Literature DB >> 11667872

Synthesis of Novel Chiral Diazole Derivative Ligands for the Enantioselective Addition of Diethylzinc to Benzaldehyde.

Hiyoshizo Kotsuki1, Masahiro Wakao, Hiroyuki Hayakawa, Tomoyasu Shimanouchi, Motoo Shiro.   

Abstract

The high-pressure-promoted reaction of epoxides with pyrazoles and imidazoles provided access to a variety of chiral diazole derivative ligands such as 11-23. Furthermore, chiral pyrazoles 26 and 27, which have a primary alcohol side chain, were also prepared from (+)-camphopyrazole 4. Each of these chiral diazole ligands was used for the catalytic enantioselective addition of diethylzinc to benzaldehyde. The best results were obtained for 16 and 18: 93% ee was achieved in both cases, and reversed asymmetric induction was observed. A plausible mechanism for this efficient asymmetric induction is offered on the basis of X-ray crystallographic data.

Entities:  

Year:  1996        PMID: 11667872     DOI: 10.1021/jo961388c

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Synthesis of substituted pyrazoles via tandem cross-coupling/electrocyclization of enol triflates and diazoacetates.

Authors:  David J Babinski; Hector R Aguilar; Raymond Still; Doug E Frantz
Journal:  J Org Chem       Date:  2011-06-27       Impact factor: 4.354

2.  Imidazole-based potential Bi- and tridentate nitrogen ligands: synthesis, characterization and application in asymmetric catalysis.

Authors:  Roman Sívek; Filip Bures; Oldrich Pytela; Jirí Kulhánek
Journal:  Molecules       Date:  2008-09-25       Impact factor: 4.411

  2 in total

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