Issue 15, 1999

Asymmetric synthesis of the core cyclopentane of viridenomycin

Abstract

The fully substituted cyclopentene ring with three stereogenic centers has been efficiently constructed for the first time using chiral bicyclic lactams, the insertion of the quaternary center being the key step; ring opening of chiral sulfates to the correct 1,2-dihydroxy substituents also played a major role in reaching 1 in suitable form (18) for further study.

Article information

Article type
Paper

Chem. Commun., 1999, 1371-1372

Asymmetric synthesis of the core cyclopentane of viridenomycin

M. P. Arrington and A. I. Meyers, Chem. Commun., 1999, 1371 DOI: 10.1039/A903160J

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.

Social activity

Spotlight

Advertisements