Issue 15, 1969

Preparation of trans-cyclohexane-1,3-diol by the oxymercuration of cyclohex-2-en-1-ol

Abstract

The proportion of cis- and trans-isomers produced in the oxymercuration of cyclohex-2-en-1-ol depends on the conditions for isolation of the product; under acidic conditions, the trans-isomer may be obtained exclusively.

Article information

Article type
Paper

J. Chem. Soc. D, 1969, 866-867

Preparation of trans-cyclohexane-1,3-diol by the oxymercuration of cyclohex-2-en-1-ol

S. Moon, C. Ganz and B. H. Waxman, J. Chem. Soc. D, 1969, 866 DOI: 10.1039/C29690000866

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