期刊
CHEMICAL COMMUNICATIONS
卷 46, 期 6, 页码 904-906出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/b919929b
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资金
- U.S. National Institutes of Health [R01GM069990]
- NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM069990, R56GM069990] Funding Source: NIH RePORTER
Hydrogen bond catalyzed Mukaiyama aldol reactions of alpha-ketoesters proceed in high diastereo- and enantioselectivities, giving products possessing two chiral centers, of which one is a tertiary alcohol.
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