Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/8428
Title: Substituted N-(thieno[2,3-b]pyridine-3-yl)acetamides: synthesis, reactions, and biological activity
Authors: Dotsenko, V. V.
Доценко, В. В.
Aksenov, N. A.
Аксенов, Н. А.
Aksenova, I. V.
Аксенова, И. В.
Keywords: Monothiooxamides;Heterocycles;Acylation;Azidoacetamides;Biological activity;Combinatorial chemistry
Issue Date: 2019
Publisher: Springer-Verlag Wien
Citation: Dotsenko, V.V., Buryi, D.S., Lukina, D.Y., Stolyarova, A.N., Aksenov, N.A., Aksenova, I.V., Strelkov, V.D., Dyadyuchenko, L.V. Substituted N-(thieno[2,3-b]pyridine-3-yl)acetamides: synthesis, reactions, and biological activity // Monatshefte fur Chemie. - 2019. - Volume 150. - Issue 11. - Pages 1973-1985
Series/Report no.: Monatshefte fur Chemie
Abstract: A series of functionalized 3-(substituted amino)thieno[2,3-b]pyridines bearing azidoacetamide and monothiooxamide fragments have been prepared starting from readily available 2-chloro-N-(thieno[2,3-b]pyridine-3-yl)acetamides. Some of the compounds proved to be strong herbicide antidotes. The key structures were confirmed by X-ray diffraction and 2D NMR techniques
URI: http://hdl.handle.net/20.500.12258/8428
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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