56337-98-5Relevant articles and documents
Efficient synthesis of 2,4,5-triaryl-1H-imidazoles from aromatic aldehydes with HMDS catalyzed by N-bromosaccharin (NBSa)
Sedrpoushan, Alireza,Joshani, Zinab,Fatollahi, Leila
, p. 287 - 292 (2014/05/20)
A one-pot efficient procedure for the synthesis of 2, 4, 5-triaryl-1H-imidazole derivatives by the reactions of hexamethyldisilazane and arylaldehydes in the presence of N-bromosaccharin (NBSa) is studied. This new method offers several advantages, such as excellent yields, easy workup, short reaction times, and simple procedure.
Convenient one-pot synthesis of 2,4,5-triaryl-1H-imidazoles from arylaldehydes, benzyl alcohols, or benzyl halides with HMDS in the presence of molecular iodine
Veisi, Hojat,Khazaei, Ardashir,Heshmati, Leila,Hemmati, Saba
experimental part, p. 1231 - 1234 (2012/07/14)
A one-pot efficient procedure for the synthesis of 2,4,5-triaryl-1 H-imidazole derivatives in good to excellent yields by reaction between hexamethyldisilazane and arylaldehydes, benzyl alcohols, benzyl halides in the presence of molecular iodine has been developed. The remarkable advantages of this method are the simple workup procedure, high yields of products, and the availability of reagents.
One-pot synthesis of 2,4,5-triaryl-1 H -imidazoles from arylaldehydes, benzyl alcohols, or benzyl halides with hexamethyldisilazane in molten tetrabutylammonium bromide
Salehi, Javad,Khodaei, Mohammad M.,Khosropour, Ahmad R.
experimental part, p. 459 - 462 (2011/04/16)
A simple and efficient method for the synthesis of 2,4,5-triaryl-1H- imidazole derivatives in good to excellent yields by reaction between hexamethyldisilazane and arylaldehydes, benzyl alcohols, benzyl halides in molten tetrabutylammonium bromide as an inexpensive and non toxic solvent has been developed. The remarkable advantages of this method are the simple workup procedure, high yields of products, the use of an ionic liquid as a green solvent, and the availability of reagents. Georg Thieme Verlag Stuttgart - New York.