Electrophilic Hydrosilylation of Electron‐Rich Alkenes Derived from Enamines
- 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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Electrophilic Hydrosilylation of Electron‐Rich Alkenes Derived from Enamines ; day:27 ; month:05 ; year:2024 ; extent:12
Angewandte Chemie / International edition. International edition ; (27.05.2024) (gesamt 12)
- Urheber
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Laglera‐Gándara, Carlos J.
Jiménez‐Pérez, Julián
Fernández‐de‐Córdova, Francisco J.
Ríos, Pablo
Conejero, Salvador
- DOI
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10.1002/anie.202404859
- URN
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urn:nbn:de:101:1-2405271413486.063027661788
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 10:55 MESZ
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Beteiligte
- Laglera‐Gándara, Carlos J.
- Jiménez‐Pérez, Julián
- Fernández‐de‐Córdova, Francisco J.
- Ríos, Pablo
- Conejero, Salvador
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B(C6F5)3-Catalyzed Transfer Hydrosilylation of Alkenes
Hydrosilylation of Alkenes Catalyzed by Platinum on N-Doped Graphene
Copper-catalyzed trifluoromethylation of alkenes with an electrophilic trifluoromethylating reagent
Electrochemical Vicinal Difluorination of Alkenes: Scalable and Amenable to Electron‐Rich Substrates †
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Electrophilic Fluorination of Alkenes via Bora‐Wagner–Meerwein Rearrangement. Access to β‐Difluoroalkyl Boronates
Electrophilic Hydrosilylation of Electron‐Rich Alkenes Derived from Enamines
Oxidative dimerization of electron rich alkenes
B(C6F5)3-Catalyzed Transfer Hydrosilylation of Alkenes
Hydrosilylation of Alkenes Catalyzed by Platinum on N-Doped Graphene
Copper-catalyzed trifluoromethylation of alkenes with an electrophilic trifluoromethylating reagent
Electrochemical Vicinal Difluorination of Alkenes: Scalable and Amenable to Electron‐Rich Substrates †
Electrochemical Vicinal Difluorination of Alkenes: Scalable and Amenable to Electron‐Rich Substrates †
Three‐Component Aminoarylation of Electron‐Rich Alkenes by Merging Photoredox with Nickel Catalysis
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