Issue 11, 1991

Partial synthesis of some diterpenoids with potential antitumour activity

Abstract

The diterpenoid fungal metabolite, fujenal, has been converted into analogues of the Rabdosia diterpenoids, ent-7-hydroxy-15-oxo-6,7-secokaur-16-en-6,19-dioic acid 6,7-lactone 19-methyl ester and ent-7-acetoxy-19-hydroxy-15-oxo-6,7-secokaur-16-en-6-oic acid 6,19-lactone which possess moderate inhibitory activity against HeLa cells.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1991, 2679-2682

Partial synthesis of some diterpenoids with potential antitumour activity

M. S. Ali, M. K. Baynham, J. R. Hanson and P. B. Hitchcock, J. Chem. Soc., Perkin Trans. 1, 1991, 2679 DOI: 10.1039/P19910002679

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