Issue 1, 2016

Enantioselective palladium-catalyzed arylation of N-tosylarylimines with arylboronic acids using a chiral 2,2′-bipyridine ligand

Abstract

With the aid of an axially chiral 2,2′-bipyridine ligand, we have successfully developed a palladium-catalyzed method for the enantioselective arylation of N-tosylarylimines, furnishing the chiral diarylmethamines with high yields and enantioselectivities under very mild conditions. An exogenous base was avoided and imine hydrolysis was inhibited in this transformation.

Graphical abstract: Enantioselective palladium-catalyzed arylation of N-tosylarylimines with arylboronic acids using a chiral 2,2′-bipyridine ligand

Supplementary files

Article information

Article type
Communication
Submitted
13 Nov 2015
Accepted
24 Nov 2015
First published
24 Nov 2015

Org. Biomol. Chem., 2016,14, 55-58

Author version available

Enantioselective palladium-catalyzed arylation of N-tosylarylimines with arylboronic acids using a chiral 2,2′-bipyridine ligand

X. Gao, B. Wu, Z. Yan and Y. Zhou, Org. Biomol. Chem., 2016, 14, 55 DOI: 10.1039/C5OB02330K

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