NaClO-Mediated Cross Installation of Indoles and Azoles Benefits Anticancer Hit Discovery.
Changjun YuRuiyao EXiao-Wei ZhangWen-Qian HuGuangjun BaoYiping LiYuyang LiuZeyuan HeJingyue LiWen MaLing-Yun MouRui WangWangsheng SunPublished in: ChemMedChem (2022)
Innovations in synthetic chemistry have a profound impact on the drug discovery process, and will always be a necessary driver of drug development. As a result, it is of significance to develop novel simple and effective synthetic installation of medicinal modules to promote drug discovery. Herein, we have developed a NaClO-mediated cross installation of indoles and azoles, both of which are frequently encountered in drugs and natural products. This effective toolbox provides a convenient synthetic route to access a library of N-linked 2-(azol-1-yl) indole derivatives, and can be used for late-stage modification of drugs, natural products and peptides. Moreover, biological screening of the library has revealed that several adducts showed promising anticancer activities against A549 and NCI-H1975 cells, which give us a hit for anticancer drug discovery.