Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/22946
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dc.contributor.authorDotsenko, V. V.-
dc.contributor.authorДоценко, В. В.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenova, I. V.-
dc.contributor.authorАксенова, И. В.-
dc.date.accessioned2023-03-03T12:19:09Z-
dc.date.available2023-03-03T12:19:09Z-
dc.date.issued2022-
dc.identifier.citationDotsenko, V.V., Khalatyan, K.V., Russkikh, A. A., Varzieva, E.A., Kramareva, D. A., Vasilin, V.K., Aksenov, N. A., Aksenova I.V. Synthesis and Some Properties of 2-Amino-4-aryl-6-hexyl-7-hydroxy-4H-chromene-3-carbonitriles // Russian Journal of General Chemistry. - 2022. - 92(12), pp. 2850-2860. - DOI: 10.1134/S1070363222120374ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/22946-
dc.description.abstractThree-component condensation of aromatic aldehydes with malononitrile and 4-hexylresorcinol in toluene in the presence of a base leads to the formation of 2-amino-4-aryl-6-hexyl-7-hydroxy-4H-chromene- 3-carbonitriles in good yields (79–90%). Structure of the compounds was studied using two-dimensional NMR spectroscopy methods. Bioavailability parameters were predicted in silico, and possible protein targets were predicted by protein-ligand docking.ru
dc.language.isoruru
dc.relation.ispartofseriesRussian Journal of General Chemistry-
dc.subject4-hexylresorcinolru
dc.subjectMalononitrileru
dc.subject2-amino-4H-chromene-3-carbonitrilesru
dc.subject2-amino-4H-pyransru
dc.subjectCalculated biological activityru
dc.titleSynthesis and Some Properties of 2-Amino-4-aryl-6-hexyl-7-hydroxy-4H-chromene-3-carbonitrilesru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
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