期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 16, 期 33, 页码 5969-5972出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ob00941d
关键词
-
资金
- Japan Society for the Promotion of Science (JSPS)
- Ministry of Education, Culture, Sports, Science and Technology (MEXT)
- Japan Science and Technology Agency (JST)
- MERIT program
- University of Tokyo
- JSPS Research Fellowships for Young Scientists
Catalytic alkylation reactions of weakly acidic carbonyl and related pronucleophiles such as amides, esters, and sulfonamides with substituted alkenes have been reported. In the presence of a strong Bronsted base catalyst system, potassium hexamethyldisilazide and 18-crown-6 ether, the desired reactions proceeded in high yields at ambient temperature with a wide substrate scope. These are atomeconomical catalytic alkylation reactions of carbonyl and related compounds.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据