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DC Field | Value | Language |
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dc.contributor.author | Фізер, Максим Михайлович | - |
dc.contributor.author | Сливка, Михайло Васильович | - |
dc.date.accessioned | 2016-07-02T09:55:01Z | - |
dc.date.available | 2016-07-02T09:55:01Z | - |
dc.date.issued | 2016-03-12 | - |
dc.identifier.citation | Maksym 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: http://hgs.osi.lv/index.php/hgs/issue/view/104 | uk |
dc.identifier.uri | https://dspace.uzhnu.edu.ua/jspui/handle/lib/9066 | - |
dc.description | Corresponding author: Mikhailo Slivka, Organic Synthesis Laboratory, Uzhhorod National University, Uzhhorod 88000, Ukraine, e-mail: [email protected] | uk |
dc.description.abstract | In 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]pyrimidines. | uk |
dc.description.sponsorship | УжНУ | uk |
dc.language.iso | en | uk |
dc.publisher | Elsevier | uk |
dc.relation.ispartofseries | Наукова стаття;2016-03 | - |
dc.subject | essramycin; [1,2,4]triazolo[1,5-a]pyrimidines; Biginelli reaction | uk |
dc.title | Synthesis of [1,2,4]triazolo[1,5-a]pyrimidine (microreview). | uk |
dc.title.alternative | Synthesis of [1,2,4]triazolo[1,5-a]pyrimidine. | uk |
dc.type | Text | uk |
dc.pubType | Стаття | uk |
Appears in Collections: | Наукові публікації кафедри органічної хімії |
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Synthesis of [1,2,4]triazolo[1,5-a]pyrimidine (microreview) - Springer.html | 172.02 kB | HTML | View/Open |
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