Synthesis of 3-alkyl-5-allylamino-2-benzoylimino-1,3,4-thiadiazoles via Dimroth rearrangement.

Фізер, Максим Михайлович; Сливка, Михайло Васильович; Баумер, Вячеслав; Лендєл, Василь Георгійович

Please use this identifier to cite or link to this item: https://dspace.uzhnu.edu.ua/jspui/handle/lib/9065

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DC Field	Value	Language
dc.contributor.author	Фізер, Максим Михайлович	-
dc.contributor.author	Сливка, Михайло Васильович	-
dc.contributor.author	Баумер, Вячеслав	-
dc.contributor.author	Лендєл, Василь Георгійович	-
dc.date.accessioned	2016-07-02T09:39:55Z	-
dc.date.available	2016-07-02T09:39:55Z	-
dc.date.issued	2016-03-12	-
dc.identifier.citation	Maksym 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 2016.	uk
dc.identifier.issn	ISSN (Print) 0793-0283	-
dc.identifier.uri	https://dspace.uzhnu.edu.ua/jspui/handle/lib/9065	-
dc.description	Corresponding author: Mikhailo Slivka, Organic Synthesis Laboratory, Uzhhorod National University, Uzhhorod 88000, Ukraine, e-mail: [email protected]	uk
dc.description.abstract	A 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 analysis.	uk
dc.description.sponsorship	This research was partly supported by the International Visegrad Fund [contract number: 51501563]	uk
dc.language.iso	en	uk
dc.publisher	De Gruyter Publ.	uk
dc.relation.ispartofseries	Наукова стаття;2016-02	-
dc.subject	alkylation; Dimroth rearrangement; 1,3,4-thiadiazole; 1,2,4-triazole	uk
dc.subject	IMPACT 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: 0.513	uk
dc.title	Synthesis of 3-alkyl-5-allylamino-2-benzoylimino-1,3,4-thiadiazoles via Dimroth rearrangement.	uk
dc.title.alternative	Синтез 3-alkyl-5-allylamino-2-benzoylimino-1,3,4-thiadiazoles перегрупуванням Дімрота.	uk
dc.type	Text	uk
dc.pubType	Стаття	uk
Appears in Collections:	Наукові публікації кафедри органічної хімії

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