期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 132, 期 39, 页码 13633-13635出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja105442m
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资金
- MEXT, Japan [18002011]
- JSPS
- Grants-in-Aid for Scientific Research [18002011] Funding Source: KAKEN
Highly enantioselective aerobic oxidative cross-coupling of 2-naphthols with broad substrate scope was achieved using an iron(salan) complex as the catalyst. Enantiomeric excesses of the products ranged from 87 to 95%. The scope of the cross-coupling reaction was found to be different from that of the homocoupling reaction under the same reaction conditions.
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