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Au(Ⅰ)-Catalyzed 6-endo-dig Cyclizations of Aromatic 1,5-Enynes to 2-(Naphthalen-2-yl)anilines Leading to Divergent Syntheses of Benzo[α]carbazole,Benzo[c,h]cinnoline and Dibenzo[i]phenanthridine Derivatives
作者姓名:Jiayue Fu  Bingbing Li  Xiugui Wang  Qida Liang  Xiaoshi Peng  Lu Yang  Tao Wan  Xinxiu Wang  Bin Lin  Maosheng Cheng  Yongxiang Liu
作者单位:Key Laboratory of Structure-Based Drug Design and Discovery(Shenyang Pharmaceutical University);Wuya College of Innovation;Institute of Drug Research in Medicine Capital of China;Liaoning Kangboshi Pharmaceutical Co.
基金项目:the financial support of the National Natural Science Foundation of China(Grants 21977073);the Liao-ning BaiQianWan Talents Program;Liaoning Revitalization Tale nts Program;the program for the innoyative research team of the Ministry of Education;the program for the Liaoning innovative research team in university.
摘    要:A gold(Ⅰ)-catalyzed 6-endo-dig cyclization of aromatic 1,5-enynes was developed to synthesize 2-(naphthalen-2-yl)anilines.The functional group tolerance of this cyclization was examined systematically and a possible mechanism was proposed.The derivatization of 2-(naphthalen-2-yl)aniline was carried out to facile access to benzoα]carbazole,benzoc,h]cinnoline and dibenzoi]phenanthridine derivatives in a divergent way.

关 键 词:Gold  Homogeneous  catalysis  6-endo-dig  Cyclization  Heterocycles  Divergent  synthesis
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