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Polyfluorinated 2,4-diaryl-2,3-dihydro-1H-1,5-benzodiazepines: Synthesis and new rearrangement into polyfluorodihydrobenzimidazo[1,2-a]quinolines Научная публикация

Журнал Journal of Fluorine Chemistry
ISSN: 0022-1139
Вых. Данные Год: 2014, Том: 162, Страницы: 66-70 Страниц : 5 DOI: 10.1016/j.jfluchem.2014.03.013
Ключевые слова Polyfluorochalcones; Polyfluorinated 2,4-diaryl-2,3-dihydrobenzo-1H-1,5-diazepines; Polyfluorinated dihydrobenzimidazo[1,2-a]quinolines; Intramolecular fluorine substitution; Rearrangement
Авторы Borodina Elena A. 1 , Orlova Natalia A. 1 , Kargapolova Irina Yu. 1 , Gatilov Yury V. 1
Организации
1 (Данные Web of science) NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

Реферат: Interaction of polyfluorinated chalcones (pentafluorobenzalacetophenone, benzalpentafluoroacetophenone and decafluorochalcone) with 1,2-diaminobenzene in alcohols in the presence of triethylamine or quaternary ammonium salt (TEBAC) has been investigated. In the presence of TEBAC in 2-propanol polyfluorinated 2,4-diaryl-2,3-dihydro-1H-1,5-benzodiazepines are formed. Some of them undergo intramolecular fluorine substitution and unusual rearrangement into a previously unknown polyfluoro-containing tetracyclic compounds-(6aR)-1,2,3,4-tetrafluoro-6a-aryl-6a,7-dihydrobenzimidazo[1,2-a]quinolines, under the reaction conditions as well as in absence of TEBAC. The structures are established on NMR spectra and confirmed by X-ray. (C) 2014 Elsevier B.V. All rights reserved.
Библиографическая ссылка: Borodina E.A. , Orlova N.A. , Kargapolova I.Y. , Gatilov Y.V.
Polyfluorinated 2,4-diaryl-2,3-dihydro-1H-1,5-benzodiazepines: Synthesis and new rearrangement into polyfluorodihydrobenzimidazo[1,2-a]quinolines
Journal of Fluorine Chemistry. 2014. V.162. P.66-70. DOI: 10.1016/j.jfluchem.2014.03.013 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 июн. 2014 г.
Идентификаторы БД:
Web of science: WOS:000336827000009
Scopus: 2-s2.0-84899538076
РИНЦ: 21874107
OpenAlex: W2062305257
Цитирование в БД:
БД Цитирований
Web of science 5
Scopus 5
РИНЦ 4
OpenAlex 5
Альметрики: