Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/18254
Title: Nucleophilic dearomatization of 3-nitrobenzofurans by the action of 2-(1-arylethylidene)malononitriles
Authors: Demidov, O. P.
Демидов, О. П.
Keywords: 2-(1-arylethylidene)malononitriles;Nucleophilic dearomatization;1,1-dicyanopenta-2,4-dien-1-ide anion;3-nitrobenzofurans;Michael reaction
Issue Date: 2021
Publisher: Springer
Citation: Osipov, 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/s10593-021-03013-2
Series/Report no.: Chemistry of Heterocyclic Compounds
Abstract: When 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 dyes
URI: http://hdl.handle.net/20.500.12258/18254
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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