Enantiocomplementary Epoxidation Reactions Catalyzed by an Engineered Cofactor‐Independent Non‐natural Peroxygenase
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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Enantiocomplementary Epoxidation Reactions Catalyzed by an Engineered Cofactor‐Independent Non‐natural Peroxygenase ; volume:59 ; number:26 ; year:2020 ; pages:10374-10378 ; extent:5
Angewandte Chemie / International edition. International edition ; 59, Heft 26 (2020), 10374-10378 (gesamt 5)
- Creator
- DOI
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10.1002/anie.202001373
- URN
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urn:nbn:de:101:1-2022061213030319475142
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:25 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Xu, Guangcai
- Crotti, Michele
- Saravanan, Thangavelu
- Kataja, Kim M.
- Poelarends, Gerrit
Other Objects (12)
Enantiocomplementary Epoxidation Reactions Catalyzed by an Engineered Cofactor‐Independent Non‐natural Peroxygenase
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Dendritic Fluoroalcohols Catalyzed Alkene Epoxidation with H2O2
Regioselective hydration of terpenoids using cofactor-independent hydratases
Iron‐Catalyzed Epoxidation of Linear α‐Olefins with Hydrogen Peroxide
Vanadium-catalyzed epoxidation reaction of cinnamyl alcohol in ionic liquids
Cofactor-independent C–C bond cleavage reactions catalyzed by the AlpJ family of oxygenases in atypical angucycline biosynthesis
Precisely Engineered Supported Gold Clusters as a Stable Catalyst for Propylene Epoxidation
Precisely Engineered Supported Gold Clusters as a Stable Catalyst for Propylene Epoxidation
Ti-catalyzed asymmetric epoxidation of terminal, non-conjugated olefins with hydrogen peroxide
Asymmetric bio-epoxidation catalyzed with the styrene monooxygenase from Pseudomonas sp. LQ26
Enantiocomplementary Epoxidation Reactions Catalyzed by an Engineered Cofactor‐Independent Non‐natural Peroxygenase
Peptide-Catalyzed Asymmetric Epoxidation
Manganese-Catalyzed Enantioselective Alkene Epoxidation
Dendritic Fluoroalcohols Catalyzed Alkene Epoxidation with H2O2
Regioselective hydration of terpenoids using cofactor-independent hydratases
Iron‐Catalyzed Epoxidation of Linear α‐Olefins with Hydrogen Peroxide
Vanadium-catalyzed epoxidation reaction of cinnamyl alcohol in ionic liquids
Cofactor-independent C–C bond cleavage reactions catalyzed by the AlpJ family of oxygenases in atypical angucycline biosynthesis
Precisely Engineered Supported Gold Clusters as a Stable Catalyst for Propylene Epoxidation
Precisely Engineered Supported Gold Clusters as a Stable Catalyst for Propylene Epoxidation
Ti-catalyzed asymmetric epoxidation of terminal, non-conjugated olefins with hydrogen peroxide
Asymmetric bio-epoxidation catalyzed with the styrene monooxygenase from Pseudomonas sp. LQ26
Enantiocomplementary Epoxidation Reactions Catalyzed by an Engineered Cofactor‐Independent Non‐natural Peroxygenase
Peptide-Catalyzed Asymmetric Epoxidation
Manganese-Catalyzed Enantioselective Alkene Epoxidation
Dendritic Fluoroalcohols Catalyzed Alkene Epoxidation with H2O2
Regioselective hydration of terpenoids using cofactor-independent hydratases
Iron‐Catalyzed Epoxidation of Linear α‐Olefins with Hydrogen Peroxide
Vanadium-catalyzed epoxidation reaction of cinnamyl alcohol in ionic liquids
Cofactor-independent C–C bond cleavage reactions catalyzed by the AlpJ family of oxygenases in atypical angucycline biosynthesis
Precisely Engineered Supported Gold Clusters as a Stable Catalyst for Propylene Epoxidation
Precisely Engineered Supported Gold Clusters as a Stable Catalyst for Propylene Epoxidation
Ti-catalyzed asymmetric epoxidation of terminal, non-conjugated olefins with hydrogen peroxide