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Title: [1,3]Thiazolo[2′,3′:3,4][1,2,4]triazolo[1,5-a]pyrimidines – A New Heterocyclic System Accessed via Bromocyclization
Other Titles: [1,3]Тіазоло[2′,3′:3,4][1,2,4]триазоло[1,5-a]піримідини – нова гетероциклічна система, отримана бромогетероциклізацією
Authors: Фізер, Максим Михайлович
Сливка, Михайло Васильович
Русанов, Едуард
Туров, Олександр
Лендєл, Василь Георгійович
Keywords: [1,3]Thiazolo[2′,3′:3,4][1,2,4]triazolo[1,5-a]pyrimidines – A New Heterocyclic System Accessed via Bromocyclization
Issue Date: 15-May-2015
Publisher: Wiley Online Library
Citation: Maksym Fizer, Mikhailo Slivka, Eduard Rusanov, Alexandr Turov and Vasil Lendel. [1,3]Thiazolo[2′,3′:3,4][1,2,4]triazolo[1,5-a]pyrimidines – A New Heterocyclic System Accessed via Bromocyclization. // Journal of Heterocyclic Chemistry. Volume 52, Issue 3, pages 949–952, May 2015. Impact Factor (2014): 0.787 (Web of Science, Scopus). SNIP (2014) 0.50
Series/Report no.: Наукова стаття;2015-17
Abstract: A facile access to novel condensed system of [1,3]thiazolo[2′,3′:3,4][1,2,4]triazolo[1,5-a]pyrimidine is presented. This protocol consists of bromine-assisted direct electrophilic heterocyclization of 3-N-allylamine-5,6-dihydro[1,3]thiazolo[2,3-c][1,2,4]triazole. The bromination took place in acetic acid and gave a good yield of the target product, which was dehydrobrominated by sodium acetate action.
Description: Мikhailo Slivka, Department of Organic Chemistry, Faculty of Chemistry, Uzhgorod National University, Fedinets 53/1, Uzhgorod, Ukraine *E-mail: [email protected]
Type: Text
Publication type: Стаття
ISSN: Online ISSN: 1943-5193
Appears in Collections:Наукові публікації кафедри органічної хімії

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