Issue 20, 1979

The ent-neo-clerodane absolute configuration of ajugarins

Abstract

The absolute configurations of the caryoptins and ajugarins are enantiomeric and both should be reversed from those previously proposed; the absolute configuration of the caryoptins can be correctly derived from the dibenzoate chirality method.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1979, 885-886

The ent-neo-clerodane absolute configuration of ajugarins

G. Trivedi, H. Komura, I. Kubo, K. Nakanishi and B. S. Joshi, J. Chem. Soc., Chem. Commun., 1979, 885 DOI: 10.1039/C39790000885

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