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A new synthesis of 2-(aminoalkyl)-1,2,4-triazolo[1,5- a ]pyrimidines Научная публикация

Журнал Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436
Вых. Данные Год: 2017, Том: 27, Номер: 2, Страницы: 169-171 Страниц : 3 DOI: 10.1016/j.mencom.2017.03.021
Авторы Prezent Mikhail A. 1 , Daeva Elena D. 1 , Baranin Sergey V. 1 , Zavarzin Igor V. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

Реферат: Nickel(ii) acetylacetonate-promoted cycloaddition between Boc-protected amino acid hydrazides and benzoylcyanamide followed by deprotection gives 2-amino-5-aminoalkyl-1,2,4-triazoles, whose reaction with 1,3-dielectrophiles affords the title compounds.
Библиографическая ссылка: Prezent M.A. , Daeva E.D. , Baranin S.V. , Zavarzin I.V.
A new synthesis of 2-(aminoalkyl)-1,2,4-triazolo[1,5- a ]pyrimidines
Mendeleev Communications. 2017. V.27. N2. P.169-171. DOI: 10.1016/j.mencom.2017.03.021 WOS Scopus OpenAlex
Идентификаторы БД:
≡ Web of science: WOS:000398749600021
≡ Scopus: 2-s2.0-85016012933
≡ OpenAlex: W2600299837
Альметрики: