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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/123456789/32643
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dc.contributor.authorDemidov, O. P.-
dc.contributor.authorДемидов, О. П.-
dc.date.accessioned2026-02-20T08:09:16Z-
dc.date.available2026-02-20T08:09:16Z-
dc.date.issued2026-
dc.identifier.citationOsyanin, V. A., Demidov, O. P. Synthesis of 7a,8-Dihydrobenzo[5,6]chromeno[2,3-b]pyrrol-9(11H)-ones // Russian Journal of General Chemistry. - 2026. - 96 (2). - art. no. 6. - DOI: 10.1134/S1070363225606283ru
dc.identifier.urihttps://dspace.ncfu.ru/handle/123456789/32643-
dc.description.abstractA method for the synthesis of 7a,8-dihydrobenzo[5,6]chromeno[2,3-b]pyrrol-9(11H)-ones from β-methoxalyl-substituted 1H-benzo[f]chromenes and primary aliphatic amines in the presence of nitromethane has been developed. A possible reaction route is proposed that includes the Henry reaction, the aza-Michael reaction, intramolecular nucleophilic addition, and the retro-aza-Henry reaction as the main stages.ru
dc.language.isoenru
dc.publisherPleiades Publishingru
dc.relation.ispartofseriesRussian Journal of General Chemistry-
dc.subject7a,8-dihydrobenzo[5,6]chromeno[2,3-b]pyrrol-9(11H)-onesru
dc.subjectCascade reactionsru
dc.subjectPrimary aminesru
dc.subjectβ-methoxalyl-substituted 1H-benzo[f]chromenesru
dc.titleSynthesis of 7a,8-Dihydrobenzo[5,6]chromeno[2,3-b]pyrrol-9(11H)-onesru
dc.typeСтатьяru
vkr.instХимический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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