期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 135, 期 44, 页码 16372-16375出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja409661n
关键词
-
资金
- Yamaguchi University [24750043]
- MEXT, Japan
- Grants-in-Aid for Scientific Research [24750043] Funding Source: KAKEN
alpha-Halocarbonyl compounds undergo beta-hydrogen elimination to give conjugated olefins in the presence of a transition-metal catalyst. However, a copper/triamine catalyst system can induce the alkylative Mizoroki-Heck reaction of styrenes with tertiary-alkyl halides possessing a withdrawing group under very mild conditions. This reaction provides an efficient synthetic methodology for tertiary-alkylated styrenes.
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