Issue 18, 1983

Stereoselective synthesis of a (5R,6S)-6-[(R)-1-hydroxyethyl]-2-thioxo-penam ester through a hydroxy group directed chlorinolysis

Abstract

Hydroxy group directed chlorinolysis of (3S,4R)-3-[(R)-1-hydroxyethyl]-4-ethylthioazetidin-2-one (4) gives predominantly the corresponding (4S)-4-chloroazetidinone (5) which is cyclised to the (5R,6S)-6[(R)-1-hydroxyethyl]-2-thioxopenam (1).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 1006-1007

Stereoselective synthesis of a (5R,6S)-6-[(R)-1-hydroxyethyl]-2-thioxo-penam ester through a hydroxy group directed chlorinolysis

N. Daniels, G. Johnson and B. C. Ross, J. Chem. Soc., Chem. Commun., 1983, 1006 DOI: 10.1039/C39830001006

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