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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/18060
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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.contributor.authorShcherbakov, S. V.-
dc.contributor.authorЩербаков, С. В.-
dc.contributor.authorOvcharov, S. N.-
dc.contributor.authorОвчаров, С. Н.-
dc.date.accessioned2021-09-01T13:04:47Z-
dc.date.available2021-09-01T13:04:47Z-
dc.date.issued2021-
dc.identifier.citationDotsenko V. V.; Bespalov A. V.; Russkikh A. A.; Kindop V. K.; Akseno, N. A.; Aksenov, I. V.; Shcherbako, S. V.; Ovcharo, S. N. Reactions of malononitrile dimer with isothiocyanates // Russian Journal of General Chemistry. - 2021. - Том 91. - Выпуск 6. - Стр.: 951 - 965ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/18060-
dc.description.abstractThe reaction of 2-amino-1,1,3-tricyanopropene (malononitrile dimer) withisothiocyanates leads to 1-substituted4,6-diamino-2-thioxo-1,2-dihydropyridine-3,5-dicarbonitriles or4,6-diamino-2-(phenylimino)-2H-thiopyran-3,5-dicarbonitrile, depending on the conditions.Quantum-chemical modeling of the IR spectra and reaction routes for thesynthesized compounds was carried out. Insilico predictive analysis of potential protein targets,compliance with bioavailability criteria, and ADMET parameters wasperformedru
dc.language.isoenru
dc.publisherPleiades journalsru
dc.relation.ispartofseriesRussian Journal of General Chemistry-
dc.subjectIsothiocyanatesru
dc.subjectQuantum chemical calculationsru
dc.subject2-amino-1,1,3-tricyanopropeneru
dc.subject2-thioxopyridinesru
dc.subject2H-thiopyransru
dc.subjectHeterocyclizationru
dc.titleReactions of malononitrile dimer with isothiocyanatesru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
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