Issue 44, 2019

PdCl2(CH3CN)2-catalyzed regioselective C–H olefinations of 2-amino biaryls with vinylsilanes as unactivated alkenes

Abstract

The first example of palladium-catalyzed chelation-assisted C–H olefination of 2-amino biaryls using readily available vinylsilanes as unactivated olefinating reagents has been developed, affording valuable arylated vinylsilane compounds in moderate to excellent yields and with exclusive (E)-selectivities.

Graphical abstract: PdCl2(CH3CN)2-catalyzed regioselective C–H olefinations of 2-amino biaryls with vinylsilanes as unactivated alkenes

Supplementary files

Article information

Article type
Communication
Submitted
20 Mar 2019
Accepted
30 Apr 2019
First published
01 May 2019

Chem. Commun., 2019,55, 6229-6232

PdCl2(CH3CN)2-catalyzed regioselective C–H olefinations of 2-amino biaryls with vinylsilanes as unactivated alkenes

Q. Sun, Z. Li, Z. Xu, Z. Zheng, J. Cao, K. Yang, Y. Cui and L. Xu, Chem. Commun., 2019, 55, 6229 DOI: 10.1039/C9CC02199J

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