19816-42-3Relevant articles and documents
Cytisine-flavonoid conjugates: Synthesis and antitumor structure-activity relationship research
Bao, Xiaoze,Cai, Yue,Li, Xing-Nuo,Liu, Renhao,Sun, Xuanrong,Ye, Xinyi,Zhang, Tianwei
, (2020)
In research of anti-triple negative breast cancer (TNBC) agents, a series of cytisine-flavonoid conjugates (A-1 ~ G-1) were designed and synthesized in high yields with (?)-cytisine and flavonoids via N,N-4-dimethyl-4-aminopyridine (DMAP)-catalyzed synthe
An efficient approach to dihydrofuroflavonoids via palladium-catalyzed annulation of 1,3-dienes by 0-iodoacetoxyflavonoids
Rozhkov, Roman V.,Larock, Richard C.
, p. 1854 - 1858 (2007/10/03)
The palladium-catalyzed annulation of 1,3-dienes by o-iodoacetoxyflavonoids provides an efficient approach to biologically interesting dihydrofuroflavonoids. This reaction is very general, stereo-and regioselective, and a wide variety of terminal, cyclic and internal 1,3-dienes can be utilized.