66373-83-9Relevant academic research and scientific papers
Palladium-catalyzed C-2 selective arylation of quinolines
Ren, Xiaoyu,Wen, Ping,Shi, Xiaokang,Wang, Yuling,Li, Jian,Yang, Sizhuo,Yan, Hao,Huang, Guosheng
, p. 5194 - 5197 (2013)
An efficient method for the Pd-catalyzed regioselective C-2 arylation of quinolines is presented. Reactions of various substituted quinolines and unactivated arenes have been conducted under mild conditions. The result shows good product yields of 2-arylq
One-pot synthesis and fluorescence properties of 2-arylquinolines
Sueki, Shunsuke,Okamoto, Chiharu,Shimizu, Isao,Seto, Keisuke,Furukawa, Yukio
supporting information; experimental part, p. 385 - 390 (2010/07/09)
The one-pot synthesis of 2-arylquinoline with arylamines, arylaldehyde, and 1,1-diethoxyethane were studied using a catalytic amount ytterbium triflate. Various 2-arylquinolines showed fluorescence properties and the fluorescence was quenched by introduci
The Role of Exciplexes in the Photoreduction of Quinolinemethanols
Epling, Gary A.,Lin, Kuei-Ying,Kumar, Anil
, p. 425 - 429 (2007/10/02)
The photoreduction of a family of quinolinemethanols has been examined both in the presence and absence of exciplex-forming additives.Photoreduction of the alcohol group and cleavage of the side chain occurs on direct photolysis.However, irradiation with triethylamine led to predominant cleavage of the side chain while irradiation with 1,3-dicyanobenzene predominantly led to photoreduction of the alcohol functionality.A variety of other experiments supported the involvement of exciplexes in these transformations.
