Issue 6, 1998

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

Abstract

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

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1998, 1039-1046

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

J. Bange, A. F. Haughan, J. R. Knight and J. Sweeney, J. Chem. Soc., Perkin Trans. 1, 1998, 1039 DOI: 10.1039/A709056K

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