期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 132, 期 14, 页码 4986-+出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja100748y
关键词
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资金
- NIGMS [R01 01 GM093213-01]
- Natural Sciences and Engineering Research Council (NSERC)
An enantioselective organocatalytic alpha-trifluoromethylation of aldehydes has been accomplished using a commercially available, electrophilic trifluoromethyl source. The merging of Lewis acid and organocatalysis provides a new strategy for the enantioselective construction of trifluoromethyl stereogenicity, an important chiral synthon for pharmaceutical, materials, and agrochemical applications. This mild and operationally simple protocol allows rapid access to enantioenriched alpha-trifluoromethylated aldehydes through a nonphotolytic pathway.
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