期刊
ORGANIC LETTERS
卷 10, 期 18, 页码 4041-4044出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol801574m
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资金
- Dutch Ministry of Economic Affairs
- Spanish Ministry of Education and Science
The catalytic enantioselective Reformatsky reaction with ortho-substituted diarylketones with good enantioselectivities and moderate to good yields is reported. A readily available BINOL derivative is used as a chiral catalyst, and the reactions are performed with ethyl iodoacetate as a nucleophile and Me2Zn as the zinc source. The presence of air was found to be crucial to achieve an effective C-C bond formation pointing to a radical mechanism.
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