Issue 33, 2017, Issue in Progress
From the journal:

RSC Advances

Copper-catalyzed C–C direct cross-coupling: an efficient approach to phenyl-2-(phenylthiophenyl)-methanones†

Qi Zhang,a   Wei Wang,a   Chong Gao,a   Rong-Rong Caia  and  Run-Sheng Xu ORCID logo *a  

* Corresponding authors

a Department of Biology and Environment, Jiyang College of Zhejiang A&F University, Hangzhou 311800, Zhejiang, China
E-mail: 20140041@zafu.edu.cn

Abstract

An efficient copper-catalyzed C–C bond direct cross-coupling reaction has been developed. Starting from diaryl sulfoxides and aromatic aldehydes, versatile phenyl-2-(phenylthiophenyl)-methanones were efficiently synthesized with high tolerance of functional groups under moderate conditions in water. This new methodology provides an economical and environmentally friendly approach toward C(sp2)–C(sp2) bond formation.

Graphical abstract: Copper-catalyzed C–C direct cross-coupling: an efficient approach to phenyl-2-(phenylthiophenyl)-methanones

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Article information

DOI
https://doi.org/10.1039/C7RA01403A
Article type
Paper
Submitted
03 Feb 2017
Accepted
23 Mar 2017
First published
06 Apr 2017
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2017,7, 20123-20127

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Copper-catalyzed C–C direct cross-coupling: an efficient approach to phenyl-2-(phenylthiophenyl)-methanones

Q. Zhang, W. Wang, C. Gao, R. Cai and R. Xu, RSC Adv., 2017, 7, 20123 DOI: 10.1039/C7RA01403A

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