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Please use this identifier to cite or link to this item: http://dspace.bsu.edu.ru/handle/123456789/52115
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dc.contributor.authorPotapov, A. Yu.-
dc.contributor.authorPaponov, B. V.-
dc.contributor.authorPodoplelova, N. A.-
dc.contributor.authorPanteleev, M. A.-
dc.contributor.authorPotapov, M. A.-
dc.date.accessioned2023-03-14T09:07:27Z-
dc.date.available2023-03-14T09:07:27Z-
dc.date.issued2021-
dc.identifier.citationSynthesis of 2H-pyrano[3,2-g]quinolin-2-ones containing a pyrimidinone moiety and characterization of their anticoagulant activity via inhibition of blood coagulation factors Xa and XIa / Potapov A.Yu. [et al.] // Chemistry of Heterocyclic Compounds. - 2021. - Vol.57, №5.-P. 574-580.ru
dc.identifier.urihttp://dspace.bsu.edu.ru/handle/123456789/52115-
dc.description.abstractThe reactions of 7-hydroxy-1,2,2,4-tetramethylhydroquinoline-6-carbaldehydes with methyl 3-oxopentanedioate were used to synthesize 3-oxo-3-(6,8,8,9-tetramethyl-2-oxo-2H-pyrano[3,2-g]quinolin-3-yl)propanoates with various degrees of hydrogenation in the pyridine ring, the condensation of which with carboximidamides provided a series of new 6,8,8,9-tetramethyl-3-(6-oxo-1,6-dihydropyrimidin- 4-yl)-2H-pyrano[3,2-g]quinolin-2-ones. It was found that some compounds of this class exhibited relatively high inhibitory activity against the blood coagulation factors Xа and XIaru
dc.language.isoenru
dc.subjectchemistryru
dc.subjectorganic chemistryru
dc.subjectcarboximidamideru
dc.subjectmethyl 2-oxo-(2H-pyrano[3,2-g]quinolin-3-yl)propanoateru
dc.subjectpyrano[3,2-g]quinolineru
dc.subjectpyrimidineru
dc.subjectfactor Xaru
dc.subjectfactor XIaru
dc.subjectmolecular hybridizationru
dc.titleSynthesis of 2H-pyrano[3,2-g]quinolin-2-ones containing a pyrimidinone moiety and characterization of their anticoagulant activity via inhibition of blood coagulation factors Xa and XIaru
dc.typeArticleru
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