Issue 8, 1988
From the journal:

Journal of the Chemical Society, Chemical Communications

Novel construction of penems and carbapenems. Further evidence of a carbene intermediate for the oxalimide cyclization reaction

Tetsuji Kametani,   Shih-Der Chu,   Akira Itoh,   Tzu-Chueh Wang,   Atsushi Nakayama  and  Toshio Honda  

Abstract

A novel construction of penem and carbapenem ring systems has been achieved by employing an oxalimide cyclization as a key step.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/C39880000544
Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 544-546

Permissions

Request permissions

Novel construction of penems and carbapenems. Further evidence of a carbene intermediate for the oxalimide cyclization reaction

T. Kametani, S. Chu, A. Itoh, T. Wang, A. Nakayama and T. Honda, J. Chem. Soc., Chem. Commun., 1988, 544 DOI: 10.1039/C39880000544

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