2-diacyloxycyclohex-3-enes with iodinating agents in the presence of water has been investigated. The process is inherently diastereoselective, with many reactions giving only two of the four possible diastereoisomers which could be obtained. However, the regiocontrol is variable: highest selectivities are observed when pivalates are present on the periphery of the cycloalkene, when single regio- and diastereoisomers are obtained from the reactions. (c) 2006 Elsevier Ltd. All rights reserved

Year: 2006
DOI identifier: 10.1016/j.tet.2006.08.076
OAI identifier: oai:centaur.reading.ac.uk:11648
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