72934-63-5Relevant academic research and scientific papers
Flavonoid-triazolyl hybrids as potential anti-hepatitis C virus agents: Synthesis and biological evaluation
Zhang, Han,Zheng, Xin,Li, Jichong,Liu, Qingbo,Huang, Xiao-Xiao,Ding, Huaiwei,Suzuki, Ryosuke,Muramatsu, Masamichi,Song, Shao-Jiang
, (2021/04/12)
A series of flavonoid-triazolyl hybrids were synthesized and evaluated as novel inhibitors of hepatitis C virus (HCV). The results of anti-HCV activity assays showed that most of the synthesized derivatives at a concentration of 100 μg/mL inhibited the ge
A short and facile synthetic route to prenylated flavones. Cyclodehydrogenation of prenylated 2'-hydroxychalcones by a hypervalent iodine reagent
Gulacsi, Katalin,Litkei, Gyoergy,Antus, Sandor,Gunda, Tamas E.
, p. 13867 - 13876 (2007/10/03)
The first synthesis of the prenylated flavones kanzonol-D (1), -E (3) and yinyanghuo-C (4) was accomplished by cyclodehydrogenation of the appropriately substituted 2'-hydroxychalcones 16, 14 and 11, respectively, in presence of phenyl-iodine(III) diaceta
