Hemilabile and Redox‐Active Quinone Ligands Unlock sp 3 ‐Rich Couplings in Nickel‐Catalyzed Olefin Carbosulfenylation
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Erschienen in
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Hemilabile and Redox‐Active Quinone Ligands Unlock sp 3 ‐Rich Couplings in Nickel‐Catalyzed Olefin Carbosulfenylation ; day:06 ; month:11 ; year:2024 ; extent:12
Angewandte Chemie ; (06.11.2024) (gesamt 12)
- Urheber
- DOI
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10.1002/ange.202411870
- URN
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urn:nbn:de:101:1-2411081321367.974896664053
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:22 MESZ
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Beteiligte
- Li, Zi‐Qi
- Alturaifi, Turki M.
- Cao, Yilin
- Joannou, Matthew V.
- Liu, Peng
- Engle, Keary
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Annulation of a 1,3-dithiole ring to a sterically hindered o-quinone core. Novel ditopic redox-active ligands
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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
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Oxygen‐Stable Electrochemical CO 2 Capture using Redox‐Active Heterocyclic Benzodithiophene Quinone
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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
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