1185863-98-2Relevant academic research and scientific papers
Aldehyde as a Traceless Directing Group for Rh(III)-Catalyzed C-H Activation: A Facile Access to Diverse Indolo[1,2- a ]quinolines
Liu, Xingyan,Li, Xiaoyu,Liu, Hu,Guo, Qiang,Lan, Jingbo,Wang, Ruilin,You, Jingsong
, p. 2936 - 2939 (2015)
The aldehyde group has been developed for the first time as a traceless directing group to promote regioselective Rh(III)-catalyzed C-H activation/cyclization of indolyl aldehydes with alkynes. This protocol streamlines access to a variety of appealing indolo[1,2-a]quinoline structures. As illustrative examples, a concise three-step synthesis of indolo[1,2-a]quinoline-based sensitizers is accomplished that exhibits the potential of C-H activation in the construction of organic optoelectronic materials.
Fused ring construction around pyrrole, indole, and related compounds via palladium-catalyzed oxidative coupling with alkynes
Yamashita, Mana,Horiguchi, Hakaru,Hirano, Koji,Satoh, Tetsuya,Miura, Masahiro
scheme or table, p. 7481 - 7488 (2010/01/06)
(Chemical Equation Presented) The selective synthesis of 1,2,3,4-tetrasubstituted carbazoles can be performed effectively through the palladium-catalyzed oxidative coupling reactions of N-substituted indoles or their carboxylic acid derivatives with alkyn
