4610-75-7Relevant articles and documents
Pd-catalyzed C-S activation for [3 + 3] annulation of 2-(methylthio) benzofuran-3-carboxylates and 2-hydroxyphenylboronic acids: Synthesis of coumestan derivatives
Liu, Jingxin,Liu, Yingjie,Du, Wenting,Dong, Ying,Liu, Jun,Wang, Mang
, p. 7293 - 7297 (2013)
Pd-catalytic C-S activation was successfully applied to initiate the cross-coupling of (2-methylthio-3-ester)benzofurans with 2-hydroxyphenylboronic acids and sequential intramolecular transesterification process under Liebeskind-Srogl conditions. Thus, a novel [3 + 3] annulation strategy for efficient synthesis of coumestan derivatives has been developed from readily available starting materials.
Design, synthesis and in vitro anti-bacterial activities of benzofuran-isatin hybrids
Wang, Yin-Ling,Zhao, Shi-Jia,Liu, Yi,Xu, Zhi
, p. 687 - 710 (2021/02/06)
A series of novel benzofuran-isatin hybrids 6a-x tethered through propylene, butylene, pentylene and hexylene were designed, synthesized and evaluated for their in vitro antibacterial activities against a panel of clinically important Gram-positive and Gr
Benzofuran-isatin-hydroxylimine/thiosemicarbazide hybrids: Design, synthesis and in vitro anti-mycobacterial activity evaluation
Zhang, Yaohuan,Wang, Ruo,Zhang, Tesen,Yan, Weitao,Chen, Yihong,Zhang, Yanping,Zhou, Muyang
, p. 653 - 655 (2019/01/04)
A series of novel benzofuran-isatin-hydroxylimine/thiosemicarbazide hybrids were designed, synthesized and evaluated for their in vitro anti-TB activities against drug-sensitive MTB H37Rv and MDR-TB isolates as well as cytotoxicity. All benzofu
