Literature DB >> 19109665

Asymmetric reduction of ketimines with trichlorosilane employing an imidazole derived organocatalyst.

François-Moana Gautier1, Simon Jones, Stephen J Martin.   

Abstract

Organocatalysts for the asymmetric reduction of ketimines are presented that function well at low catalyst loadings providing chiral amines in good yield and enantioselectivity, the latter appearing to be independent of the ketimine substrate geometry.

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Year:  2008        PMID： 19109665     DOI： 10.1039/b816051a

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


  3 in total

1.  Enantioselective reduction of ketoimines promoted by easily available (S)-proline derivatives.

Authors:  Martina Bonsignore; Maurizio Benaglia; Laura Raimondi; Manuel Orlandi; Giuseppe Celentano
Journal:  Beilstein J Org Chem       Date:  2013-04-02       Impact factor: 2.883

2.  Chiral aminophosphines as catalysts for enantioselective double-Michael indoline syntheses.

Authors:  San N Khong; Ohyun Kwon
Journal:  Molecules       Date:  2012-05-11       Impact factor: 4.411

3.  Regioselective Mercury(I)/Palladium(II)-Catalyzed Single-Step Approach for the Synthesis of Imines and 2-Substituted Indoles.

Authors:  Rsuini U Gutiérrez; Mayra Hernández-Montes; Aarón Mendieta-Moctezuma; Francisco Delgado; Joaquín Tamariz
Journal:  Molecules       Date:  2021-07-05       Impact factor: 4.411
  3 in total

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