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Asymmetric Autoamplification in the Oxidative Kinetic Resolution of Secondary Benzylic Alcohols Catalyzed by Manganese Complexes Научная публикация

Журнал ChemCatChem
ISSN: 1867-3880 , E-ISSN: 1867-3899
Вых. Данные Год: 2017, Том: 9, Страницы: 2599 -2607 Страниц : 9 DOI: 10.1002/cctc.201700438
Ключевые слова asymmetric autoamplification, hydrogen peroxide, kinetic resolution, manganese, oxidation
Авторы Talsi Evgenii P. 1,2 , Samsonenko Denis G. 1,3 , Bryliakov Konstantin P. 1,2
Организации
1 Novosibirsk State University, Pirogova 2, Novosibirsk 630090 (Russian Federation)
2 Boreskov Institute of Catalysis, Pr. Lavrentieva 5, Novosibirsk 630090 (Russian Federation)
3 Nikolaev Institute of Inorganic Chemistry, Pr. Lavrentieva 3, Novosibirsk 630090 (Russian Federation)

Информация о финансировании (1)

1 Российский научный фонд 17-13-01117

Реферат: Herein, chiral Mn–aminopyridine complexes have been shown to catalyze the oxidation of alkylarenes to enantiomerically enriched 1-arylalkanols with hydrogen peroxide. The observed enantiomeric excess values result from the direct enantioselective benzylic C−H hydroxylation, accompanied by stereoconvergent oxidative kinetic resolution of the resulting alcohol. Testing several (S,S)-bipyrrolidine derived Mn complexes has revealed a novel catalyst (6) that exhibits the best kinetic resolution in the series (krel up to 8.8), along with sufficient reactivity and efficiency (>1000 catalytic turnovers). The mechanistic study of the Mn-mediated alcohol oxidation witnesses electrophilic active species (ρ=−1.2), with rate-limiting H abstraction (kH/kD=2.2), followed by oxygen rebound and dehydration of the resulting gem-diol to form the ketone. Intriguingly, while for the resolution of the relatively bulky 1,2-diphenylethanol, krel is virtually constant throughout the reaction, for less bulky alcohols, krel increases with increasing conversion, in line with the rising optical purity of the 1-arylalkanol. The latter participates in the oxidation as an auxiliary ligand, assisting the chiral recognition. This effect is related to the previously described asymmetric autocatalysis and asymmetric autoinduction, but is not identical with either of those, with the differences being discussed. To unambiguously identify this effect, the term asymmetric autoamplification (chiral autoamplification) is proposed.
Библиографическая ссылка: Talsi E.P. , Samsonenko D.G. , Bryliakov K.P.
Asymmetric Autoamplification in the Oxidative Kinetic Resolution of Secondary Benzylic Alcohols Catalyzed by Manganese Complexes
ChemCatChem. 2017. V.9. P.2599 -2607. DOI: 10.1002/cctc.201700438 WOS Scopus РИНЦ CAPlus OpenAlex
Даты:
Поступила в редакцию: 13 мар. 2017 г.
Опубликована online: 21 мар. 2017 г.
Опубликована в печати: 7 июл. 2017 г.
Идентификаторы БД:
Web of science: WOS:000405457300022
Scopus: 2-s2.0-85020407379
РИНЦ: 31016582
Chemical Abstracts: 2017:963113
OpenAlex: W2597749866
Цитирование в БД:
БД Цитирований
Web of science 38
Scopus 37
РИНЦ 37
OpenAlex 39
Альметрики: