1239778-99-4Relevant academic research and scientific papers
Rh(III)-Catalyzed C-H Amidation of 2-Arylindoles with Dioxazolones: A Route to Indolo[1,2-c]quinazolines
Wang, Xiaogang,Zhang, Jin,Chen, Di,Wang, Bo,Yang, Xiufang,Ma, Yangmin,Szostak, Michal
supporting information, p. 7038 - 7043 (2019/09/30)
Rhodium(III)-catalyzed C-H amidation of 2-arylindoles with dioxazolones for the synthesis of indolo[1,2-c]quinazolines is reported. The reaction is compatible with a wide range of electronically diverse 2-arylindoles and dioxazolones, providing indolo[1,2
Selective C?H or N?H Imidoylative Annulation of 2-(2-Isocyanophenyl)-1H-indoles Leading to Diverse Indole-fused Scaffolds
Teng, Fan,Hu, Weiming,Hu, Huaanzi,Luo, Shuang,Zhu, Qiang
, (2019/02/07)
2-(2-Isocyanophenyl)-1H-indoles, a class of functionalized isocyanides containing both aromatic C?H and indolo N?H functionalities, are first applied in selective imidoylative annulation reactions. Scaffolds of 6-aryl 11H-indolo[3,2-c]quinoline and 6-aryl
Selective CH or NH Imidoylative Annulation of 2-(2-Isocyanophenyl)-1H-indoles Leading to Diverse Indole-fused Scaffolds
Teng, Fan,Hu, Weiming,Hu, Huaanzi,Luo, Shuang,Zhu, Qiang
, p. 1414 - 1418 (2019/10/28)
2-(2-Isocyanophenyl)-1H-indoles, a class of functionalized isocyanides containing both aromatic CH and indolo NH functionalities, are first applied in selective imidoylative annulation reactions. Scaffolds of 6-aryl 11H-indolo[3,2-c]quinoline and 6-aryl i
Solvent-dependent copper-catalyzed indolyl C3-oxygenation and N1-cyclization reactions: Selective synthesis of 3 H-indol-3-ones and indolo[1,2- c] quinazolines
Guo, Shenghai,Wang, Fang,Tao, Li,Zhang, Xinying,Fan, Xuesen
, p. 3889 - 3896 (2018/04/14)
A simple and practical procedure for the selective preparation of 3H-indol-3-one and indolo[1,2-c]quinazoline derivatives through copper-catalyzed aerobic oxygenation and intramolecular cyclization reactions of 2-(2-amidoaryl)-1H-indoles in the presence o
Method for synthesizing indole[1,2-c]quinazoline compounds
-
Paragraph 0014; 0015; 0016, (2018/09/08)
The invention discloses a method for synthesizing indole[1,2-c]quinazoline compounds, and belongs to the technical field of organic synthesis. The technical scheme of the invention is that the methodfor synthesizing the indole[1,2-c]quinazoline compounds
Copper-catalyzed sequential Ullmann N-arylation and aerobic oxidative C-H amination: A convenient route to indolo[1,2-c]quinazoline derivatives
Sang, Peng,Xie, Yongju,Zou, Jianwei,Zhang, Yuhong
experimental part, p. 3894 - 3897 (2012/09/21)
An efficient synthesis of indolo[1,2-c]quinazoline derivatives has been developed by copper-catalyzed sequential Ullmann N-arylation and aerobic oxidative C-H amination. The protocol uses readily available 2-(2-halophenyl)-1H-indoles and (aryl)methanamines as the starting materials to afford indolo[1,2-c]quinazolines, which are the core units of hinckdentine A.
Copper-catalyzed cascade synthesis of 1H-indolo[1,2-c]quinazoline derivatives
Zhang, Hao,Jin, Yibao,Liu, Hongxia,Jiang, Yuyang,Fu, Hua
, p. 6798 - 6803 (2013/01/15)
A simple, efficient and practical approach to 1H-indolo[1,2-c]quinazoline derivatives has been developed that uses inexpensive and readily-available catalyst and substrates. The method should provide a new strategy for N-fused heterocycles and will show wide application in organic chemistry and medicinal chemistry. A simple, efficient and practical approach to 1H-indolo[1,2-c] quinazoline derivatives has been developed that uses inexpensive and readily-available catalyst and substrates. The method should provide a new strategy for N-fused heterocycles and will show wide application in organic chemistry and medicinal chemistry. Copyright
