Publication | Closed Access
Chelation‐Assisted Palladium‐Catalyzed γ‐Arylation of Aliphatic Carboxylic Acid Derivatives
67
Citations
66
References
2017
Year
γ ‐C–h ArylationCross-coupling ReactionFunctional Group ToleranceAliphatic Carboxylic AcidEngineeringPalladium‐catalyzed γ‐ArylationOrganic ChemistryOrganometallic CatalysisCatalysisChemistryAsymmetric CatalysisBiomolecular Engineering
Abstract A palladium(II)‐catalyzed protocol for the highly regioselective remote γ ‐C–H arylation of aliphatic carboxylic acid has been disclosed. The 8‐aminoquinoline moiety as an intramolecular bidentate chelator was found to be suitable for this γ ‐C–H arylation. Various aryl iodides successfully produced the regioselectively mono‐arylated products with negligible diarylation. Functional group tolerance and easy‐to‐handle reaction conditions make this method attractive. magnified image
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