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dc.contributor.authorФізер, Максим Михайлович-
dc.contributor.authorСливка, Михайло Васильович-
dc.contributor.authorБаумер, Вячеслав М.-
dc.contributor.authorЛендєл, Василь Георгійович-
dc.date.accessioned2015-11-27T10:27:26Z-
dc.date.available2015-11-27T10:27:26Z-
dc.date.issued2015-11-13-
dc.identifier.citationMaksym M. Fizer, Mikhailo V. Slivka*, Vjacheslav M. Baumer, Vasil G. Lendel. Specificity of Alkylation of 5-R-Amino-4-aroyl-1,2,4-triazole-3-thione. // Chemistry of Nitrogen Containing Heterocycles, CNCH-2015, 19th - 13th November, 2015, Kharkiv, Ukraine. Book of Abstracts. – Kharkiv: Ekskluziv Publ., 2015. – 124 p.uk
dc.identifier.isbn978-966-2166-81-1-
dc.identifier.urihttps://dspace.uzhnu.edu.ua/jspui/handle/lib/4968-
dc.descriptionDepartment of Organic Chemistry, Faculty of Chemistry, Uzhhorod National University, Fedinca str. 53/1, Uzhhorod, 88000, Ukraine, e-mail: [email protected]uk
dc.description.abstractIt was investigated the alkylation reaction of 5-R-amino-4-aroyl-1,2,4-triazole-3-thiones. Initial triazoles had been received after heating of aroyl-bis-thoureas in n-butanol or acetonitrile medium up to full releasing of hydrogen sulfide. Alkylation was carried out in alcoholic medium at base presence. It was shown, that Dimroth rearrangement with 1,3,4-thiadiazole ring formation is realized under above mentioned conditions.uk
dc.language.isoenuk
dc.publisherKharkiv: Ekskluziv Publ. [email protected]uk
dc.relation.ispartofseriesТези конференції;2015-11-
dc.subjectПерегрупування Дімротаuk
dc.subject1,2,4-triazole, 1,3,4-thiadiazole, Dimroth rearrangement, alkylation.uk
dc.titleSpecificity of Alkylation of 5-R-Amino-4-aroyl-1,2,4-triazole-3-thioneuk
dc.title.alternativeСпецифіка алкілування 5-аміно-4-ароїл-1,2,4-триазол-3-тіонуuk
dc.typeTextuk
dc.pubTypeТези до статтіuk
Appears in Collections:Наукові публікації кафедри органічної хімії

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