期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 136, 期 4, 页码 1304-1307出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja4117632
关键词
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资金
- NIH/NIGMS [GM-097444]
- NSF
- JSPS
- Grants-in-Aid for Scientific Research [12J10137] Funding Source: KAKEN
A redox-economic method for the direct coupling of olefins that uses an inexpensive iron catalyst and a silane reducing agent is reported. Thus, unactivated olefins can be joined directly to electron-deficient olefins in both intra- and intermolecular settings to generate hindered bicyclic systems, vicinal quaternary centers, and even cyclopropanes in good yield. The reaction is not sensitive to oxygen or moisture and has been performed on gram-scale. Most importantly, it allows access to many compounds that would be difficult or perhaps impossible to access using other methods.
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