Literature DB >> 18080260

Organocatalytic enantioselective one-pot synthesis and application of substituted 1,4-dihydropyridines--Hhantzsch ester analogues.

Patrick T Franke1, Rasmus L Johansen, Søren Bertelsen, Karl Anker Jørgensen.   

Abstract

An easy and simple one-pot approach for the formation of optically active substituted 1,4-dihydropyridines by using asymmetric organocatalysis is presented. The one-pot reaction of alpha,beta-unsaturated aldehydes with beta-diketones or beta-ketoesters and primary amines gives optically active 2,3-substituted 1,4-dihydropyridines in moderate yields and with enantioselectivities up to 95 % ee. It is also demonstrated that the optically active 1,4-dihydropyridines can be used in situ for the direct enantioselective reduction of, for example, alpha-ketoesters with high enantioselectivity.

Entities:  

Year:  2008        PMID: 18080260     DOI: 10.1002/asia.200700360

Source DB:  PubMed          Journal:  Chem Asian J        ISSN: 1861-471X


  2 in total

1.  Enantioselective organocatalytic Hantzsch synthesis of polyhydroquinolines.

Authors:  Christopher G Evans; Jason E Gestwicki
Journal:  Org Lett       Date:  2009-07-16       Impact factor: 6.005

2.  Diethyl 4-(2-meth-oxy-phen-yl)-2,6-di-methyl-1,4-di-hydro-pyridine-3,5-di-carboxyl-ate.

Authors:  Ke Wang; Yifeng Wang; Minjie Yao; Danqian Xu
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-04-24
  2 in total

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