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Chiral Manganese Aminopyridine Complexes: the Versatile Catalysts of Chemo- and Stereoselective Oxidations with H2O2 Научная публикация

Журнал Chemical Record
ISSN: 1527-8999 , E-ISSN: 1528-0691
Вых. Данные Год: 2018, Том: 18, Номер: 1, Страницы: 78-90 Страниц : 13 DOI: 10.1002/tcr.201700032
Ключевые слова asymmetric epoxidation, C−H oxidation, hydrogen peroxide, manganese, mechanism
Авторы Ottenbacher Roman V. 1,2 , Talsi Evgenii P. 1,2 , Bryliakov Konstantin P. 1,2
Организации
1 Chemistry Department, Novosibirsk State University, Pirogova 2, Novosibirsk 630090 (Russia)
2 Boreskov Institute of Catalysis, Pr. Lavrentieva 5, Novosibirsk 630090 (Russia)

Информация о финансировании (2)

1 Российский научный фонд 17-13-01117
2 Российский фонд фундаментальных исследований 16-33-00014

Реферат: In the last decade, manganese(II) complexes with N-donor tetradentate aminopyridine ligands emerged as efficient catalysts of enantioselective epoxidation of olefins and direct selective oxidation of C−H groups in complex organic molecules, with environmentally benign oxidant hydrogen peroxide. In this personal account, we summarize the progress of these catalysts with regard to ligands design, structure-reactivity correlations, evaluation of the substrate scope, as well as mechanistic studies, shedding light on the nature of active sites and the mechanisms of selective oxygenations. Several practically promising catalytic syntheses with the aid of Mn aminopyridine catalysts are exemplified.
Библиографическая ссылка: Ottenbacher R.V. , Talsi E.P. , Bryliakov K.P.
Chiral Manganese Aminopyridine Complexes: the Versatile Catalysts of Chemo- and Stereoselective Oxidations with H2O2
Chemical Record. 2018. V.18. N1. P.78-90. DOI: 10.1002/tcr.201700032 WOS Scopus РИНЦ CAPlus PMID OpenAlex
Даты:
Поступила в редакцию: 10 мая 2017 г.
Опубликована online: 14 июл. 2017 г.
Опубликована в печати: 1 янв. 2018 г.
Идентификаторы БД:
Web of science: WOS:000419935300007
Scopus: 2-s2.0-85025171244
РИНЦ: 35513224
Chemical Abstracts: 2017:1176039
PMID (PubMed): 28707370
OpenAlex: W2734658276
Цитирование в БД:
БД Цитирований
Web of science 47
Scopus 50
РИНЦ 43
OpenAlex 51
Альметрики: