oaioai:centaur.reading.ac.uk:11648

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

Authors
Publication date
1 January 2006
Publisher
Doi

    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

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      Central Archive at the University of Reading

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      Last time updated on 04/04/2012

      This paper was published in Central Archive at the University of Reading.

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