Issue 6, 1981
From the journal:

Journal of the Chemical Society, Chemical Communications

2H n.m.r. determination of the stereochemistry of an allylic displacement in the biosynthesis of virescenol B

David E. Cane,   Heinz Hasler,   Joan Materna,   Nera Cagnoli-Bellavita,   Paolo Ceccherelli,   Gian Federico Madruzza  and  Judith Polonsky  

Abstract

Feeding of (5R)-[5-2H]mevalonate to Oospora virescens and 2H n.m.r. analysis of a derivative of the resulting virescenol B establish that the allylic displacement of pyrophosphate which generates ring c takes place with overall anti stereochemistry.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/C39810000280
Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 280-282

Permissions

Request permissions

2 H n.m.r. determination of the stereochemistry of an allylic displacement in the biosynthesis of virescenol B

D. E. Cane, H. Hasler, J. Materna, N. Cagnoli-Bellavita, P. Ceccherelli, G. F. Madruzza and J. Polonsky, J. Chem. Soc., Chem. Commun., 1981, 280 DOI: 10.1039/C39810000280

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