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Asymmetric Epoxidation of Olefins with Sodium Percarbonate Catalyzed by Bis-amino-bis-pyridine Manganese Complexes Full article

Journal Molecules
ISSN: 1420-3049
Output data Year: 2022, Volume: 27, Number: 8, Article number : 2538, Pages count : 7 DOI: 10.3390/molecules27082538
Tags enantioselective; epoxidation; manganese; sodium percarbonate; olefin; alkene
Authors Drozd Varvara A. 1 , Ottenbacher Roman V. 1 , Bryliakov Konstantin P. 1
Affiliations
1 Boreskov Institute of Catalysis, Pr. Lavrentieva 5, 630090 Novosibirsk, Russia

Funding (1)

1 Ministry of Science and Higher Education of the Russian Federation 0239-2021-0009

Abstract: Asymmetric epoxidation of a series of olefinic substrates with sodium percarbonate oxidant in the presence of homogeneous catalysts based on Mn complexes with bis-amino-bis-pyridine ligands is reported. Sodium percarbonate is a readily available and environmentally benign oxidant that is studied in these reactions for the first time. The epoxidation proceeded with good to high yields (up to 100%) and high enantioselectivities (up to 99% ee) using as low as 0.2 mol. % catalyst loadings. The epoxidation protocol is suitable for various types of substrates, including unfunctionalized alkenes, α,β-unsaturated ketones, esters (cis- and trans-), and amides (cis- and trans-). The reaction mechanism is discussed.
Cite: Drozd V.A. , Ottenbacher R.V. , Bryliakov K.P.
Asymmetric Epoxidation of Olefins with Sodium Percarbonate Catalyzed by Bis-amino-bis-pyridine Manganese Complexes
Molecules. 2022. V.27. N8. 2538 :1-7. DOI: 10.3390/molecules27082538 WOS Scopus РИНЦ AN PMID OpenAlex
Dates:
Submitted: Mar 25, 2022
Accepted: Apr 12, 2022
Published print: Apr 14, 2022
Published online: Apr 14, 2022
Identifiers:
Web of science: WOS:000787431600001
Scopus: 2-s2.0-85128802378
Elibrary: 48432373
Chemical Abstracts: 2022:1140307
PMID: 35458734
OpenAlex: W4224223197
Citing:
DB Citing
Scopus 7
Elibrary 6
Web of science 7
OpenAlex 8
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