Reductive Activation of Aryl Chlorides by Tuning the Radical Cation Properties of N ‐Phenylphenothiazines as Organophotoredox Catalysts
- 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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Reductive Activation of Aryl Chlorides by Tuning the Radical Cation Properties of N ‐Phenylphenothiazines as Organophotoredox Catalysts ; day:11 ; month:10 ; year:2023 ; extent:12
Chemistry - a European journal ; (11.10.2023) (gesamt 12)
- Creator
- DOI
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10.1002/chem.202302347
- URN
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urn:nbn:de:101:1-2023101215091323896827
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:48 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
- Weick, Fabian
- Hagmeyer, Nina
- Giraud, Madeleine
- Dietzek‐Ivanšić, Benjamin
- Wagenknecht, Hans-Achim
Other Objects (12)
Reductive Activation of Aryl Chlorides by Tuning the Radical Cation Properties of N ‐Phenylphenothiazines as Organophotoredox Catalysts
Nickel-on-Charcoal-Catalyzed Reductions of Aryl Chlorides
The iron-catalysed Suzuki coupling of aryl chlorides
Cross-Coupling of Secondary Alkyltrifluoroborates with Aryl Chlorides
Palladium-Catalyzed Cross-Couplings of Alkyllithiums with Aryl Chlorides
Coupling of Secondary Alkylzinc Halides with Aryl Bromides and Chlorides
Copper-Free Sonogashira Coupling of Aryl Chlorides with Pd/C
Difluoromethylation of (hetero)aryl chlorides with chlorodifluoromethane catalyzed by nickel
Amination of Aryl Chlorides via Benzynes Catalyzed by Sodium Alkoxide Clusters
Efficient Pd-catalyzed direct coupling of aryl chlorides with alkyllithium reagents
Efficient Pd‐Catalyzed Direct Coupling of Aryl Chlorides with Alkyllithium Reagents
Base‐Free Pd‐Catalyzed C−Cl Borylation of Fluorinated Aryl Chlorides
Reductive Activation of Aryl Chlorides by Tuning the Radical Cation Properties of N ‐Phenylphenothiazines as Organophotoredox Catalysts
Nickel-on-Charcoal-Catalyzed Reductions of Aryl Chlorides
The iron-catalysed Suzuki coupling of aryl chlorides
Cross-Coupling of Secondary Alkyltrifluoroborates with Aryl Chlorides
Palladium-Catalyzed Cross-Couplings of Alkyllithiums with Aryl Chlorides
Coupling of Secondary Alkylzinc Halides with Aryl Bromides and Chlorides
Copper-Free Sonogashira Coupling of Aryl Chlorides with Pd/C
Difluoromethylation of (hetero)aryl chlorides with chlorodifluoromethane catalyzed by nickel
Amination of Aryl Chlorides via Benzynes Catalyzed by Sodium Alkoxide Clusters
Efficient Pd-catalyzed direct coupling of aryl chlorides with alkyllithium reagents
Efficient Pd‐Catalyzed Direct Coupling of Aryl Chlorides with Alkyllithium Reagents
Base‐Free Pd‐Catalyzed C−Cl Borylation of Fluorinated Aryl Chlorides
Reductive Activation of Aryl Chlorides by Tuning the Radical Cation Properties of N ‐Phenylphenothiazines as Organophotoredox Catalysts
Nickel-on-Charcoal-Catalyzed Reductions of Aryl Chlorides
The iron-catalysed Suzuki coupling of aryl chlorides
Cross-Coupling of Secondary Alkyltrifluoroborates with Aryl Chlorides
Palladium-Catalyzed Cross-Couplings of Alkyllithiums with Aryl Chlorides
Coupling of Secondary Alkylzinc Halides with Aryl Bromides and Chlorides
Copper-Free Sonogashira Coupling of Aryl Chlorides with Pd/C
Difluoromethylation of (hetero)aryl chlorides with chlorodifluoromethane catalyzed by nickel
Amination of Aryl Chlorides via Benzynes Catalyzed by Sodium Alkoxide Clusters
Efficient Pd-catalyzed direct coupling of aryl chlorides with alkyllithium reagents
Efficient Pd‐Catalyzed Direct Coupling of Aryl Chlorides with Alkyllithium Reagents