Synthetic Communications

One-pot reductive mono-N-alkylation of aromatic nitro compounds using nitriles as alkylating reagents

S Neogi, D Naskar

Index: Neogi, Subhasish; Naskar, Dinabandhu Synthetic Communications, 2011 , vol. 41, # 13 p. 1901 - 1915

Full Text: HTML

Citation Number: 2

Abstract

Abstract A one-pot, simple, selective, and efficient protocol for the synthesis of aromatic secondary amines from various nitro arenes and nitriles in the presence of 10% Pd/C catalyst under H2 at atmospheric pressure and ambient temperature in tetrahydrofuran is illustrated. The scope and limitations of this method have been examined.

Related Articles:

1H, 2H, 19F, 14N ENDOR and TRIPLE resonance investigations of substituted flavin radicals in their different protonation states

[Weilbacher, E.; Helle, N.; Elsner, M.; Kurreck, H.; Mueller, F.; Allendoerfer, R. D. Magnetic Resonance in Chemistry, 1988 , vol. 26, p. 64 - 72]

More Articles...