| Literature DB >> 11667872 |
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