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Hydroxyhalogenations of acyloxycyclohex-2-enes. Part 3.1 Iterative 1,2-hydroxyiodination of acetoxycyclohex-2-ene: preparation of tetraacetyl conduritol D

Bange, Johannes, Haughan, Alan F., Knight, J. R. and Sweeney, Joseph B. (1998) Hydroxyhalogenations of acyloxycyclohex-2-enes. Part 3.1 Iterative 1,2-hydroxyiodination of acetoxycyclohex-2-ene: preparation of tetraacetyl conduritol D. Journal of the Chemical Society, Perkin Transactions 1 (6). pp. 1039-1046. ISSN 0300-922X

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Abstract

Compound 22, the tetraacetyl derivative of conduritol D, has been synthesized by repeated hydroxyiodination reactions in nine steps from acetoxycyclohex-2-ene.

Item Type: Article
Subjects: Q Science > QD Chemistry
Schools: School of Applied Sciences
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Depositing User: Joseph Sweeney
Date Deposited: 18 Oct 2012 11:09
Last Modified: 18 Oct 2012 11:09
URI: http://eprints.hud.ac.uk/id/eprint/15389

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