Hemilabile and Redox‐Active Quinone Ligands Unlock sp 3 ‐Rich Couplings in Nickel‐Catalyzed Olefin Carbosulfenylation
- 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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Hemilabile and Redox‐Active Quinone Ligands Unlock sp 3 ‐Rich Couplings in Nickel‐Catalyzed Olefin Carbosulfenylation ; day:07 ; month:11 ; year:2024 ; extent:12
Angewandte Chemie / International edition. International edition ; (07.11.2024) (gesamt 12)
- Creator
- DOI
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10.1002/anie.202411870
- URN
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urn:nbn:de:101:1-2411081348198.254566740853
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:35 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
- Li, Zi‐Qi
- Alturaifi, Turki M.
- Cao, Yilin
- Joannou, Matthew V.
- Liu, Peng
- Engle, Keary
Other Objects (12)
Hemilabile and Redox‐Active Quinone Ligands Unlock sp 3 ‐Rich Couplings in Nickel‐Catalyzed Olefin Carbosulfenylation
Nickel-catalyzed cross-couplings involving strong bond activation
Nickel-catalyzed Suzuki–Miyaura cross-couplings of aldehydes
Oxygen‐Stable Electrochemical CO 2 Capture using Redox‐Active Heterocyclic Benzodithiophene Quinone
Oxygen‐Stable Electrochemical CO 2 Capture using Redox‐Active Heterocyclic Benzodithiophene Quinone
Development of nickel-catalyzed decarbonylative couplings via unreactive bond activations
The First Use of Aryltrimethylammonium Salts in Nickel-Catalyzed Suzuki Cross-Couplings
Annulation of a 1,3-dithiole ring to a sterically hindered o-quinone core. Novel ditopic redox-active ligands
Air-Stable Secondary Phosphine Oxides for Nickel-Catalyzed Cross-Couplings of Aryl Ethers by C–O Activation
Quinone binding site in a type VI sulfide:quinone oxidoreductase
Latest Developments on Palladium- and Nickel-Catalyzed Cross-Couplings Using Aryl Chlorides: Suzuki–Miyaura and Buchwald–Hartwig Reactions
Nickel-Catalyzed Heck Reaction
Hemilabile and Redox‐Active Quinone Ligands Unlock sp 3 ‐Rich Couplings in Nickel‐Catalyzed Olefin Carbosulfenylation
Nickel-catalyzed cross-couplings involving strong bond activation
Nickel-catalyzed Suzuki–Miyaura cross-couplings of aldehydes
Oxygen‐Stable Electrochemical CO 2 Capture using Redox‐Active Heterocyclic Benzodithiophene Quinone
Oxygen‐Stable Electrochemical CO 2 Capture using Redox‐Active Heterocyclic Benzodithiophene Quinone
Development of nickel-catalyzed decarbonylative couplings via unreactive bond activations
The First Use of Aryltrimethylammonium Salts in Nickel-Catalyzed Suzuki Cross-Couplings
Annulation of a 1,3-dithiole ring to a sterically hindered o-quinone core. Novel ditopic redox-active ligands
Air-Stable Secondary Phosphine Oxides for Nickel-Catalyzed Cross-Couplings of Aryl Ethers by C–O Activation
Quinone binding site in a type VI sulfide:quinone oxidoreductase
Latest Developments on Palladium- and Nickel-Catalyzed Cross-Couplings Using Aryl Chlorides: Suzuki–Miyaura and Buchwald–Hartwig Reactions
Nickel-Catalyzed Heck Reaction
Hemilabile and Redox‐Active Quinone Ligands Unlock sp 3 ‐Rich Couplings in Nickel‐Catalyzed Olefin Carbosulfenylation
Nickel-catalyzed cross-couplings involving strong bond activation
Nickel-catalyzed Suzuki–Miyaura cross-couplings of aldehydes
Oxygen‐Stable Electrochemical CO 2 Capture using Redox‐Active Heterocyclic Benzodithiophene Quinone
Oxygen‐Stable Electrochemical CO 2 Capture using Redox‐Active Heterocyclic Benzodithiophene Quinone
Development of nickel-catalyzed decarbonylative couplings via unreactive bond activations
The First Use of Aryltrimethylammonium Salts in Nickel-Catalyzed Suzuki Cross-Couplings
Annulation of a 1,3-dithiole ring to a sterically hindered o-quinone core. Novel ditopic redox-active ligands
Air-Stable Secondary Phosphine Oxides for Nickel-Catalyzed Cross-Couplings of Aryl Ethers by C–O Activation
Quinone binding site in a type VI sulfide:quinone oxidoreductase
Latest Developments on Palladium- and Nickel-Catalyzed Cross-Couplings Using Aryl Chlorides: Suzuki–Miyaura and Buchwald–Hartwig Reactions