Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/14216
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dc.contributor.authorDotsenko, V. V.-
dc.contributor.authorДоценко, В. В.-
dc.date.accessioned2020-09-29T10:07:48Z-
dc.date.available2020-09-29T10:07:48Z-
dc.date.issued2020-
dc.identifier.citationIsmiyev, A.I., Shoaib, M., Dotsenko, V.V., Ganbarov, K.G., Israilova, A.A., Magerramov, A.M. Synthesis and biological activity of 8-(dialkylamino)-3-aryl-6-oxo-2,4-dicyanobicyclo[3.2.1]octane-2,4-dicarboxylic acids diethyl esters // Russian Journal of General Chemistry. - 2020. - Volume 90. - Issue 8. - Pages 1418-1425ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/14216-
dc.description.abstractCascade reaction of 2 equiv. of furfural (or equimolar amounts of furfural and aromatic aldehyde) with secondary amines and ethyl cyanoacetate afforded diethyl esters of 8-(dialkylamino)-3-aryl-6-oxo-2,4-dicyanobicyclo[3.2.1]octane-2,4-dicarboxylic acids with yields of 37–54%. Antimicrobial activity of a number of obtained compounds in vitro was studied, and biological activity in silico was analyzed. The obtained bicyclo[3.2.1]octanes are inactive or exhibit weak fungicidal activity, but exhibit moderate bactericidal effectru
dc.language.isoenru
dc.publisherPleiades journalsru
dc.relation.ispartofseriesRussian Journal of General Chemistry-
dc.subjectAza-Piancatelli rearrangementru
dc.subjectBicyclo[3.2.1]octaneru
dc.subjectFurfuralru
dc.subjectNazarov reactionru
dc.subjectStenhouse saltsru
dc.titleSynthesis and biological activity of 8-(dialkylamino)-3-aryl-6-oxo-2,4-dicyanobicyclo[3.2.1]octane-2,4-dicarboxylic acids diethyl estersru
dc.typeСтатьяru
vkr.instИнститут математики и естественных наукru
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