Issue 0, 1972

Synthesis of primulagenin A and of echinocystic acid

Abstract

Photolysis of 3β-acetoxyolean-12-en-28-amide with lead tetra-acetate and iodine gave, albeit in low yield, the corresponding 28,15β-lactone. Further transformations of the latter then afforded primulagenin A (olean-12-ene-3β,16α,28-triol), which can be converted into echinocystic acid (3β,16α-dihydroxyolean-12-en-28-oic acid).

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1972, 2994-3001

Synthesis of primulagenin A and of echinocystic acid

J. Allen, R. B. Boar, J. F. McGhie and D. H. R. Barton, J. Chem. Soc., Perkin Trans. 1, 1972, 2994 DOI: 10.1039/P19720002994

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements