Issue 0, 1984

Rearrangement of rosifoliol epoxides: transformation of eudesmane to valencane sesquiterpene types

Abstract

A study has been made of the rearrangement of derivatives of the eudesmane sesquiterpene, (+)-rosifoliol (3), to valencane structures. This biogenetically significant methyl migration has been accomplished via Lewis acid-catalysed epoxide opening.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1984, 1323-1328

Rearrangement of rosifoliol epoxides: transformation of eudesmane to valencane sesquiterpene types

R. Ramage and I. A. Southwell, J. Chem. Soc., Perkin Trans. 1, 1984, 1323 DOI: 10.1039/P19840001323

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