Issue 8, 2014

Diastereo- and enantioselective reductive amination of cycloaliphatic ketones by preformed chiral palladium complexes

Abstract

An efficient preformed chiral palladium catalyzed direct diastereo- and enantioselective reductive amination of un- and substituted cycloaliphatic ketones with primary aryl amines has been developed.

Graphical abstract: Diastereo- and enantioselective reductive amination of cycloaliphatic ketones by preformed chiral palladium complexes

Supplementary files

Article information

Article type
Paper
Submitted
15 Jan 2014
Accepted
07 Mar 2014
First published
14 Mar 2014

Catal. Sci. Technol., 2014,4, 2626-2630

Author version available

Diastereo- and enantioselective reductive amination of cycloaliphatic ketones by preformed chiral palladium complexes

A. Cabrera, P. Sharma, F. J. Pérez-Flores, L. Velasco, J. L. Arias and L. Rubio-Pérez, Catal. Sci. Technol., 2014, 4, 2626 DOI: 10.1039/C4CY00058G

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