Literature DB >> 22322277

A novel C-5' substituted cinchona alkaloid-derived catalyst promotes additions of alkyl thiols to nitroolefins with excellent enantioselectivity.

Carole Palacio1, Stephen J Connon.   

Abstract

A new bifunctional C-5' substituted cinchona alkaloid-based catalyst promotes the first highly enantioselective additions of alkyl thiols to nitrostyrenes.

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Year:  2012        PMID： 22322277     DOI： 10.1039/c2cc17965b

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  4 in total

1.  Enantioselective bifunctional iminophosphorane catalyzed sulfa-Michael addition of alkyl thiols to unactivated β-substituted-α,β-unsaturated esters.

Authors:  Jinchao Yang; Alistair J M Farley; Darren J Dixon
Journal:  Chem Sci       Date:  2016-09-14       Impact factor: 9.825

2.  Bifunctional iminophosphorane catalysed enantioselective sulfa-Michael addition of alkyl thiols to alkenyl benzimidazoles.

Authors:  Michele Formica; Geoffroy Sorin; Alistair J M Farley; Jesús Díaz; Robert S Paton; Darren J Dixon
Journal:  Chem Sci       Date:  2018-07-23       Impact factor: 9.825

3.  Stereoselective Glycosylation of 2-Nitrogalactals Catalyzed by a Bifunctional Organocatalyst.

Authors:  Sandra Medina; Matthew J Harper; Edward I Balmond; Silvia Miranda; Giacomo E M Crisenza; Diane M Coe; Eoghan M McGarrigle; M Carmen Galan
Journal:  Org Lett       Date:  2016-08-16       Impact factor: 6.005

4.  Highly enantioselective sulfa-Michael addition reactions using N-heterocyclic carbene as a non-covalent organocatalyst.

Authors:  Jiean Chen; Sixuan Meng; Leming Wang; Hongmei Tang; Yong Huang
Journal:  Chem Sci       Date:  2015-04-23       Impact factor: 9.825
  4 in total

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