Peculiarities of 4-methallyl-5-methallylamino- 1,2,4-triazole-3-thione halogenation

Please use this identifier to cite or link to this item: https://dspace.uzhnu.edu.ua/jspui/handle/lib/26202

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DC Field	Value	Language
dc.contributor.author	Fizer, Maksym M.	-
dc.contributor.author	Slivka, Mikhailo V.	-
dc.contributor.author	Lendel, Vasil G.	-
dc.date.accessioned	2019-10-18T12:09:19Z	-
dc.date.available	2019-10-18T12:09:19Z	-
dc.date.issued	2019-04	-
dc.identifier.citation	Maksym M. Fizer, Mikhailo V. Slivka, Vasil G. Lendel. Peculiarities of 4-methallyl-5-methallylamino- 1,2,4-triazole-3-thione halogenation. // Chemistry of Heterocyclic Compounds 2019, 55(4/5), 478–480	uk
dc.identifier.uri	https://dspace.uzhnu.edu.ua/jspui/handle/lib/26202	-
dc.description.abstract	Bromination and iodination of 4-methallyl-5-methallylamino-1,2,4-triazole-3-thione lead to the annulation of five- and six-membered thiazaheterocycles, respectively. The usage of halogen excess does not give the product of 5-methallylamino group cyclization – the product of the bromine addition was isolated	uk
dc.language.iso	en	uk
dc.relation.ispartofseries	2019_01;	-
dc.subject	[1,3]thiazolo[2,3-c][1,2,4]triazole, 1,2,4-triazole, [1,2,4]triazolo[3,4-b][1,3]thiazine, electrophilic cyclization, halogenation	uk
dc.title	Peculiarities of 4-methallyl-5-methallylamino- 1,2,4-triazole-3-thione halogenation	uk
dc.title.alternative	Особливості галогенування 4-металіл-5-металіламіно-1,2,4-триазол-3-тіону	uk
dc.type	Text	uk
dc.pubType	Стаття	uk
Appears in Collections:	Наукові публікації кафедри органічної хімії

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