Issue 7, 1993

General synthesis of inositols by hydrolysis of conduritol epoxides obtained biocatalytically from halogenobenzenes: (+)-D-chiro-inositol, allo-inositol, muco-inositol and neo-inositol

Abstract

Four of the nine isomeric inositols have been prepared by hydrolytic opening of epoxides derived from 3-halogenocyclohexa-3,5-diene-1,2-diol by further oxidation with potassium permanganate or by reduction of chiro-3-inosose (2L-2,3,6/4,5-pentahydroxycyclohexanone).

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1993, 741-743

General synthesis of inositols by hydrolysis of conduritol epoxides obtained biocatalytically from halogenobenzenes: (+)-D-chiro-inositol, allo-inositol, muco-inositol and neo-inositol

M. Mandel and T. Hudlicky, J. Chem. Soc., Perkin Trans. 1, 1993, 741 DOI: 10.1039/P19930000741

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