Literature DB >> 29711328

Catalytic, Enantioselective Synthesis of α-Aminonitriles with a Novel Zirconium Catalyst.

Haruro Ishitani1, Susumu Komiyama1, Shū Kobayashi1.   

Abstract

Strecker reactions of aldimines with Bu3 SnCN in the presence of the novel chiral zirconium binuclear catalyst 1 provide α-aminonitriles in good yields and with high enantioselectivities. The reaction can be applied to a wide range of substrates. Since both enantiomers of the chiral sources are readily avaibable, both enantiomers of the α-aminonitriles are easily prepared according to this method. L=N-methylimidazole. © 1998 WILEY-VCH Verlag GmbH, Weinheim, Fed. Rep. of Germany.

Entities:  

Keywords:  Amino acids; Asymmetric catalysis; Asymmetric synthesis; Lewis acids; Zirconium

Year:  1998        PMID: 29711328     DOI: 10.1002/(SICI)1521-3773(19981204)37:22<3186::AID-ANIE3186>3.0.CO;2-E

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  1 in total

1.  Stereoselective synthesis of novel 2'-(S)-CCG-IV analogues as potent NMDA receptor agonists.

Authors:  Alex Maolanon; Athanasios Papangelis; David Kawiecki; Tung-Chung Mou; Jed T Syrenne; Feng Yi; Kasper B Hansen; Rasmus P Clausen
Journal:  Eur J Med Chem       Date:  2020-12-18       Impact factor: 6.514

  1 in total

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