Issue 9, 1973

Synthesis and some properties of an oxa-penam

Abstract

Photolysis of N-(ethoxycarbonyl)diazoacetyl-4,4-dimethyloxazolidine (2) gives as major product the oxa-penam ethyl (trans-5H,6H)-2,2-dimethyl-7-oxo-4-oxa-1-azabicyclo[3,2,0]heptane-6-carboxylate (1), the β-lactam function of which is cleaved readily by nucleophilic reagents.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1973, 293-294

Synthesis and some properties of an oxa-penam

B. T. Golding and D. R. Hall, J. Chem. Soc., Chem. Commun., 1973, 293 DOI: 10.1039/C39730000293

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