Direct coupling of nucleophiles with nitroaromatic compounds via fluoride-promoted oxidative nucleophilic aromatic substitution for hydrogen
I Huertas, I Gallardo, J Marquet
Index: Huertas, Inma; Gallardo, Iluminada; Marquet, Jordi Tetrahedron Letters, 2001 , vol. 42, # 20 p. 3439 - 3441
Full Text: HTML
Citation Number: 20
Abstract
Useful yields are achieved in the regioselective direct coupling of amines, amides, and ketones with m-dinitrobenzene, 1-nitronaphthalene, and 1, 3-dinitronaphthalene, through oxidatively activated nucleophilic aromatic substitution for hydrogen promoted by fluoride anions.
Related Articles:
[Chakraborti, Asit K.; Gulhane, Rajesh Tetrahedron Letters, 2003 , vol. 44, # 35 p. 6749 - 6753]
[Sana, Sariah; Rajanna; Ali, Mir Moazzam; Saiprakash Chemistry Letters, 2000 , # 1 p. 48 - 49]
Nucleophilic aromatic substitution for heteroatoms: an oxidative electrochemical approach
[Huertas, Inma; Gallardo, Iluminada; Marquet, Jordi Tetrahedron Letters, 2000 , vol. 41, # 2 p. 279 - 281]
Mild and selective nitration by claycop
[Gigante, Barbara; Prazeres, Angela O.; Marcelo-Curto, Maria J.; Cornelis, Andre; Laszlo, Pierre Journal of Organic Chemistry, 1995 , vol. 60, # 11 p. 3445 - 3447]
[Miyashita, Mitsutomo; Shiina, Isamu; Mukaiyama, Teruaki Bulletin of the Chemical Society of Japan, 1994 , vol. 67, # 1 p. 210 - 215]