期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 132, 期 9, 页码 2860-+出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja910281s
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- Eli Lilly
Asymmetric hydration of alpha,alpha-dichloro aldehydes and alpha-halo enals via a NHC-catalyzed redox process to yield enantioenriched alpha-chloro and alpha-fluoro carboxylic acids is described herein. The developed reaction allows for installation of an alpha-deuterium to give rise to enantioenriched alpha-deutero alpha-halo acids Using D2O as the deuteron source.
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