Issue 4, 1994

Carbon–carbon bond formation at the C-4 position of an azetidin-2-one ring by intermolecular radical coupling reactions: a route to tribactams

Abstract

The β-lactam 4 was linked to the enones 810 using a radical reaction mediated by tri-n-butyltin hydride to give the 2,6-disubstituted cyclohexanones 1116, respectively: 13 was converted into the protected tribactam 18 in two steps.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 441-442

Carbon–carbon bond formation at the C-4 position of an azetidin-2-one ring by intermolecular radical coupling reactions: a route to tribactams

A. Padova, S. M. Roberts, D. Donati, A. Perboni and T. Rossi, J. Chem. Soc., Chem. Commun., 1994, 441 DOI: 10.1039/C39940000441

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