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Highly efficient <i>ortho</i>palladated complexes of second and third benzyl amine for catalyzing the Suzuki cross‐coupling reaction
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Citations
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References
2010
Year
Inorganic ChemistryStable CatalystsCross-coupling ReactionEngineeringNatural SciencesDiversity-oriented SynthesisSuzuki Cross‐coupling ReactionThird Benzyl AmineOrganic ChemistryOrganometallic CatalysisCatalysisPhenylboronic AcidChemistryBiomolecular EngineeringAryl Bromides
Abstract In this work, ortho ‐palladated complexes [Pd(µ‐Cl)(C 6 H 4 CH 2 NRR′‐κ 2 ‐C,N)] 2 and [Pd(C 6 H 4 CH 2 NH 2 ‐2‐C,N)Cl(Y)] were tested in the Suzuki–Miyaura cross‐coupling reaction. Cyclopalladated Pd(II) complexes as thermally stable catalysts can activate aryl bromides and chlorides. These complexes were active and efficient catalysts for the Suzuki–Miyaura reaction of aryl bromides and even less reactive aryl chlorides. The cross‐coupled products of a variety of aryl bromides and aryl chloride with phenylboronic acid in methanol as solvent at 60 °C were produced in excellent yields. Copyright © 2010 John Wiley & Sons, Ltd.
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