- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
-
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)
- Creator
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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
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:55 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
- Laglera‐Gándara, Carlos J.
- Jiménez‐Pérez, Julián
- Fernández‐de‐Córdova, Francisco J.
- Ríos, Pablo
- Conejero, Salvador
Other Objects (12)
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
Three‐Component Aminoarylation of Electron‐Rich Alkenes by Merging Photoredox with Nickel Catalysis
A Catalytic Three‐Component Aminofluorination of Unactivated Alkenes with Electron‐Rich Amino Sources
Transfer hydrosilylation
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
Three‐Component Aminoarylation of Electron‐Rich Alkenes by Merging Photoredox with Nickel Catalysis
A Catalytic Three‐Component Aminofluorination of Unactivated Alkenes with Electron‐Rich Amino Sources
Transfer hydrosilylation
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
Three‐Component Aminoarylation of Electron‐Rich Alkenes by Merging Photoredox with Nickel Catalysis
A Catalytic Three‐Component Aminofluorination of Unactivated Alkenes with Electron‐Rich Amino Sources
Transfer hydrosilylation