Issue 21, 1988

The synthesis of the δ-lactone portion of the mevinic acids; a new non-acidic method of cyclic lactone expansion

Abstract

An alkoxy-mercuration demercuration sequence has been used as the key step in an enantiospecific synthesis of a protected synthon for the lactone porton of the mevinic acids.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 1417-1418

The synthesis of the δ-lactone portion of the mevinic acids; a new non-acidic method of cyclic lactone expansion

A. H. Davidson, C. D. Floyd, C. N. Lewis and P. L. Myers, J. Chem. Soc., Chem. Commun., 1988, 1417 DOI: 10.1039/C39880001417

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