872809-63-7Relevant articles and documents
Metal-free photocatalyzed cross coupling of aryl (heteroaryl) bromides with isonitriles
Li, Xiangguang,Liang, Deqiang,Huang, Wenzhong,Sun, Huanli,Wang, Lvsu,Ren, Mengran,Wang, Baoling,Ma, Yinhai
, p. 7094 - 7099 (2017/11/13)
A visible-light-catalyzed synthesis of 6-aryl substituted phenanthridines from aryl bromides and 2-isocyanobiphenyls at room temperature has been discovered. This metal-free cross-coupling reaction offers rapid and sustainable access to a series of struct
Metal-free radical oxidative decarboxylation/cyclization of acyl peroxides and 2-isocyanobiphenyls
Pan, Changduo,Zhang, Honglin,Han, Jie,Cheng, Yixiang,Zhu, Chengjian
supporting information, p. 3786 - 3788 (2015/03/30)
A metal-free radical oxidative decarboxylation/cyclization of acyl peroxides and 2-isocyanobiphenyls was achieved, leading to 6-aryl phenanthridines as well as 6-alkyl phenanthridines in moderate to good yields. The procedure featured simple conditions and was metal-free and base free. It represents a practical approach to access 6-aryl/alkyl phenanthridines.
Transition-metal-free, visible-light induced cyclization of arylsulfonyl chlorides with 2-isocyanobiphenyls to produce phenanthridines
Gu, Lijun,Jin, Cheng,Liu, Jiyan,Ding, Hongyan,Fan, Baomin
supporting information, p. 4643 - 4645 (2014/05/06)
6-Aryl substituted phenanthridines were synthesized via a visible-light-catalyzed cyclization of 2-isocyanobiphenyls with arylsulfonyl chlorides under oxidant-free and transition-metal-free conditions. This transformation represents an efficient and attractive synthetic utilization of arylsulfonyl chlorides. the Partner Organisations 2014.
