Issue 43, 2016

Transition-metal-free oxidative C5 C–H-halogenation of 8-aminoquinoline amides using sodium halides

Abstract

A simple and efficient transition-metal-free oxidative halogenation (Cl, Br) of the C5 C–H bond of 8-aminoquinoline amides has been developed. This method employed low-cost and innoxious sodium halides as halogenation reagents and oxone as an oxidant. The reactions demonstrated air and moisture tolerance, and good functional group compatibility, giving highly selective C5-halogenated products in good to excellent yields.

Graphical abstract: Transition-metal-free oxidative C5 C–H-halogenation of 8-aminoquinoline amides using sodium halides

Supplementary files

Article information

Article type
Communication
Submitted
22 Sep 2016
Accepted
13 Oct 2016
First published
13 Oct 2016

Org. Biomol. Chem., 2016,14, 10180-10184

Transition-metal-free oxidative C5 C–H-halogenation of 8-aminoquinoline amides using sodium halides

Y. Wang, Y. Wang, K. Jiang, Q. Zhang and D. Li, Org. Biomol. Chem., 2016, 14, 10180 DOI: 10.1039/C6OB02079H

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