Issue 44, 2016

A new cost-effective Ru-chloramphenicol base derivative catalyst for the asymmetric transfer hydrogenation/dynamic kinetic resolution of N-Boc α-amino-β-ketoesters and its application to the synthesis of the chiral core of vancomycin

Abstract

Herein we describe the application of a series of newly developed Ru-chloramphenicol base derivative complexes as catalysts for the highly diastereo- and enantioselective transfer hydrogenation of N-Boc α-amino-β-ketoesters for the asymmetric synthesis of anti-N-Boc-β-hydroxy-α-amino esters. This report highlights the utility of this catalytic methodology for the preparation of pharmaceutical compounds bearing a N-Boc α-amino-β-hydroxy substructure with two stereocenters.

Graphical abstract: A new cost-effective Ru-chloramphenicol base derivative catalyst for the asymmetric transfer hydrogenation/dynamic kinetic resolution of N-Boc α-amino-β-ketoesters and its application to the synthesis of the chiral core of vancomycin

Supplementary files

Article information

Article type
Paper
Submitted
26 Feb 2016
Accepted
10 Apr 2016
First published
11 Apr 2016

RSC Adv., 2016,6, 37701-37709

A new cost-effective Ru-chloramphenicol base derivative catalyst for the asymmetric transfer hydrogenation/dynamic kinetic resolution of N-Boc α-amino-β-ketoesters and its application to the synthesis of the chiral core of vancomycin

X. Wang, L. Xu, F. Xiong, Y. Wu and F. Chen, RSC Adv., 2016, 6, 37701 DOI: 10.1039/C6RA05109J

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