Issue 1, 1971

Partial synthesis of mexicanolide from 7-oxo-7-deacetoxykhivorin

Abstract

7-Oxo-7-deacetoxykhivorin has been transformed into the diene-lactone (XI), a postulated biogenetic precursor of the bicyclonanolide group of tetranortriterpenoids, which when treated with very mild base readily undergoes intramolecular Michael addition to give mexicanolide (XII).

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 17-18

Partial synthesis of mexicanolide from 7-oxo-7-deacetoxykhivorin

J. D. Connolly, I. M. S. Thornton and D. A. H. Taylor, J. Chem. Soc. D, 1971, 17 DOI: 10.1039/C29710000017

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