化学
异喹啉
吲哚试验
咪唑吡啶
激进的
组合化学
基质(水族馆)
自由基环化
药物化学
立体化学
有机化学
海洋学
地质学
作者
Yun‐Hui Zhao,Yajun Yu,Dandan Hu,Lang Zhao,Wenlin Xie,Zhihua Zhou
标识
DOI:10.1002/ajoc.202000202
摘要
Abstract A peroxide‐mediated oxidation/radical addition/cyclization cascade reaction for the construction of isoquinoline skeleton is reported. The mild metal‐free promoted conditions of this reaction allowed us to synthesize a library of aromatic heterocycle‐substituted isoquinolines with a broad substrate scope, good functional group tolerance, and high atom economy in moderate to good yields. The radical intermediate in this reaction system was captured by TEMPO and confirmed by mass spectrometry (TOF‐MS). Further In vitro antiproliferative activities exhibited significant inhibition of the growth of HepG2, MCF‐7, MGC803 and EC‐9706 human cancer cell lines.
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