Publication | Open Access
Nickel-Catalyzed Kumada Cross-Coupling Reactions of Tertiary Alkylmagnesium Halides and Aryl Bromides/Triflates
181
Citations
28
References
2011
Year
Chemical EngineeringCross-coupling ReactionEngineeringAryl Bromides/triflatesTertiary Alkyl NucleophilesTertiary Alkylmagnesium HalidesElectrosynthesisAryl TriflatesOrganic ChemistryNi-catalyzed ProcessCatalysisOrganometallic CatalysisChemistryHalogenationAsymmetric CatalysisBiomolecular Engineering
We report a Ni-catalyzed process for the cross-coupling of tertiary alkyl nucleophiles and aryl bromides. This process is extremely general for a wide range of electrophiles and generally occurs with a ratio of retention to isomerization >30:1. The same procedure also accommodates the use of aryl triflates, vinyl chlorides, and vinyl bromides as the electrophilic component.
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