Literature DB >> 18604828

Chiral Schiff bases as highly active and enantioselective catalysts in catalytic addition of dialkylzinc to aldehydes.

Takanori Tanaka1, Yuki Sano, Masahiko Hayashi.   

Abstract

We have developed chiral Schiff base catalysts based on the ONO-tridentate ligand for the catalytic enantioselective addition of dialkylzinc to aldehydes. Various aldehydes were smoothly converted into corresponding optically active secondary alcohols with high enantioselectivity (up to 98 % ee) in high yield. Furthermore, we have succeeded in decreasing the catalyst loading minimum to 0.1 mol % in the chiral Schiff base-catalyzed enantioselective alkylation of aldehydes.

Entities:  

Year:  2008        PMID: 18604828     DOI: 10.1002/asia.200800132

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


  1 in total

Review 1.  Synthesis of heteroaromatic compounds by oxidative aromatization using an activated carbon/molecular oxygen system.

Authors:  Yuka Kawashita; Masahiko Hayashi
Journal:  Molecules       Date:  2009-08-14       Impact factor: 4.411

  1 in total

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