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Access to Functionalized Quinones via the Aromatic Oxidation of Phenols Bearing an Alcohol or Olefinic Function Catalyzed by Supported Iron Phthalocyanine Научная публикация

Журнал New Journal of Chemistry
ISSN: 1144-0546 , E-ISSN: 1369-9261
Вых. Данные Год: 2006, Том: 30, Номер: 12, Страницы: 1768-1773 Страниц : 6 DOI: 10.1039/b608834a
Ключевые слова HYPERVALENT IODINE REAGENTS; HETEROGENEOUS OXIDATION; SELECTIVE OXIDATIONS; ORGANIC-SYNTHESIS; COMPLEXES; SILICAS; SULFONAMIDES; ALLYLATION; TI-MMM-2; ROUTE
Авторы Zalomaeva Olga V. 1,2 , Sorokin Alexander B. 1
Организации
1 Institut de Recherches sur la Catalyse, 2 av. A. Einstein, Villeurbanne, France
2 Boreskov Institute of Catalysis, 5 Ac. Lavrentiev Ave., Novosibirsk, 630090, Russia

Реферат: The controlled oxidation at only one position of compounds with several oxidizable sites, while keeping the other sites intact, has been demonstrated for phenols bearing alcohol or olefinic functional groups. Iron tetrasulfophthalocyanine supported on silica was found to be an efficient catalyst for the preparation of functionalized quinones under mild conditions, with tert-butylhydroperoxide as the oxidant. A novel rapid and mild one-pot procedure for the covalent grafting of iron tetrasulfophthalocyanine onto silica has been developed. The supported catalyst was characterized by chemical analysis, a specific surface study, UV-vis spectroscopy and XPS. A non-radical mechanism for this unusual selective oxidation has been revealed by 18O labelling experiments.
Библиографическая ссылка: Zalomaeva O.V. , Sorokin A.B.
Access to Functionalized Quinones via the Aromatic Oxidation of Phenols Bearing an Alcohol or Olefinic Function Catalyzed by Supported Iron Phthalocyanine
New Journal of Chemistry. 2006. V.30. N12. P.1768-1773. DOI: 10.1039/b608834a WOS Scopus РИНЦ OpenAlex CAPlusCA
Даты:
Поступила в редакцию: 21 июн. 2006 г.
Принята к публикации: 30 авг. 2006 г.
Опубликована online: 26 сент. 2006 г.
Опубликована в печати: 1 дек. 2006 г.
Идентификаторы БД:
≡ Web of science: WOS:000243194000024
≡ Scopus: 2-s2.0-33846255430
≡ РИНЦ: 13520669
≡ OpenAlex: W1987791592
≡ Chemical Abstracts: 2007:16008
≡ Chemical Abstracts (print): 146:274039
Цитирование в БД:
≡ Web of science 43 Сбор данных от 13.02.2026
≡ Scopus 45 Сбор данных от 15.02.2026
≡ РИНЦ 42 Сбор данных от 15.02.2026
≡ OpenAlex 39 Сбор данных от 15.02.2026
Альметрики: