HYDROXYHALOGENATIONS OF ACYLOXYCYCLOHEX-2-ENES - PART-3 - ITERATIVE 1,2-HYDROXYIODINATION OF ACETOXYCYCLOHEX-2-ENE - PREPARATION OF TETRAACETYL CONDURITOL-D
J. Bange et al., HYDROXYHALOGENATIONS OF ACYLOXYCYCLOHEX-2-ENES - PART-3 - ITERATIVE 1,2-HYDROXYIODINATION OF ACETOXYCYCLOHEX-2-ENE - PREPARATION OF TETRAACETYL CONDURITOL-D, Journal of the Chemical Society. Perkin transactions. I, (6), 1998, pp. 1039-1046
Compound 22, the tetraacetyl derivative of conduritol D, has been synt
hesized by repeated hydroxyiodination reactions in nine steps from ace
toxycyclohex-2-ene.