Issue 89, 2016, Issue in Progress

Carbonylative coupling of aryl tosylates/triflates with arylboronic acids under CO atmosphere

Abstract

The carbonylative Suzuki–Miyaura reaction between aryl tosylates/triflates with arylboronic acid is herein reported, using base-free conditions and a balloon pressure of carbon monoxide. Under these conditions, unsymmetrical biaryl ketones were obtained in modest to excellent yields. This method was adapted to the synthesis of oxybenzone and ketoprofen in good yields under mild conditions.

Graphical abstract: Carbonylative coupling of aryl tosylates/triflates with arylboronic acids under CO atmosphere

Supplementary files

Article information

Article type
Paper
Submitted
06 Jun 2016
Accepted
02 Sep 2016
First published
12 Sep 2016

RSC Adv., 2016,6, 86502-86509

Carbonylative coupling of aryl tosylates/triflates with arylboronic acids under CO atmosphere

C. Y. Hao, D. Wang, Y. W. Li, L. L. Dong, Y. Jin, X. R. Zhang, H. Y. Zhu and S. Chang, RSC Adv., 2016, 6, 86502 DOI: 10.1039/C6RA14678C

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