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dc.contributor.authorФізер, Максим Михайлович-
dc.contributor.authorСливка, Михайло Васильович-
dc.contributor.authorБаумер, Вячеслав-
dc.contributor.authorЛендєл, Василь Георгійович-
dc.identifier.citationMaksym Fizer, Mikhailo Slivka*, Vjacheslav Baumer, Vasil Lendel. Synthesis of 3-alkyl-5-allylamino-2-benzoylimino-1,3,4-thiadiazoles via Dimroth rearrangement. // Heterocyclic Communications. 2016, Volume 22, Issue 2, Pages 79–83. ISSN (Online) 2191-0197, ISSN (Print) 0793-0283, on-line: DOI: 10.1515/hc-2015-0279, March
dc.identifier.issnISSN (Print) 0793-0283-
dc.descriptionCorresponding author: Mikhailo Slivka, Organic Synthesis Laboratory, Uzhhorod National University, Uzhhorod 88000, Ukraine, e-mail: [email protected]uk
dc.description.abstractA facile access to 3-alkyl-5-N-allylamino- 2-N′-benzoylimino-1,3,4-thiadiazoles via Dimroth rearrangement is reported. Alkylation of 5-allylamino- 4-benzoyl-1,2,4-triazole-3-thione with alkyl halides in basic alcohol solution is regioselective. A mechanism for the formation of a 1,3,4-thiadiazole ring by 1,2,4-triazole recyclization is proposed. The obtained compounds were characterized by NMR, elemental analysis and X-ray diffraction
dc.description.sponsorshipThis research was partly supported by the International Visegrad Fund [contract number: 51501563]uk
dc.publisherDe Gruyter
dc.relation.ispartofseriesНаукова стаття;2016-02-
dc.subjectalkylation; Dimroth rearrangement; 1,3,4-thiadiazole; 1,2,4-triazoleuk
dc.subjectIMPACT FACTOR 2014: 0.593 SCImago Journal Rank (SJR) 2014: 0.201 Source Normalized Impact per Paper (SNIP) 2014: 0.307 Impact per Publication (IPP) 2014: 0.513uk
dc.titleSynthesis of 3-alkyl-5-allylamino-2-benzoylimino-1,3,4-thiadiazoles via Dimroth
dc.title.alternativeСинтез 3-alkyl-5-allylamino-2-benzoylimino-1,3,4-thiadiazoles перегрупуванням Дімрота.uk
Appears in Collections:Наукові публікації кафедри органічної хімії

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