Issue 29, 2015

Passerini/Tsuji–Trost strategies towards achieving lactams and cyclopentane derivatives

Abstract

The Passerini reaction of α,β-unsaturated aldehydes affords suitable substrates for the Tsuji–Trost reaction with various carbon based-nucleophiles. The resulting α,β-unsaturated amides may be cyclized to lactams or converted into cyclopentane derivatives if bis-nucleophiles are used in the Tsuji–Trost step.

Graphical abstract: Passerini/Tsuji–Trost strategies towards achieving lactams and cyclopentane derivatives

Supplementary files

Article information

Article type
Communication
Submitted
21 Jan 2015
Accepted
19 Feb 2015
First published
19 Feb 2015

Chem. Commun., 2015,51, 6411-6414

Author version available

Passerini/Tsuji–Trost strategies towards achieving lactams and cyclopentane derivatives

M. Cordier, A. Dos Santos, L. El Kaïm and N. Narboni, Chem. Commun., 2015, 51, 6411 DOI: 10.1039/C5CC00584A

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