琥珀酰亚胺
化学
废止
苯并咪唑
丁二酰亚胺
铑
催化作用
组合化学
化学选择性
表面改性
功能群
荧光
基质(水族馆)
有机化学
物理化学
地质学
物理
聚合物
海洋学
量子力学
作者
Mohammad Aslam,Sonaimuthu Mohandoss,Yong Rok Lee
出处
期刊:Organic Letters
[American Chemical Society]
日期:2021-08-03
卷期号:23 (16): 6206-6211
被引量:41
标识
DOI:10.1021/acs.orglett.1c01793
摘要
A novel Rh-catalyzed cascade C-H activation/annulation of 2-arylbenzimidazoles with maleimides is reported. Rapid chemoselective access to two structurally distinct succinimide-bearing benzoimidazoisoquinolinones is achieved, depending on the acidic and basic conditions. This atom- and step-economic strategy features a wide substrate scope, excellent functional group tolerance, and site-specific functionalization. Application of the methodology yields a novel benzimidazole-based probe as a fluorescent chemosensor for the nanomolar detection of Hg2+, Cu2+, and Fe3+ ions.
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