Issue 2, 1985

Highly stereoselective preparation of enantiomerically pure 1,2-diols: synthesis of (+)-exobrevicomin

Abstract

Reduction of optically pure acyl-lactones (2) by L-Selectride affords monoprotected syn diols with high diastereoselectivity; the reaction was applied to the stereo- and enantio-specific synthesis of (+)-exobrevicomin.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 83-84

Highly stereoselective preparation of enantiomerically pure 1,2-diols: synthesis of (+)-exobrevicomin

M. Larchevêque and J. Lalande, J. Chem. Soc., Chem. Commun., 1985, 83 DOI: 10.1039/C39850000083

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