57319-72-9Relevant articles and documents
Design and structure-activity relationships anticandidosic of diazaheteroaryl functionalized by Micha?l acceptors
Aboudramane, Kone,Doumade, Zon,Drissa, Sissouma,Jean-Paul, N'Guessan D.,Mahama, Ouattara,Mamidou, Koné Witabouna,Songuigama, Coulibaly
, p. 117 - 133 (2022/02/14)
Benzimidazole and imidazopyridine heterocycles associated with Micha?l acceptors have shown strong anticandidosic potential in our previous work. After a decade of research, we have designed, synthesized and evaluated the anticandidosic activities of seve
Anhydrous zinc chloride catalysis in carbonyl-methylene condensations: Synthesis of arylidene acetonitriles and arylidene heterocycles
Rao, P. Shanthan,Venkataratnam, R. V.
, p. 484 - 486 (2007/10/02)
Anhydrous zinc chloride has been found to be an efficient catalyst in carbonyl-methylene condensation reactions.The synthesis of arylidene acetonitriles (6a-g, 7a-g) and arylidene heterocycles (8a-e, 9a-e) have been accomplished in high yields and good purity.
Reactions of cyanomethylbenzimidazoles. Part II. Reaction of cyanomethylbenzimidazoles with aldehydes methylketones and nitroso compounds.
Sawlewicz,Milczarska,Manowska
, p. 187 - 201 (2007/10/09)
Position of CH2CN group in the benzimidazole system determines the activity of hydrogen atoms of CH2 group in condensation reactions. Some of the obtained compounds show high tuberculostatic activity.