Mn Catalyzed Bioinspired Oxidation of Aliphatic C-H Groups: Chemo-, Regio-, Stereoselectivity, and Mechanism Доклады на конференциях
Язык | Английский | ||||
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Тип доклада | Ключевой | ||||
Конференция |
XXII International Symposium on Homogeneous Catalysis 24-29 июл. 2022 , Lisbon |
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Авторы |
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Организации |
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Реферат:
Herewith, our recent results in the chemo-, regio-, and stereoselective catalytic oxygenation of C(sp3)-H groups with hydrogen peroxide in the presence Mn complexes with bis-imino-bis-pyridylmethyl and related N4-donor ligands are summarized. Under optimal conditions, secondary and tertiary C-H groups can be hydroxylated in good to high yields, chemo-, and stereoselectivities (up to 97 % ee). The use of “polarity reversal” approach for the suppression of overoxidation of methylene groups to carbonyl groups is exemplified for enantioselective benzylic C-H hydroxylations.
Библиографическая ссылка:
Ottenbacher R.V.
, Bryliakova A.A.
, Kurganskii V.I.
, Bryliakov K.P.
Mn Catalyzed Bioinspired Oxidation of Aliphatic C-H Groups: Chemo-, Regio-, Stereoselectivity, and Mechanism
XXII International Symposium on Homogeneous Catalysis 24-29 Jul 2022
Mn Catalyzed Bioinspired Oxidation of Aliphatic C-H Groups: Chemo-, Regio-, Stereoselectivity, and Mechanism
XXII International Symposium on Homogeneous Catalysis 24-29 Jul 2022