Issue 17, 2015

Rhodium-catalyzed asymmetric addition of arylboronic acids to cyclic N-sulfonyl ketimines towards the synthesis of α,α-diaryl-α-amino acid derivatives

Abstract

Rhodium/chiral diene complex-catalyzed asymmetric addition of arylboronic acids to cyclic ketimines having an ester group proceeded to give the corresponding α-amino acid derivatives in high yields with high enantioselectivity. The cyclic amino acid derivative was transformed into a linear α,α-diaryl-substituted α-N-methylamino acid ester.

Graphical abstract: Rhodium-catalyzed asymmetric addition of arylboronic acids to cyclic N-sulfonyl ketimines towards the synthesis of α,α-diaryl-α-amino acid derivatives

Supplementary files

Article information

Article type
Paper
Submitted
04 Mar 2015
Accepted
17 Mar 2015
First published
18 Mar 2015
This article is Open Access
Creative Commons BY license

Org. Biomol. Chem., 2015,13, 4918-4924

Author version available

Rhodium-catalyzed asymmetric addition of arylboronic acids to cyclic N-sulfonyl ketimines towards the synthesis of α,α-diaryl-α-amino acid derivatives

R. Takechi and T. Nishimura, Org. Biomol. Chem., 2015, 13, 4918 DOI: 10.1039/C5OB00431D

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