Abstract
AbstractHere, a mild and general oxidative radical relay carbocyclization reaction with 2‐arylbenzoimidazoles and cyclic ethers is reported. This method provides an efficient access to a wide range of structurally diverse benzimidazo[2,1‐a]isoquinoline‐6(5H)‐ones under metal‐free conditions. The wide substrate scope, good functional group tolerance, and scale‐up operation of this method are expected to promote its potential applications in biotechnology and pharmacy.magnified image
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