1265071-80-4Relevant academic research and scientific papers
Thermally induced formal [3+2] cyclization of ortho-aminoaryl-tethered alkylidenecyclopropanes: Facile synthesis of furoquinoline and thienoquinoline derivatives
Yu, Liu-Zhu,Hu, Xu-Bo,Xu, Qin,Shi, Min
supporting information, p. 2701 - 2704 (2016/02/18)
We have developed a facile synthetic method to access furoquinoline and thienoquinoline derivatives via a thermally induced ring-opening and cyclization reaction from ortho-aminoaryl-tethered alkylidenecyclopropanes with the in situ generation of isocyana
Structure-activity relationships study of 6-chloro-4-(2-chlorophenyl)-3-(2- hydroxyethyl) quinolin-2(1H)-one derivatives as novel non-nucleoside anti-hepatitis B virus agents
Guo, Rui-Hua,Zhang, Quan,Ma, Yun-Bao,Luo, Jie,Geng, Chang-An,Wang, Li-Jun,Zhang, Xue-Mei,Zhou, Jun,Jiang, Zhi-Yong,Chen, Ji-Jun
experimental part, p. 307 - 319 (2011/02/27)
A series of novel 6-chloro-4-(2-chlorophenyl)-3-(2-hydroxyethyl) quinolin-2(1H)-one derivatives were synthesized and evaluated for anti-hepatitis B virus (anti-HBV) activities in vitro to explore their structure-activity relationships (SARs). Most of the
