Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/8307
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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.accessioned2019-11-13T10:05:28Z-
dc.date.available2019-11-13T10:05:28Z-
dc.date.issued2019-
dc.identifier.citationBuryi, D.S., Dotsenko, V.V., Aksenov, N.A., Aksenova, I.V. Synthesis and Properties of New Fluorine-Containing Thieno[2,3-b]pyridine Derivatives // Russian Journal of General Chemistry. - 2019. - Volume 89. - Issue 9. - Pages 1744-1751ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/8307-
dc.description.abstractCyanothioacetamide reacted with 1,1,5,5-tetrafluoroacetylacetone to give 4,6-bis(difluoromethyl)-2-thioxo-1,2-dihydropyridine-3-carbonitrile, and alkylation of the latter with α-chloroacetamides afforded 3-amino-4,6-bis(difluoromethyl)thieno[2,3-b]pyridine-2-carboxamides. The structure of the key compounds was proved using two-dimensional NMR techniques. In silico analysis of potential biological activity and bioavailability of the synthesized compounds was performedru
dc.language.isoenru
dc.publisherPleiades Publishingru
dc.relation.ispartofseriesRussian Journal of General Chemistry-
dc.subjectCyanothioacetamideru
dc.subjectGuareschi-Thorpe reactionru
dc.subjectIn silico biological activityru
dc.subjectOrganic fluoridesru
dc.subjectThieno[2,3-b]pyridinesru
dc.subjectThorpe-Ziegler cyclizationru
dc.titleSynthesis and properties of new fluorine-containing thieno[2,3-b]pyridine derivativesru
dc.typeСтатьяru
vkr.amountPages 1744-1751ru
vkr.instИнститут математики и естественных наук-
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