Issue 13, 1995

Efficient access to the ‘Ziegler intermediate’ in the total synthesis of forskolin

Abstract

Lactone 3, easily prepared from hydroxy-β-ionone, is transformed into the Ziegler intermediate in forskolin synthesis by a straightforward strategy involving two new rearrangements.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 1333-1334

Efficient access to the ‘Ziegler intermediate’ in the total synthesis of forskolin

M. Leclaire, F. Pericaud and J. Y. Lallemand, J. Chem. Soc., Chem. Commun., 1995, 1333 DOI: 10.1039/C39950001333

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