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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/18254
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dc.contributor.authorDemidov, O. P.-
dc.contributor.authorДемидов, О. П.-
dc.date.accessioned2021-11-11T08:43:32Z-
dc.date.available2021-11-11T08:43:32Z-
dc.date.issued2021-
dc.identifier.citationOsipov, D. V., Rashchepkina, D. А., Аrtemenko, A. А., Demidov, O. P., Osyanin, V. А. Nucleophilic dearomatization of 3-nitrobenzofurans by the action of 2-(1-arylethylidene)malononitriles // Chemistry of Heterocyclic Compounds. - 2021. - Том 57. - Выпуск 10. - Стр.: 996 - 1001. - DOI 10.1007/s10593-021-03013-2ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/18254-
dc.description.abstractWhen 2-(1-arylethylidene)malononitriles act upon 3-nitrobenzofurans in the presence of triethylamine, the furan ring opens and triethylammonium 2-aryl-1,1-dicyano-5-nitropenta-2,4-dien-1-ides are formed. The obtained salts containing the chromophoric 1,1-dicyanopentadienide fragment are of interest as anionic polymethine dyesru
dc.language.isoenru
dc.publisherSpringerru
dc.relation.ispartofseriesChemistry of Heterocyclic Compounds-
dc.subject2-(1-arylethylidene)malononitrilesru
dc.subjectNucleophilic dearomatizationru
dc.subject1,1-dicyanopenta-2,4-dien-1-ide anionru
dc.subject3-nitrobenzofuransru
dc.subjectMichael reactionru
dc.titleNucleophilic dearomatization of 3-nitrobenzofurans by the action of 2-(1-arylethylidene)malononitrilesru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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