Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/13662
Title: Reaction of 3-Amino-4,6-diarylthieno[2,3-b]pyridine-2-carboxamides with Ninhydrin
Authors: Dotsenko, V. V.
Доценко, В. В.
Aksenov, N. A.
Аксенов, Н. А.
Aksenova, I. V.
Аксенова, И. В.
Keywords: 2,4-D herbicide antidotes;Heterocyclization;Ninhydrin;Thieno[2,3-b]pyridines;Thorpe–Ziegler reaction
Issue Date: 2020
Publisher: Pleiades Publishing
Citation: Dotsenko, V.V., Muraviev, V.S., Lukina, D.Y., Strelkov, V.D., Aksenov, N.A., Aksenova, I.V., Krapivin, G.D., Dyadyuchenko, L.V. Reaction of 3-Amino-4,6-diarylthieno[2,3-b]pyridine-2-carboxamides with Ninhydrin // Russian Journal of General Chemistry. - 2020. - Volume 90. - Issue 6. - Pages 948-960
Series/Report no.: Russian Journal of General Chemistry
Abstract: The reaction of N-substituted amides of 3-amino-4,6-diarylthieno[2,3-b]pyridine-2-carboxylic acids with ninhydrin in the presence of catalytic amounts of sulfuric acid gave 1′-spiro[indene-2,2′-pyrido[3′,2′:4,5]thieno[3,2-d]pyrimidine]-1,3,4′(3′H)-triones. Structure of a number of key compounds was studied using 2D NMR spectroscopy; the bioavailability parameters of the obtained compounds in silico were calculated. In a laboratory experiment, a moderate antidote effect was revealed with respect to the 2,4-D herbicide for one compound
URI: http://hdl.handle.net/20.500.12258/13662
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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