Issue 9, 1984

Preparation of bicyclic lactones: precursors for the synthesis of paniculides B and C

Abstract

A stereoselective approach to the paniculide skeleton is reported utilizing an approach based on the dilithioacetate opening of an epoxide and demonstrating the high degree of regio-and stereo-control possible in this reaction, epoxidation, reduction and phenylselenation reactions.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 619-621

Preparation of bicyclic lactones: precursors for the synthesis of paniculides B and C

R. Baker, C. L. Gibson, C. J. Swain and D. J. Tapolczay, J. Chem. Soc., Chem. Commun., 1984, 619 DOI: 10.1039/C39840000619

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