Issue 71, 2019

The Ag-promoted α-C–H arylation of alcohols

Abstract

We herein report the functionalization of α-C–H in alcohols through cross-dehydrogenative coupling reactions. Selectfluor was used as a mild oxidant. In situ-generated HF participated in the reaction and no external strong acid was necessary. A variety of heteroaryl-substituted alcohols were achieved with good yields and with good functional group tolerance.

Graphical abstract: The Ag-promoted α-C–H arylation of alcohols

Supplementary files

Article information

Article type
Paper
Submitted
22 Nov 2019
Accepted
02 Dec 2019
First published
17 Dec 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 41847-41850

The Ag-promoted α-C–H arylation of alcohols

S. Wang, S. Xing, Y. Zhang, Y. Fan, H. Zhao, J. Wang, S. Zhang and W. Wang, RSC Adv., 2019, 9, 41847 DOI: 10.1039/C9RA09954A

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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