Issue 0, 1973

Synthetic studies on terpenoids. Part XVI. Synthesis of 3β,17-diacetoxyphyllocladen-15-one

Abstract

A stereoselective synthesis of 3β,17-diacetoxyphyllocladen-15-one (XIX) from ethyl 5,5-ethylenedioxy-2-oxo-cyclohexanecarboxylate proceeding in ten stages via methyl 13,13-ethylenedioxy-3-oxopodocarpa-5,9(11)-diene-8β-carboxylate (V) and methyl 3β-hydroxy-13-oxopodocarpane-8β-carboxylate (XII) is described. The ester (XII) has been correlated with a known degradation product from phyllocladene. Some by-products from the hydrogenation of the diene (V) are discussed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1973, 2083-2088

Synthetic studies on terpenoids. Part XVI. Synthesis of 3β,17-diacetoxyphyllocladen-15-one

D. Mukherjee, S. K. Mukhopadhyay, K. K. Mahalanabis, A. D. Gupta and P. C. Dutta, J. Chem. Soc., Perkin Trans. 1, 1973, 2083 DOI: 10.1039/P19730002083

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