Reactions of 5-, 6-, 7-, 8-Hydroxyquinolines and 5-Hydroxyisoquinoline with Benzene and Cyclohexane in Superacids Научная публикация
Журнал |
Journal of Organic Chemistry
ISSN: 0022-3263 , E-ISSN: 1520-6904 |
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Вых. Данные | Год: 2002, Том: 67, Номер: 12, Страницы: 4330-4336 Страниц : 7 DOI: 10.1021/jo020099n | ||
Ключевые слова | Aluminum; Chlorine; Hydrogenation; Ionic conduction | ||
Авторы |
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Организации |
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Реферат:
Isomeric 5-, 6-, 7-hydroxyquinolines (11−13) and 5-hydroxyisoquinoline (14) gave N,C-diprotonated dications in CF3SO3H−SbF5 superacid medium. Compounds 11, 13, 14, and 8-hydroxyquinoline (5) underwent selective ionic hydrogenation with cyclohexane in the presence of aluminum chloride. Compounds 11 and 14 condense with benzene in the presence of aluminum halides. The detailed mechanism of reactions, which involves superelectrophilic dicationic intermediates, is discussed.
Библиографическая ссылка:
Koltunov K.Y.
, Prakash G.K.S.
, Rasul G.
, Olah G.A.
Reactions of 5-, 6-, 7-, 8-Hydroxyquinolines and 5-Hydroxyisoquinoline with Benzene and Cyclohexane in Superacids
Journal of Organic Chemistry. 2002. V.67. N12. P.4330-4336. DOI: 10.1021/jo020099n WOS Scopus РИНЦ
Reactions of 5-, 6-, 7-, 8-Hydroxyquinolines and 5-Hydroxyisoquinoline with Benzene and Cyclohexane in Superacids
Journal of Organic Chemistry. 2002. V.67. N12. P.4330-4336. DOI: 10.1021/jo020099n WOS Scopus РИНЦ
Даты:
Поступила в редакцию: | 11 февр. 2002 г. |
Опубликована online: | 11 мая 2002 г. |
Опубликована в печати: | 1 июн. 2002 г. |
Идентификаторы БД:
Web of science | WOS:000176173700043 |
Scopus | 2-s2.0-0037077012 |
РИНЦ | 14258993 |
Chemical Abstracts | 2002:354572 |
Chemical Abstracts (print) | 137:93497 |
OpenAlex | W1972826787 |