4.8 Article

Deaminative (Carbonylative) Alkyl-Heck-type Reactions Enabled by Photocatalytic C-N Bond Activation

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 58, 期 8, 页码 2402-2406

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201813689

关键词

amines; carbonylative reactions; deaminative transformations; Heck reaction; photocatalysis

资金

  1. National Science Foundation of China [21822103, 21820102003, 21772052, 21772053, 21572074, 21472057]
  2. Program of Introducing Talents of Discipline to Universities of China (111 Program) [B17019]
  3. International Joint Research Center for Intelligent Biosensing Technology and Health
  4. Natural Science Foundation of Hubei Province [2017AHB047]

向作者/读者索取更多资源

The palladium-catalyzed Heck reaction is a well-known, Nobel Prize winning transformation for producing alkenes. Unlike the alkenyl and aryl variants of the Heck reaction, the alkyl-Heck reaction is still underdeveloped owing to the competitive side reactions of alkyl-palladium species. Herein, we describe the development of a deaminative alkyl-Heck-type reaction that proceeds through C-N bond activation by visible-light photoredox catalysis. A variety of aliphatic primary amines were found to be efficient starting materials for this new process, affording the corresponding alkene products in good yields under mild reaction conditions. Moreover, this strategy was successfully applied to deaminative carbonylative alkyl-Heck-type reactions.

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。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据