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

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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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Official URL: http://dx.doi.org/10.1039/a709056k

DOI: 10.1039/a709056k

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
Related URLs:	Author
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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