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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 |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| WoS 873 .pdf Restricted Access | 179.2 kB | Adobe PDF | View/Open | |
| scopusresults 1340 .pdf Restricted Access | 56.11 kB | Adobe PDF | View/Open |
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