Publication | Closed Access
[Bmim]PF<sub>6</sub>-Promoted Ligandless Suzuki–Miyaura Coupling Reaction of Potassium Aryltrifluoroborates in Water
38
Citations
68
References
2014
Year
Inorganic ChemistryChemical EngineeringCross-coupling ReactionEngineeringBiochemistryNatural SciencesFluorous SynthesisCatalytic SystemOrganic ChemistrySuzuki-miyaura Coupling ReactionsCatalysisChemistryPotassium AryltrifluoroboratesSynthetic Chemistry
The Suzuki-Miyaura coupling reactions of potassium aryltrifluoroborates with aryl bromides in water are promoted by the addition of [bmim]PF6 using Pd(OAc)2 as a catalyst and Na2CO3 as a base under air. The quantity of [bmim]PF6 used is crucial to the efficiency of the catalytic system. A wide range of biaryls and polyaryls can be easily prepared in good to excellent yields.
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