Issue 10, 1978

Total synthesis of clavulanic acid analogues from 7-oxo-3-vinyl-4-oxa-1-azabicyclo[3.2.0]heptanes

Abstract

A 3-vinyl group has been incorporated into the 7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane ring system by way of the selenoxide elimination process, or by utilising a novel 3-vinylserine derivative, and its transformation to an alkoxyethylidene group demonstrated.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 439-441

Total synthesis of clavulanic acid analogues from 7-oxo-3-vinyl-4-oxa-1-azabicyclo[3.2.0]heptanes

P. H. Bentley and E. Hunt, J. Chem. Soc., Chem. Commun., 1978, 439 DOI: 10.1039/C39780000439

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