Wednesday, January 27, 2016

Rhodium(III)-Catalyzed Coupling of Arenes with Cyclopropanols via C–H Activation and Ring Opening

http://pubs.acs.org/doi/abs/10.1021/acscatal.5b02414

Rhodium(III)-Catalyzed Coupling of Arenes with Cyclopropanols via C–H Activation and Ring Opening

Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China
ACS Catal., 2016, 6, pp 647–651
DOI: 10.1021/acscatal.5b02414
Publication Date (Web): December 21, 2015
Copyright © 2015 American Chemical Society
OpenURL UNIV OF VIRGINIA
*E-mail: xwli@dicp.ac.cn.

Abstract

Abstract Image
Rhodium-catalyzed C–H activation of arenes has been established as an important strategy for the rapid construction of new bonds. On the other hand, ring-opening of readily available cyclopropanols has served as a driving force for the coupling with various nucleophiles and electrophiles. Nevertheless, these two important areas evolved separately, and coupling of arenes with cyclopropanols via C–H activation has been rarely explored. In this work, the oxidative coupling between arenes and cyclopropanols has been realized with high efficiency and selectivity under Rh(III)-catalysis, providing an efficient route to access β-aryl ketones. Moreover, the C–H bond has been extended to benzylic C–H bonds.

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