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dc.contributor.authorФізер, Максим Михайлович-
dc.contributor.authorСливка, Михайло Васильович-
dc.identifier.citationMaksym Fizer, Mikhailo Slivka*. Synthesis of [1,2,4]triazolo[1,5-a]pyrimidine (microreview). // Chemistry of Heterocyclic Compounds, Volume 52, Issue 3, Pages 155–157. on-line:
dc.descriptionCorresponding author: Mikhailo Slivka, Organic Synthesis Laboratory, Uzhhorod National University, Uzhhorod 88000, Ukraine, e-mail: [email protected]uk
dc.description.abstractIn this review article we have focused on synthetic approaches for the creation of [1,2,4]triazolo[1,5-a]pyrimidine system. The synthetic ways for the preparation of [1,2,4]triazolo[1,5-a]pyrimidines can be divided into two main groups: annulation of pyrimidine moiety to triazole ring and annulation of triazole fragment to pyrimidine ring. The Dimroth rearrangement of [1,2,4]triazolo[4,3-a]pyrimidines can also be used for the synthesis of [1,2,4]triazolo[1,5-a]
dc.relation.ispartofseriesНаукова стаття;2016-03-
dc.subjectessramycin; [1,2,4]triazolo[1,5-a]pyrimidines; Biginelli reactionuk
dc.titleSynthesis of [1,2,4]triazolo[1,5-a]pyrimidine (microreview).uk
dc.title.alternativeSynthesis of [1,2,4]triazolo[1,5-a]
Appears in Collections:Наукові публікації кафедри органічної хімії

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