期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 134, 期 20, 页码 8380-8383出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja302223p
关键词
-
资金
- University of Iowa
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [0946779] Funding Source: National Science Foundation
The rhodium-catalyzed regio- and enantioselective amination of racemic tertiary allylic trichloroacetimidates with a variety of aniline nucleophiles is a direct and efficient route to chiral alpha,alpha-disubstituted allylic N-arylamines. We describe the first dynamic kinetic asymmetric transformations of racemic tertiary allylic electrophiles with anilines utilizing a chiral diene-ligated rhodium catalyst. The method allows for the formation of alpha,alpha-disubstituted allylic N-arylamines in moderate to good yields with good to excellent levels of regic- and enantioselectivity.
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