24192-86-7Relevant articles and documents
Heterocyclizations towards 2-arylbenzimidazoles via intermolecular coupling of 2-nitroanilines and aryl aldehydes
Kim, Byeong Hyo,Han, Rongbi,Han, Tae Hee,Jun, Young Moo,Baik, Woonphil,Lee, Byung Min
, p. 5 - 10 (2002)
The reductive intermolecular coupling/heterocyclization reaction between 2-nitroaniline and aromatic aldehydes towards 2-substituted and 1,2-disubstituted benzimidazoles was accomplished in the presence of 2-bromo-2-nitropropane/Zn in a MeOH/CH2/sub
Microwave-assisted one-pot synthesis of 2-(substituted phenyl)-1H- benzimidazole derivatives
Navarrete-Vazquez, Gabriel,Moreno-Diaz, Hermenegilda,Estrada-Soto, Samuel,Torres-Piedra, Mariana,Leon-Rivera, Ismael,Tlahuext, Hugo,Munoz-Muniz, Omar,Torres-Gomez, Hector
, p. 2815 - 2825 (2008/02/11)
A series of 2-(substituted phenyl)-1H-benzimidazole derivatives with various 5-and 6-position substituents (-H, -CH3, -CF3) were synthesized via microwave irradiation using a short synthetic route and Na2S2O5 as oxidant. This simple, fast, and efficient p
Indium-mediated reductive intermolecular coupling reaction of 2-nitroaniline with aromatic aldehydes to benzimidazoles
Kim, Byeong Hyo,Han, Rongbi,Kim, Ji Sook,Jun, Young Moo,Baik, Woonphil,Lee, Byung Min
, p. 41 - 54 (2007/10/03)
2-Nitroaniline and aromatic aldehydes were coupled to give benzimidazoles in high yields in the presence of 2-bromo-2-nitropropane and indium at room temperature.