化学
胺化
咔唑
分子内力
芳基
乌尔曼反应
组合化学
有机化学
基质(水族馆)
还原胺化
乙酰化
铜
催化作用
烷基
地质学
海洋学
基因
生物化学
作者
Jaeyoung Ban,Minkyung Lim,Saira Shabbir,Junghyun Baek,Hakjune Rhee
出处
期刊:Synthesis
[Georg Thieme Verlag KG]
日期:2019-11-26
卷期号:52 (06): 917-927
被引量:7
标识
DOI:10.1055/s-0039-1690759
摘要
We synthesized various carbazoles from anilines through a three-step process with good overall yields (up to 48%). This process comprises N-acetylation, copper(0)-mediated Ullmann homocoupling, and acid-mediated intramolecular amination. It permits various functional groups on the substrate. Scale-up of the developed three-step synthetic route to carbazoles was also demonstrated.
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