Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/14216
Title: Synthesis and biological activity of 8-(dialkylamino)-3-aryl-6-oxo-2,4-dicyanobicyclo[3.2.1]octane-2,4-dicarboxylic acids diethyl esters
Authors: Dotsenko, V. V.
Доценко, В. В.
Keywords: Aza-Piancatelli rearrangement;Bicyclo[3.2.1]octane;Furfural;Nazarov reaction;Stenhouse salts
Issue Date: 2020
Publisher: Pleiades journals
Citation: Ismiyev, 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 1418-1425
Series/Report no.: Russian Journal of General Chemistry
Abstract: Cascade 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 effect
URI: http://hdl.handle.net/20.500.12258/14216
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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