Please use this identifier to cite or link to this item: https://elib.belstu.by/handle/123456789/48623
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dc.contributor.authorArol, A. S.-
dc.contributor.authorMikhalyonok, S. G.-
dc.contributor.authorBezborodov, V. S.-
dc.contributor.authorKuz’menok, N. M.-
dc.contributor.authorSavelyeu, A.I.-
dc.date.accessioned2022-06-06T08:34:52Z-
dc.date.available2022-06-06T08:34:52Z-
dc.date.issued2021-
dc.identifier.citationSynthesis of Novel 1,2,6-Trisubstituted Indoles Based on Cyclohexenone Scaffold / A. S. Arol [et. al.] // Современные проблемы органической химии : тезисы докладов Всероссийской научной конференции с международным участием, посвященная 90-летию со дня рождения академика В. Н. Коптюга, 9-11 июня 2021 г., Новосибирск. - Новосибирск, 2021. - С. 101.ru
dc.identifier.urihttps://elib.belstu.by/handle/123456789/48623-
dc.description.abstractNew methods of construction of heterocyclic systems are always attracting the interest from organic and medicinal chemists because such substances have significant potential in drug discovery. In this field indoles synthesis occupies a prominent place because of the high biological activity of indoles derivatives. The transformation of γ,δ-unsaturated ketones represents a good method for making pyrrole and indole core. In our work we focused on creating of indole core based on cyclohex-2-enone scaffold.ru
dc.format.mimetypeapplication/pdfru
dc.language.isoenru
dc.subjectheterocyclic systemsru
dc.subjectгетероциклические системыru
dc.subjectindolesru
dc.subjectиндолыru
dc.subjectketonesru
dc.subjectкетоныru
dc.subjectaminesru
dc.subjectаминыru
dc.titleSynthesis of Novel 1,2,6-Trisubstituted Indoles Based on Cyclohexenone Scaffoldru
dc.typeArticleru
dc.identifier.udc547.752-
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