Issue 96, 2012

Iron-mediated direct arylation with arylboronic acids through an aryl radical transfer pathway

Abstract

A novel iron-mediated direct C–H arylation of quinones and pyridine analogues with arylboronic acids has been developed using dichloromethane and water as solvents at ambient temperature. FeS is employed and serves as an efficient catalyst. A detailed reaction mechanism is speculated and expounded.

Graphical abstract: Iron-mediated direct arylation with arylboronic acids through an aryl radical transfer pathway

Supplementary files

Article information

Article type
Communication
Submitted
28 Jul 2012
Accepted
20 Oct 2012
First published
22 Oct 2012

Chem. Commun., 2012,48, 11769-11771

Iron-mediated direct arylation with arylboronic acids through an aryl radical transfer pathway

J. Wang, S. Wang, G. Wang, J. Zhang and X. Yu, Chem. Commun., 2012, 48, 11769 DOI: 10.1039/C2CC35468C

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