期刊
CHEMICAL COMMUNICATIONS
卷 55, 期 27, 页码 3923-3926出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cc01159e
关键词
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资金
- JSPS KAKENHI [18K05123]
- Sumitomo Foundation
- Okayama Foundation for Science and Technology
- Grants-in-Aid for Scientific Research [18K05123] Funding Source: KAKEN
A catalytic enantioselective Hosomi-Sakurai reaction of -ketoesters has been developed. A copper(ii) complex with a chiral bis(oxazoline) ligand bearing methanesulfonamide groups shows excellent catalytic activity to give ,-disubstituted -hydroxyesters in high yields with high enantioselectivities. This is the first successful method for the catalytic enantioselective 1,2-addition of -ketoesters with allylic silanes.
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