摘要
新结构的黄酮衍生物,由于其多样化的生物活性而在药物发展中备受人们的重视.这里,报道了一种以Se粉为原料,使用铜化合物作为催化剂,通过C-H官能化来合成含ArSe取代基的黄酮衍生物,反应具有良好的选择性和较高的收率.
New flavone derivatives are highly valued in drug discovery due to their diversity of important bioactivities.Herein,one simple Cu-catalyzed method of constructing C-Se bonds on flavone structures using convenient Se powder via C-H functionalization is reported,regioselectively affording ArSe-substituted flavone derivatives in good yields.
作者
冯春来
朱杰
唐秋洁
周爱华
Feng Chunlai;Zhu Jie;Tang Qiujie;Zhou Aihua(Pharmacy School,Jiangsu University,Zhenjiang 212013)
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2019年第4期1187-1192,共6页
Chinese Journal of Organic Chemistry
基金
Project supported by Jiangsu University(No.1281290006)~~