Superacid Catalyzed Reactions of 5-Amino-1-Naphthol with Benzene and Cyclohexane Научная публикация
Журнал |
Tetrahedron
ISSN: 0040-4020 , E-ISSN: 1464-5416 |
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Вых. Данные | Год: 2002, Том: 58, Номер: 27, Страницы: 5423-5426 Страниц : 4 DOI: 10.1016/S0040-4020(02)00512-4 | ||
Ключевые слова | Aminonaphthol, Condensation, Ionic hydrogenation, Superacid, Superelectrophile | ||
Авторы |
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Организации |
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Реферат:
5-Amino-1-naphthol undergoes ionic hydrogenation with cyclohexane and condenses with benzene when reacted in the presence of excess of aluminum halides to give 5-amino-1-tetralone (10) and 5-amino-3-phenyl-1-tetralone, respectively. In CF3SO3H as well as CF3SO3H–SbF5 superacidic media 5-amino-1-naphthol gave N,C-diprotonated dication that can be considered as the superelectrophilic intermediate in the reactions with cyclohexane and benzene. The mechanism of these reactions is discussed.
Библиографическая ссылка:
Koltunov K.Y.
, Prakash G.K.S.
, Rasul G.
, Olah G.A.
Superacid Catalyzed Reactions of 5-Amino-1-Naphthol with Benzene and Cyclohexane
Tetrahedron. 2002. V.58. N27. P.5423-5426. DOI: 10.1016/S0040-4020(02)00512-4 WOS Scopus РИНЦ
Superacid Catalyzed Reactions of 5-Amino-1-Naphthol with Benzene and Cyclohexane
Tetrahedron. 2002. V.58. N27. P.5423-5426. DOI: 10.1016/S0040-4020(02)00512-4 WOS Scopus РИНЦ
Даты:
Поступила в редакцию: | 12 апр. 2002 г. |
Принята к публикации: | 16 мая 2002 г. |
Опубликована online: | 29 мая 2002 г. |
Опубликована в печати: | 1 июл. 2002 г. |
Идентификаторы БД:
Web of science | WOS:000176653300004 |
Scopus | 2-s2.0-0036642742 |
РИНЦ | 14258991 |
Chemical Abstracts | 2002:483379 |
Chemical Abstracts (print) | 137:384629 |
OpenAlex | W2047375407 |