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Reactions of polyfluorochalcones with o- and p-phenylenediamines. Synthesis and intramolecular transformations of polyfluorinated 2,4-diaryl-2,3-dihydrobenzo-1H-1,5-diazepines Full article

Journal Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Output data Year: 2015, Volume: 51, Number: 2, Pages: 253-260 Pages count : 8 DOI: 10.1134/S1070428015020207
Authors Borodina E.A. 1 , Orlova N.A. 1
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

Abstract: Polyfluorochalcones react with o-phenylenediamine in ethanol and 2-propanol in the presence of triethylamine or benzyltriethylammonium chloride (TEBAC) affording polyfluorinated 2,4-diaryl-2,3-dihydrobenzo-1H-1,5-diazepines. Along with the latter in the presence of triethylamine Michael aza-adducts presumably formed, and at the use of TEBAC in 2-propanol products of intramolecular cyclization and rearrangement of benzo-1,5-diazepines, dihydrobenzimidazo[1,2-a]quinolines were obtained. The reactions of polyfluorochalcones with p-phenylenediamine in ethanol or DMF proceed mostly with the substitution of the para-fluorine atom in the perfluorophenyl rings.
Cite: Borodina E.A. , Orlova N.A.
Reactions of polyfluorochalcones with o- and p-phenylenediamines. Synthesis and intramolecular transformations of polyfluorinated 2,4-diaryl-2,3-dihydrobenzo-1H-1,5-diazepines
Russian Journal of Organic Chemistry. 2015. V.51. N2. P.253-260. DOI: 10.1134/S1070428015020207 WOS Scopus РИНЦ OpenAlex
Original: Соболева Е.А. , Орлова Н.А.
Взаимодействие полифторхалконов с о- и n-фенилендиаминами. синтез и внутримолекулярные превращения полифторзамещенных 2,4-диарил-2,3-дигидробензо-1н-1,5-диазепинов
Журнал органической химии (RUSS J ORG CHEM+). 2015. Т.51. №2. С.263-270. РИНЦ
Dates:
Published print: Feb 1, 2015
Published online: Mar 26, 2015
Identifiers:
Web of science: WOS:000351844300020
Scopus: 2-s2.0-84925847489
Elibrary: 24020247
OpenAlex: W2016692954
Citing:
DB Citing
Web of science 3
Scopus 3
Elibrary 3
OpenAlex 3
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