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Perfluoro(5-aza-4-nonene) in the synthesis of heterocyclic compounds containing a perfluoropropyl group Full article

Journal Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Output data Year: 2000, Volume: 36, Number: 1, Pages: 109-116 Pages count : 8
Authors Furin G.G. 1 , Kiriyanko V.G. 1 , Lopyrev V.A. 2 , Zhuzhgov E.L. 3 , Protsuk N.I. 2
Affiliations
1 (Scopus) Novosibirsk Inst. of Organ. Chem., Siberian Division, Russian Academy of Sciences, pr. Akademika Lavrent'eva 9, Novosibirsk, 630090, Russian Federation
2 (Scopus) Irkutsk Institute of Chemistry, Siberian Division, Russian Academy of Sciences, ul. Favorskogo 1, Irkutsk, 664033, Russian Federation
3 (Scopus) Novosibirsk State University, ul. Pirogova 2, Novosibirsk, 630090, Russian Federation

Abstract: Reactions of perfluoro(5-aza-4-nonene) with isopropylamine, tert-butylamine, 2-amino-6-bromo-benzothiazole, and 2-amino-1-methylbenzimidazole in THF in the presence of triethylamine gave the corresponding diazetine derivatives. Reactions of the title compound with difunctional reagents, such as benzamidine, acetamidine, phenylhydrazine, pentafluorophenylhydrazine, and heprafluorobutyrohydrazide, resulted in formation of 1,3,5-triazine and 1,2,4-triazole derivatives. Possible reaction pathways, the role of triethylamine, and spectral parameters of the products are discussed. * This study was financially supported by the Russian Foundation for Basic Research (project no. 96-03-33047).
Cite: Furin G.G. , Kiriyanko V.G. , Lopyrev V.A. , Zhuzhgov E.L. , Protsuk N.I.
Perfluoro(5-aza-4-nonene) in the synthesis of heterocyclic compounds containing a perfluoropropyl group
Russian Journal of Organic Chemistry. 2000. V.36. N1. P.109-116. Scopus РИНЦ
Original: Furin G.G. , Kiriyanko V.G. , Lopyrev V.A. , Zhuzhgov E.L. , Protsuk N.I.
Application of perfluoro-5-aza-4-nonene in the synthesis of certain heterocyclic compounds, containing perfluoropropyl group
Журнал органической химии (RUSS J ORG CHEM+). 2000. V.36. N1. P.120-127. WOS
Identifiers:
Scopus: 2-s2.0-0033633867
Elibrary: 13344922
Citing:
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Elibrary 5