Issue 18, 1986

The first biomimetic conversion of a germacrolide-4-epoxide into a xanthanolide

Abstract

Boron trifluoride catalysed cyclization of the germacrolide-4-epoxide dihydroparthenolide (1) provided two known guaianolides and the xanthanolide (4), the latter transformation representing the first biomimetic conversion of a germacrolide into a xanthanolide.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 1405-1405

The first biomimetic conversion of a germacrolide-4-epoxide into a xanthanolide

F. J. Parodi and N. H. Fischer, J. Chem. Soc., Chem. Commun., 1986, 1405 DOI: 10.1039/C39860001405

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