Literature DB >> 10836024

Enantioselective ring opening of meso aziridines catalyzed by Tridentate Schiff base chromium(III) complexes.

Z Li1, M Fernández, E N Jacobsen.   

Abstract

[formula: see text] A catalytic method for the enantioselective ring opening of meso aziridines by TMSN3 is described. Tridentate Schiff base chromium complexes derived from 1-amino-2-indanol were identified as the optimal catalysts.

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Year:  1999        PMID： 10836024     DOI： 10.1021/ol990992h

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  4 in total

1.  Bifunctional Asymmetric Catalysis with Hydrogen Chloride: Enantioselective Ring-Opening of Aziridines Catalyzed by a Phosphinothiourea.

Authors:  Tsuyoshi Mita; Eric N Jacobsen
Journal:  Synlett       Date:  2009-06-01       Impact factor: 2.454

2.  Chiral phosphoric acid-catalyzed desymmetrization of meso-aziridines with functionalized mercaptans.

Authors:  Shawn E Larson; Juan C Baso; Guilong Li; Jon C Antilla
Journal:  Org Lett       Date:  2009-11-19       Impact factor: 6.005

3.  Aziridines as intermediates in diversity-oriented syntheses of alkaloids.

Authors:  Alexander M Taylor; Stuart L Schreiber
Journal:  Tetrahedron Lett       Date:  2009-07-02       Impact factor: 2.415

Review 4.  Organocatalyzed enantioselective desymmetrization of aziridines and epoxides.

Authors:  Ping-An Wang
Journal:  Beilstein J Org Chem       Date:  2013-08-15       Impact factor: 2.883
  4 in total

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