Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/22947
Title: Synthesis and Structure of 4-Aryl-3,6-dioxo-2,3,4,5,6,7-hexahydroisothiazolo[5,4-b]pyridine-5-carbonitriles
Authors: Dotsenko, V. V.
Доценко, В. В.
Aksenov, N. A.
Аксенов, Н. А.
Aksenova, I. V.
Аксенова, И. В.
Keywords: Active methylene thioamides;Monothiomalondiamide;Oxidation;DMSO;Isothiazolo[5,4-b]pyridines;Calculated biological activity
Issue Date: 2022
Citation: Dotsenko, V.V., Jassim, N.T., Temerdashev, A.Z., Aksenov, N.A., Aksenova, I.V. Synthesis and Structure of 4-Aryl-3,6-dioxo-2,3,4,5,6,7-hexahydroisothiazolo[5,4-b]pyridine-5-carbonitriles // Russian Journal of General Chemistry. - 2022. - 92(12), pp. 2861 - 2869. - DOI: 10.1134/S1070363222120386
Series/Report no.: Russian Journal of General Chemistry
Abstract: Oxidation of triethylammonium 6-amino-4-aryl-3-carbamoyl-5-cyano-1,4-dihydropyridine-2-thiolates with DMSO–HCl system leads to the formation of novel 4-aryl-3,6-dioxo-2,3,4,5,6,7-hexahydroisothiazolo[5,4-b]-pyridine-5-carbonitiriles. Structure of the obtained compounds was studied using two-dimensional NMR spectros-copy and HRMS methods. An in silico predictive analysis was carried out to identify bioavailability parameters and possible protein targets for the obtained compounds.
URI: http://hdl.handle.net/20.500.12258/22947
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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