Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/14692
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dc.contributor.authorAbaev, V. T.-
dc.contributor.authorАбаев, В. Т.-
dc.date.accessioned2020-12-16T13:12:05Z-
dc.date.available2020-12-16T13:12:05Z-
dc.date.issued2020-
dc.identifier.citationSerdyuk, O.V., Hampel, F., Abaev, V.T. Synthesis of isoxazolylvinyl ketones from substituted furans // Chemistry of Heterocyclic Compounds. - 2020. - Volume 56. - Issue 11. - Pages 1477–1484ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/14692-
dc.description.abstractA new method for the preparation of isoxazolylvinyl ketones related to potential cytotoxic agents has been developed. In the first step, the reaction of furfuryl ketones with hydroxylamine hydrochloride affords the corresponding oximes. Further, the oxidative ring opening – ring closure reaction of oximes leads to isoxazoles with an α, β-unsaturated carbonyl motif. The developed procedure is metal-free and does not require expensive starting materialsru
dc.language.isoenru
dc.publisherSpringerru
dc.relation.ispartofseriesChemistry of Heterocyclic Compounds-
dc.subjectChalconeru
dc.subjectFuranru
dc.subjectIsoxazoleru
dc.subjectRing opening – ring closure reactionru
dc.titleSynthesis of isoxazolylvinyl ketones from substituted furansru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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