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https://dspace.ncfu.ru/handle/20.500.12258/5974| Title: | Synthesis of 4,6-disubstituted 2-thioxo-1,2-dihydropyridine-3-carbonitriles by the reaction of acetylenic ketones with cyanothioacetamide |
| Authors: | Dotsenko, V. V. Доценко, В. В. Aksenova, I. V. Аксенова, И. В. |
| Keywords: | Acetylenic ketones;Bohlmann-Rahtz reaction;Cyanothioacetamide;Thieno-[2,3-b]pyridines;Thorpe-Ziegler reaction |
| Issue Date: | 2019 |
| Publisher: | Pleiades Publishing |
| Citation: | Buryi, D.S., Dotsenko, V.V., Levashov, A.S., Lukina, D.Y., Strelkov, V.D., Aksenov, N.A., Aksenova, I.V., Netreba, E.E. Synthesis of 4,6-Disubstituted 2-Thioxo-1,2-dihydropyridine-3-carbonitriles by the Reaction of Acetylenic Ketones with Cyanothioacetamide // Russian Journal of General Chemistry. - 2019. - Volume 89. -Issue 5. - Pages 886-895 |
| Series/Report no.: | Russian Journal of General Chemistry |
| Abstract: | The reaction of acetylenic ketones with cyanothioacetamide in the presence of morpholine yields 4,6-disubstituted 2-thioxo-1,2-dihydropyridine-3-carbonitriles. Structure of the obtained compounds was proved using 2D NMR spectroscopy, as well as transformations into 3-aminothieno[2,3-b]pyridine-2-carboxamide derivatives |
| URI: | https://www.scopus.com/record/display.uri?eid=2-s2.0-85068040119&origin=resultslist&sort=plf-f&src=s&st1=Synthesis+of+4%2c6-Disubstituted+2-Thioxo-1%2c2-dihydropyridine-3-carbonitriles+by+the+Reaction+of+Acetylenic+Ketones+with+Cyanothioacetamide&st2=&sid=6e4a3f0a57961460ec602538180ac367&sot=b&sdt=b&sl=152&s=TITLE-ABS-KEY%28Synthesis+of+4%2c6-Disubstituted+2-Thioxo-1%2c2-dihydropyridine-3-carbonitriles+by+the+Reaction+of+Acetylenic+Ketones+with+Cyanothioacetamide%29&relpos=0&citeCnt=0&searchTerm= http://hdl.handle.net/20.500.12258/5974 |
| Appears in Collections: | Статьи, проиндексированные в SCOPUS, WOS |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| scopusresults 957 .pdf Restricted Access | 265.31 kB | Adobe PDF | View/Open | |
| WoS 645 .pdf Restricted Access | 103.13 kB | Adobe PDF | View/Open |
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