Halogenation of Aromatic Compounds by N-chloro-, N-bromo-, and N-iodosuccinimide
K Tanemura, T Suzuki, Y Nishida, K Satsumabayashi…
Index: Tanemura, Kiyoshi; Suzuki, Tsuneo; Nishida, Yoko; Satsumabayashi, Koko; Horaguchi, Takaaki Chemistry Letters, 2003 , vol. 32, # 10 p. 932 - 933
Full Text: HTML
Citation Number: 97
Abstract
Halogenation of aromatic compounds is one of the most im- portant reactions in organic synthesis. The most commonly used reagents for this purpose are bromine and chlorine in the pres- ence of iron halide. In terms of ease of handling in laboratories, N-bromo- (NBS) and N-chlorosuccinimide (NCS) will be supe- rior halogenating reagents if benzylic halogenation is sup- pressed. Schmid reported that benzene and toluene gave nuclear brominated ...
Related Articles:
[Nobuta, Tomoya; Fujiya, Akitoshi; Hirashima, Shin-Ichi; Tada, Norihiro; Miura, Tsuyoshi; Itoh, Akichika Tetrahedron Letters, 2012 , vol. 53, # 39 p. 5306 - 5308]
[Marchal, Joel; Bodiguel, Jacques; Fort, Yves; Caubere, Paul Journal of Organic Chemistry, 1995 , vol. 60, # 26 p. 8336 - 8340]
[Marchal, Joel; Bodiguel, Jacques; Fort, Yves; Caubere, Paul Journal of Organic Chemistry, 1995 , vol. 60, # 26 p. 8336 - 8340]
[Marchal, Joel; Bodiguel, Jacques; Fort, Yves; Caubere, Paul Journal of Organic Chemistry, 1995 , vol. 60, # 26 p. 8336 - 8340]
The carbonylation of phenyl bromide and its derivatives under visible light irradiation
[Zhong, Wen Hui; Cui, Ying Na; Li, Shen Min; Jia, Ying Ping; Yin, Jing Mei Chinese Chemical Letters, 2012 , vol. 23, # 1 p. 29 - 32]