HYDROXYHALOGENATIONS OF ACYLOXYCYCLOHEX-2-ENES - PART-3 - ITERATIVE 1,2-HYDROXYIODINATION OF ACETOXYCYCLOHEX-2-ENE - PREPARATION OF TETRAACETYL CONDURITOL-D

Citation
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
Citations number
16
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
0300922X
Issue
6
Year of publication
1998
Pages
1039 - 1046
Database
ISI
SICI code
0300-922X(1998):6<1039:HOA-P->2.0.ZU;2-#
Abstract
Compound 22, the tetraacetyl derivative of conduritol D, has been synt hesized by repeated hydroxyiodination reactions in nine steps from ace toxycyclohex-2-ene.