121513-89-1Relevant articles and documents
Nickel-catalyzed Kumada Cross-coupling Reaction for the Synthesis of 2,4-Diarylquinazolines
Ye, Xinglin,Yuan, Zhihan,Zhou, Yirong,Yang, Qin,Xie, Yepeng,Deng, Zhihong,Peng, Yiyuan
, p. 1956 - 1962 (2016)
A series of 2,4-diarylquinazolines have been successfully synthesized via the Ni-catalyzed cross-coupling reaction of quinazoline-4-tosylates and aryl Grignard reagents, which provided alternative straightforward approaches for the introduction of aryl groups to quinazolines at C-4 position.
Synthesis of 4-arylquinazolines by arylation of quinazolin-4-ones under mild conditions
Qiu, Guanyinsheng,Huang, Ping,Yang, Qin,Lu, Hui,Xu, Jingshi,Deng, Zhihong,Zhang, Ming,Peng, Yiyuan
supporting information, p. 3131 - 3136 (2013/12/04)
An efficient route to 4-arylquinazolines via arylation of quinazolin-4-ones under mild condition is described. The reaction is carried out by the palladium-catalyzed coupling of quinazolin-4-ones with arylboronic acids in the presence of TsCl leading to 4-arylquinazolines in good to excellent yields. Georg Thieme Verlag Stuttgart New York.