Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/22278
Title: N,N′-Diphenyldithiomalonamide as Methylene Active Thioamide: A First Synthesis of Stable Michael Adducts
Authors: Dotsenko, V. V.
Доценко, В. В.
Aksenov, N. A.
Аксенов, Н. А.
Aksenova, I. V.
Аксенова, И. В.
Keywords: Active methylene thioamides;Stable Michael adducts;Dithiomalondianilide;Meldrum’s acid
Issue Date: 2022
Citation: Dotsenko, V.V., Sinotsko, A.E., Varzieva, E.A., Chigorina, E.A., Aksenov, N.A., Aksenova, I.V. N,N′-Diphenyldithiomalonamide as Methylene Active Thioamide: A First Synthesis of Stable Michael Adducts // Russian Journal of General Chemistry. - 2022. - 92 (11), pp. 2530-2535. - DOI: 10.1134/S107036322211041X
Series/Report no.: Russian Journal of General Chemistry
Abstract: N,N′-Diphenyldithiomalonamide reacts with the 4-nitrobenzylidene derivative of Meldrum’s acid (or with Meldrum’s acid and 4-nitrobenzaldehyde) in the presence of a base to form crystalline Michael adducts. Structure of triethylammonium 2,2-dimethyl-5-(1-(4-nitrophenyl)-3-(phenylamino)-2-(phenylcarbamothioyl)-3- thioxopropyl)-4-oxo-4H-1,3-dioxin-6-olate was studied by single crystal X-ray diffraction analysis.
URI: http://hdl.handle.net/20.500.12258/22278
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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