Issue 0, 1980

The chemistry of 4-mercaptoazetidin-2-ones. Part 2. Synthesis of bisnorpenicillins

Abstract

Reaction of the 4-mercaptoazetidinone (2) with benzyl 2-bromoacrylate gave the C-3-epimeric bisnorpenicillin esters (6b) and (7b). Standard procedures were used to convert the ester (6b) into bisnorpenicillin V (3) and bisnorampicillin (15). By contrast (2), with either (E)- or (Z)-benzyl 2-bromocrotonates, gave the penam esters (20) and (21) and not the expected benzyl esters of the norpenicillanic acids (16a) and (16b). This reaction was shown to proceed via the olefin (22).

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1980, 150-155

The chemistry of 4-mercaptoazetidin-2-ones. Part 2. Synthesis of bisnorpenicillins

N. F. Osborne, J. Chem. Soc., Perkin Trans. 1, 1980, 150 DOI: 10.1039/P19800000150

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