N-Arylation of carbazole by microwave-assisted ligand-free catalytic CuI reaction
JK Kwon, JH Cho, YS Ryu, SH Oh, EK Yum
Index: Kwon, Jae Kwan; Cho, Joong Hyun; Ryu, Young-Sil; Oh, Se Hwan; Yum, Eul Kgun Tetrahedron, 2011 , vol. 67, # 26 p. 4820 - 4825
Full Text: HTML
Citation Number: 19
Abstract
Abstract N-Arylation of carbazole has been achieved in high yields within 1 h using a microwave-assisted catalytic CuI reaction with no organic ligand. The N-arylation can be performed by various arylhalides, such as phenyl, pyridine, thiophene, and thiazole moieties. Specifically, N-arylated bromocarbazoles were converted into useful synthetic intermediates for functionalized carbazole materials.
Related Articles:
[Chu, Jean-Ho; Lin, Pi-Shan; Lee, Ya-Ming; Shen, Wei-Ting; Wu, Ming-Jung Chemistry - A European Journal, 2011 , vol. 17, # 48 p. 13613 - 13620]
[Chu, Jean-Ho; Lin, Pi-Shan; Lee, Ya-Ming; Shen, Wei-Ting; Wu, Ming-Jung Chemistry - A European Journal, 2011 , vol. 17, # 48 p. 13613 - 13620]
[Chu, Jean-Ho; Lin, Pi-Shan; Lee, Ya-Ming; Shen, Wei-Ting; Wu, Ming-Jung Chemistry - A European Journal, 2011 , vol. 17, # 48 p. 13613 - 13620]
[Chu, Jean-Ho; Lin, Pi-Shan; Lee, Ya-Ming; Shen, Wei-Ting; Wu, Ming-Jung Chemistry - A European Journal, 2011 , vol. 17, # 48 p. 13613 - 13620]
[Chu, Jean-Ho; Lin, Pi-Shan; Lee, Ya-Ming; Shen, Wei-Ting; Wu, Ming-Jung Chemistry - A European Journal, 2011 , vol. 17, # 48 p. 13613 - 13620]