Issue 47, 2019, Issue in Progress

Metal-free oxidative cross-dehydrogenative coupling of quinones with benzylic C(sp3)–H bonds

Abstract

A metal-free cross-dehydrogenative coupling of quinones with toluene derivatives has been established. A series of quinones were subjected to reaction with toluene derivatives in the presence of di-tertbutyl peroxide (DTBP) for direct synthesis of benzylquinones. The method exhibits good functional group tolerance, and desired products were obtained in moderate to good yields. Meanwhile, a radical pathway was proposed to describe the cross-dehydrogenative coupling of quinones with toluene derivatives.

Graphical abstract: Metal-free oxidative cross-dehydrogenative coupling of quinones with benzylic C(sp3)–H bonds

Supplementary files

Article information

Article type
Paper
Submitted
23 Jul 2019
Accepted
28 Aug 2019
First published
02 Sep 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 27588-27592

Metal-free oxidative cross-dehydrogenative coupling of quinones with benzylic C(sp3)–H bonds

Y. Dong, J. Yang, S. He, Z. Shi, Y. Wang, X. Zhang and J. Wang, RSC Adv., 2019, 9, 27588 DOI: 10.1039/C9RA05678E

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