Issue 52, 2013

Palladium-catalysed aerobic oxidative Heck-type alkenylation of Csp3–H for pyrrole synthesis

Abstract

The first palladium-catalysed aerobic oxidative intramolecular alkenylation of Csp3–H bonds was described. The reaction conditions were mild and molecular oxygen was used as the terminal oxidant. Kinetic studies showed that the Csp3–H metallation step was a slow step.

Graphical abstract: Palladium-catalysed aerobic oxidative Heck-type alkenylation of Csp3–H for pyrrole synthesis

Supplementary files

Article information

Article type
Communication
Submitted
29 Mar 2013
Accepted
07 May 2013
First published
09 May 2013

Chem. Commun., 2013,49, 5853-5855

Palladium-catalysed aerobic oxidative Heck-type alkenylation of Csp3–H for pyrrole synthesis

L. Meng, K. Wu, C. Liu and A. Lei, Chem. Commun., 2013, 49, 5853 DOI: 10.1039/C3CC42307G

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