Multicomponent Reaction of 2-aminobenzimidazole, Arylglyoxals, and 1,3-cyclohexanedione View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2015-04

AUTHORS

Olesya N. Petrova, Lali L. Zamigajlo, Konstantin S. Ostras, Svetlana V. Shishkina, Oleg V. Shishkin, Alexander V. Borisov, Vladimir I. Musatov, Maria G. Shirobokova, Victoria V. Lipson

ABSTRACT

Three-component reactions of 2-aminobenzimidazole with arylglyoxals and 1,3-cyclohexanedione have been studied under conventional heating and microwave irradiation. Different product types including the Michael adduct and fused heterocyclic systems were obtained. Conditions for the selective formation of 12-aroylbenzimidazo[2,1-b]quinazolin-1(2H)-ones and 3-oxo-2-(2-aryl-1H-imidazo[1,2-a]-benzimidazol-9-ium-3-yl)cyclohex-1-enolates have been determined. The structures of all compound types were established by an X-ray diffraction study. More... »

PAGES

310-319

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-015-1700-y

DOI

http://dx.doi.org/10.1007/s10593-015-1700-y

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1027468377


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