Issue 16, 1999

Unexpected formation of β-lactams and penem isosteres from mesoionics: sequential ring-opening–rearrangement of [3 + 2] cycloadducts

Abstract

A novel and simple method has been developed to obtain penem analogs with biologically interesting functionalities, which combines aromatic aldehydes with thioisomünchnones, a readily available class of mesoionic heterocycles.

Supplementary files

Article information

Article type
Paper

Chem. Commun., 1999, 1589-1590

Unexpected formation of β-lactams and penem isosteres from mesoionics: sequential ring-opening–rearrangement of [3 + 2] cycloadducts

M. Avalos, R. Babiano, P. Cintas, J. L. Jiménez, I. López, J. C. Palacios, M. B. Hursthouse and M. E. Light, Chem. Commun., 1999, 1589 DOI: 10.1039/A904333K

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.

Social activity

Spotlight

Advertisements