Transformations of 1-(2-Aminophenyl)propan-2-ol to 2-Methylindoline Научная публикация
Журнал |
Catalysis Letters
ISSN: 1011-372X , E-ISSN: 1572-879X |
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Вых. Данные | Год: 2015, Том: 145, Страницы: 955-963 Страниц : 9 DOI: 10.1007/s10562-014-1474-3 | ||||||||||
Ключевые слова | Acidity, Alcohols, Amines, Zeolites | ||||||||||
Авторы |
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Организации |
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Информация о финансировании (2)
1 | European Commission | 246095 FP7-NMP-2009-LARGE-3 POLYCAT |
2 | Åbo Akademi University |
Реферат:
The transformation reaction of 1-(2-aminophenyl)propan-2-ol was studied at 200 C under argon pressure. A range of catalysts was applied including carbon, titania and zeolite supported Ru, Pd, Pt, Rh, and Ir, as well as metal free zeolites. The highest conversion was obtained with H-Beta-150 and H-Beta-25 and the highest selectivity to
2-methylindoline was achieved with 0.3 % Ir–H-Beta-150 and H-Beta-25. Although the selectivity to 2-methylindole was high for all catalysts, formation of the final product 2-methylindoline only took place over the most acidic catalysts.
Библиографическая ссылка:
Bernas H.
, Demidova Y.S.
, Aho A.
, Simakova I.L.
, Kumar N.
, Laribi Y.
, Perrichon P.
, Leino R.
, Murzin D.Y.
Transformations of 1-(2-Aminophenyl)propan-2-ol to 2-Methylindoline
Catalysis Letters. 2015. V.145. P.955-963. DOI: 10.1007/s10562-014-1474-3 WOS Scopus РИНЦ
Transformations of 1-(2-Aminophenyl)propan-2-ol to 2-Methylindoline
Catalysis Letters. 2015. V.145. P.955-963. DOI: 10.1007/s10562-014-1474-3 WOS Scopus РИНЦ
Даты:
Поступила в редакцию: | 21 нояб. 2014 г. |
Принята к публикации: | 29 дек. 2014 г. |
Опубликована online: | 10 янв. 2015 г. |
Опубликована в печати: | 1 мар. 2015 г. |
Идентификаторы БД:
Web of science | WOS:000350677000026 |
Scopus | 2-s2.0-84938394654 |
РИНЦ | 23995566 |
Chemical Abstracts | 2015:67471 |
Chemical Abstracts (print) | 162:326791 |
OpenAlex | W2080908063 |