Issue 17, 2018, Issue in Progress

Catalytic enantioselective Henry reaction of α-keto esters, 2-acylpyridines and 2-acylpyridine N-oxides

Abstract

A pre-prepared Ni–PyBisulidine complex has been developed for the catalytic asymmetric Henry reaction of α-keto esters, 2-acylpyridines and 2-acylpyridine N-oxides. The corresponding β-nitro-α-hydroxy esters were obtained in good to excellent yields (up to 99%) with a high enantiomeric excess (ee) (up to 94%) with a catalyst loading of 1–2 mol%. The desired products of 2-acylpyridines and 2-acylpyridine N-oxides, which were simple methyl ketones, were obtained in medium to excellent yields (up to 94%) with medium to good ee (up to 86%) by using 2 mol% of catalyst.

Graphical abstract: Catalytic enantioselective Henry reaction of α-keto esters, 2-acylpyridines and 2-acylpyridine N-oxides

Supplementary files

Article information

Article type
Paper
Submitted
19 Jan 2018
Accepted
19 Feb 2018
First published
05 Mar 2018
This article is Open Access
Creative Commons BY license

RSC Adv., 2018,8, 9414-9422

Catalytic enantioselective Henry reaction of α-keto esters, 2-acylpyridines and 2-acylpyridine N-oxides

F. He, G. Chen, J. Yang, G. Liang, P. Deng, Y. Xiong and H. Zhou, RSC Adv., 2018, 8, 9414 DOI: 10.1039/C8RA00552D

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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