Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/8428
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dc.contributor.authorDotsenko, V. V.-
dc.contributor.authorДоценко, В. В.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenova, I. V.-
dc.contributor.authorАксенова, И. В.-
dc.date.accessioned2019-11-18T12:26:58Z-
dc.date.available2019-11-18T12:26:58Z-
dc.date.issued2019-
dc.identifier.citationDotsenko, 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 1973-1985ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/8428-
dc.description.abstractA 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 techniquesru
dc.language.isoenru
dc.publisherSpringer-Verlag Wienru
dc.relation.ispartofseriesMonatshefte fur Chemie-
dc.subjectMonothiooxamidesru
dc.subjectHeterocyclesru
dc.subjectAcylationru
dc.subjectAzidoacetamidesru
dc.subjectBiological activityru
dc.subjectCombinatorial chemistryru
dc.titleSubstituted N-(thieno[2,3-b]pyridine-3-yl)acetamides: synthesis, reactions, and biological activityru
dc.typeСтатьяru
vkr.amountPages 1973-1985ru
vkr.instИнститут математики и естественных наук-
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