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Electrooxidative Metal‐Free Cyclization of 4‐Arylaminocoumarins with DMF as C1‐Source

Yiyi Weng, Hantao Chen, Nanhui Li, Long Yang, Lutz Ackermann

2021Advanced Synthesis & Catalysis28 citationsDOI

Abstract

Abstract An environmentally‐benign electrochemical approach for the construction of quinoline derivatives employing N , N ‐dimethylformamide (DMF) as the methine source has been devised by cyclization of 4‐(phenylamino)‐ 2H ‐chromen‐2‐ones. In a user‐friendly undivided cell, 6H ‐chromeno[4,3‐ b ]quinolin‐6‐ones were obtained under chemical oxidant‐free and transition‐metal‐free conditions in 43–92% yields with high functional tolerance. magnified image

Topics & Concepts

ChemistryQuinolineDimethylformamideEnvironmentally friendlyTransition metalElectrochemistryMetalCombinatorial chemistryOrganic chemistryCatalysisPhysical chemistryElectrodeBiologySolventEcologyRadical Photochemical ReactionsCatalytic C–H Functionalization MethodsSulfur-Based Synthesis Techniques
Electrooxidative Metal‐Free Cyclization of 4‐Arylaminocoumarins with DMF as C1‐Source | Litcius