期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 86, 期 22, 页码 16059-16067出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.1c01271
关键词
-
资金
- National Natural Science Foundation of China [21602078]
- Pearl River Talent Program of Guangdong Province (Youth Top-Notch Talent) [2017GC010302]
- Guangdong Basic and Applied Basic Research Foundation [2019A1515011743]
- Jinan University
A practical protocol for synthesizing 3-substituent-2-(azol-1-yl)indole derivatives has been developed through an electrochemical oxidative cross coupling process. This strategy tolerates a variety of functional groups and is suitable for gram scale synthesis, as well as late-stage functionalization of bioactive molecules.
A practical protocol to synthesize 3-substituent-2-(azol-1-yl)indole derivatives has been developed via an electrochemical oxidative cross coupling process under mild conditions. This electro-oxidative C-N bond formation strategy tolerates a range of functional groups and is amenable to gram scale synthesis. Moreover, this method was applied to the late-stage functionalization of bioactive molecules.
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