Literature DB >> 18219416

Enantioselective addition of nitromethane to alpha-keto esters catalyzed by copper(II)-iminopyridine complexes.

Gonzalo Blay1, Victor Hernández-Olmos, José R Pedro.   

Abstract

The copper complex of a chiral iminopyridine easily prepared from (R)-(-)-fenchone and picolylamine catalyzes the enantioselective Henry (nitroaldol) reaction between nitromethane and alpha-keto esters. Good yields and modest to good enantioselectivities are obtained for a wide range of alpha-keto esters, bearing aromatic, alkyl or alkenyl groups attached to the ketone carbonyl group.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 18219416     DOI: 10.1039/b716446g

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  Dynamic kinetic asymmetric transformations of β-stereogenic α-ketoesters by direct aldolization.

Authors:  Michael T Corbett; Jeffrey S Johnson
Journal:  Angew Chem Int Ed Engl       Date:  2013-11-12       Impact factor: 15.336

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

Authors:  Feilong He; Guanghui Chen; Junxia Yang; Guojuan Liang; Ping Deng; Yan Xiong; Hui Zhou
Journal:  RSC Adv       Date:  2018-03-05       Impact factor: 4.036

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.