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Transformations of 1-(2-Aminophenyl)propan-2-ol to 2-Methylindoline Научная публикация

Журнал Catalysis Letters
ISSN: 1011-372X , E-ISSN: 1572-879X
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 Bernas Heidi 1 , Demidova Yuliya S. 2,3 , Aho Atte 1 , Simakova Irina L. 2,3 , Kumar Narendra 1 , Laribi Yosra 4 , Perrichon Philippe 4 , Leino Reko 5 , Murzin Dmitry Yu. 1
Организации
1 Laboratory of Industrial Chemistry and Reaction Engineering, Process Chemistry Centre, Abo Akademi University, Biskopsgatan 8, 20500 Turku, Finland
2 Boreskov Institute of Catalysis, 630090 Novosibirsk, Russia
3 Novosibirsk State University, 630090 Novosibirsk, Russia
4 Sanofi-Aventis Recherche & Developpement, Centre de Recherche de Vitry-sur-Seine 13, Vitry-sur-Seine, France
5 Laboratory of Organic Chemistry, Abo Akademi University, Biskopsgatan 8, 20500 Turku, Finland

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 CAPlusCA OpenAlex
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
Цитирование в БД:
БД Цитирований
Web of science 2
Scopus 2
РИНЦ 2
OpenAlex 2
Альметрики: