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