Issue 24, 2018

Cp*Rh(iii) catalyzed ortho-halogenation of N-nitrosoanilines by solvent-controlled regioselective C–H functionalization

Abstract

We present a novel, efficient, and regioselective method for the rhodium-catalyzed direct C–H ortho-halogenation of anilines that involves a removable N-nitroso directing group. This method featured mild reaction conditions, wide substrate scope, good functional group tolerance and satisfactory yields. To maintain the high ortho-regioselectivity and conversion, increasing the steric hindrance of the solvent was critical. Preliminary mechanistic studies suggest that C–H activation may be involved in the rate-determining step.

Graphical abstract: Cp*Rh(iii) catalyzed ortho-halogenation of N-nitrosoanilines by solvent-controlled regioselective C–H functionalization

Supplementary files

Article information

Article type
Paper
Submitted
10 Mar 2018
Accepted
25 May 2018
First published
30 May 2018

Org. Biomol. Chem., 2018,16, 4471-4481

Cp*Rh(III) catalyzed ortho-halogenation of N-nitrosoanilines by solvent-controlled regioselective C–H functionalization

Q. Peng, J. Hu, J. Huo, H. Yuan, L. Xu and X. Pan, Org. Biomol. Chem., 2018, 16, 4471 DOI: 10.1039/C8OB00601F

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