期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 139, 期 25, 页码 8428-8431出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.7b04816
关键词
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资金
- Novartis International AG
- National Institutes of Health [GM58160]
- National Science Foundation [CHE-0946721]
This report details a general and enantioselective means for the synthesis of alkyl-substituted aziridines. This protocol offers a direct route for the synthesis of alkyl-substituted chiral aziridines from achiral starting materials. Readily accessed allylic hydroxylamine esters undergo copper hydride-catalyzed intramolecular hydroamination with a high degree of regio- and enantiocontrol to afford the aziridine products in good to excellent yields in highly enantioenriched form. The utility of the products derived from this method is further demonstrated through derivatization of the chiral aziridine products to obtain a diverse array of functionalized enantioenriched amines.
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