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Synthesis of polyfluorinated aminoquinolines via nitroquinolines Научная публикация

Журнал Journal of Fluorine Chemistry
ISSN: 0022-1139
Вых. Данные Год: 2018, Том: 211, Страницы: 14-23 Страниц : 10 DOI: 10.1016/j.jfluchem.2018.04.006
Ключевые слова Polyfluorinated quinolines; Nitration; Reduction of nitroquinolines; Polyfluorinated aminoquinolines
Авторы Skolyapova Alexandrina D. 1 , Selivanova Galina A. 1 , Tretyakov Evgeny V. 1,2 , Bagryanskaya Irina Yu. 1,2 , Shteingarts Vitalij D. 1
Организации
1 (Данные Web of science) NN Vorozhtsov Inst Organ Chem, 9 Ac Lavrentiev Ave, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, 2 Pirogova Str, Novosibirsk 630090, Russia

Реферат: Transformation of 14 quinolines polyfluorinated in the benzene moiety was investigated in nitration systems: a mixture of HNO3 and H2SO4, NaNO3 in H2SO4, NO2BF3OH in sulfolane, or NaNO3 in oleum. 5-Nitro-and/or 8-nitro derivatives formed if positions 5 or 8 were unoccupied in the starting compounds. Otherwise, nitro products were not detectable, and the initial compounds were oxidized. In some cases, F atoms at the ortho position relative to the nitro group were substituted thus affording hydroxynitroquinolines. Polyfluorinated 2-chloroquinolines were nitrated more easily than were quinolines not containing a substituent at position 2. Thus, a method is proposed for reduction of nitroquinolines to aminoquinolines that are not available via other approaches.
Библиографическая ссылка: Skolyapova A.D. , Selivanova G.A. , Tretyakov E.V. , Bagryanskaya I.Y. , Shteingarts V.D.
Synthesis of polyfluorinated aminoquinolines via nitroquinolines
Journal of Fluorine Chemistry. 2018. V.211. P.14-23. DOI: 10.1016/j.jfluchem.2018.04.006 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 июл. 2018 г.
Идентификаторы БД:
Web of science: WOS:000435061600002
Scopus: 2-s2.0-85045573898
РИНЦ: 35491374
OpenAlex: W2797186515
Цитирование в БД:
БД Цитирований
Web of science 3
Scopus 3
РИНЦ 3
OpenAlex 3
Альметрики: