134890-53-2Relevant academic research and scientific papers
Regioselective ring opening of 2,2-dicyanooxiranes by 1,3-dinucleophiles in the presence of Lewis acids such as bismuth(III) nitrate pentahydrate [Bi(NO3)3·5H2O] and zirconium(IV) chloride (ZrCl4)
Karbalaei, Mahboobeh,Seifi, Mohammad,Sheibani, Hassan
, p. 4679 - 4686 (2015)
Bismuth(III) nitrate pentahydrate [Bi(NO3)3·5H2O] or zirconium(IV) chloride (ZrCl4) has been shown to catalyze nucleophilic ring opening of 2,2-dicyanooxiranes along with ring closure by 1,3-dinucleophiles such
Regioselective combination of 1,3-dinucleophiles such as 2-mercaptobenzimidazole, 5-mercapto-3-phenyltriazole and potassium thiocyanate with 2,2-dicyanooxiranes
Seifi, Mohammad,Sheibani, Hassan
, p. 191 - 199 (2013/10/21)
A group of heterocyclic compounds of condensed [1,3]thiazole with benzimidazole or triazole derivatives were obtained by the regioselective reactions of the 2,2-dicyanooxiranes with 1H-1,3-benzimidazol-2-thiol or 5-phenyl-4H-1,2,4-triazol-3-thiol respecti
Reaction of cyanoepoxides with 2-mercaptobenzimidazole and 2-aminothiazole and biological assessment of products formed
Jaguelin,Robert,Gayral
, p. 51 - 57 (2007/10/02)
The two carbons of the epoxide ring of the gem-dicyano epoxides and α-cyano α-ester epoxides act as electrophilic centers when these compounds are reacted with 2-mercaptobenzimidazole. The reaction leads to 2,3-dihydrobenzimidazo[2,1-b]-thiazoles. However, such a reactivity of the epoxides is not observed during their reaction with 2-aminothiazoline. Some of the synthetized compounds showed anthelminthic properties.
