SYNTHESIS OF 1,2,4-TRIAZOLO[1,5-<i>a</i>]PYRIMIDINE SYSTEM

Авторы

  • Maksym M. Fizer Faculty of Chemistry, Uzhhorod National University, 46 Pidhirna St., Uzhhorod 88000
  • Mikhailo V. Slivka Ужгородский национальный университет

DOI:

https://doi.org/10.1007/2876

Ключевые слова:

essramycin, [1, 2, 4]triazolo[1, 5-a]pyrimidines, Biginelli reaction

Аннотация

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.

How to Cite
Fizer, M.; Slivka, M. Chem. Heterocycl. Compd. 2016, 52, 155. [Khim. Geterotsikl. Soedin. 2016, 52, 155.]

For this article in the English edition see DOI 10.1007/s10593-016-1851-5

Биографии авторов

Maksym M. Fizer, Faculty of Chemistry, Uzhhorod National University, 46 Pidhirna St., Uzhhorod 88000

Maksym Mikhailovich Fizer

Lector, Organic Chemistry Department, Chemical Faculty

Mikhailo V. Slivka, Ужгородский национальный университет

доцент кафедры органической химии

Загрузки

Опубликован

2016-04-11

Выпуск

Том 52 № 3 (2016)

Раздел

Гетероциклы в фокусе