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Chemo- and Stereoselective C-H Oxidations and Epoxidations/cis-Dihydroxylations with H2O2, Catalyzed by Non-Heme Iron and Manganese Complexes Обзор

Журнал Coordination Chemistry Reviews
ISSN: 0010-8545 , E-ISSN: 1873-3840
Вых. Данные Год: 2012, Том: 256, Номер: 13-14, Страницы: 1418-1434 Страниц : 17 DOI: 10.1016/j.ccr.2012.04.005
Ключевые слова Active sites, Asymmetric, Epoxidation, Hydrocarbons, Hydrogen peroxide, Iron, Manganese, Mechanism, Non-heme, Oxidation
Авторы Talsi Evgenii P. 1 , Bryliakov Konstantin P. 1
Организации
1 Boreskov Institute of Catalysis, Pr. Lavrentieva 5, Novosibirsk 630090, Russian Federation

Информация о финансировании (1)

1 Российский фонд фундаментальных исследований 12-03-00782

Реферат: The discovery of simple and efficient catalyst systems for the selective oxofunctionalization of hydrocarbons is a challenging task of modern chemistry. The biomimetic approach, which aims at mimicking the reactivity of natural enzymes in catalyzed transformation with synthetic low-molecular weight compounds, has been widely applied to the search for new transition metal based catalyst systems in the last two decades. In effect, numerous iron and manganese complexes modeling the catalytic performance of non-heme metal-containing monooxygenases have been reported and intensively investigated. In this contribution, non-heme iron- and manganese catalyzed selective oxidations of alkanes, as well as chemo- and stereoselective epoxidations and cis-dihydroxylations of alkenes, using H2O2 as the oxygen source, are reviewed, with major focus on the their synthetic potential. Recent experimental investigations of the nature of catalytically active species and mechanisms of their action are summarized.
Библиографическая ссылка: Talsi E.P. , Bryliakov K.P.
Chemo- and Stereoselective C-H Oxidations and Epoxidations/cis-Dihydroxylations with H2O2, Catalyzed by Non-Heme Iron and Manganese Complexes
Coordination Chemistry Reviews. 2012. V.256. N13-14. P.1418-1434. DOI: 10.1016/j.ccr.2012.04.005 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 7 февр. 2012 г.
Принята к публикации: 3 апр. 2012 г.
Опубликована online: 11 апр. 2012 г.
Опубликована в печати: 1 июл. 2012 г.
Идентификаторы БД:
Web of science: WOS:000305037200005
Scopus: 2-s2.0-84860888705
РИНЦ: 17985138
Chemical Abstracts: 2012:612541
Chemical Abstracts (print): 157:548033
OpenAlex: W2062482634
Цитирование в БД:
БД Цитирований
Web of science 332
Scopus 353
РИНЦ 343
OpenAlex 361
Альметрики: