Publication | Closed Access
(IPr)Pd(acac)Cl: An Easily Synthesized, Efficient, and Versatile Precatalyst for C−N and C−C Bond Formation
188
Citations
7
References
2006
Year
Chemical EngineeringCross-coupling ReactionAlpha-ketone Arylation ReactionsC−c Bond FormationEngineeringEasily SynthesizedNovel OrganocatalystsCatalytic SynthesisOrganic ChemistryVersatile PrecatalystActive Pdii PrecatalystCatalysisSynthetic ChemistryChemistryOrganometallic CatalysisHeterocyclic Aryl ChloridesBiomolecular Engineering
A very straightforward synthesis of (IPr)Pd(acac)Cl from two commercially available starting materials, Pd(acac)2 and IPr.HCl [acac = acetylacetonate; IPr = N,N'-bis(2,6-diisopropylphenyl)imidazol-2-ylidene], has been developed. The resulting complex, (IPr)Pd(acac)Cl (1), has proven to be a highly active PdII precatalyst in the Buchwald-Hartwig and the alpha-ketone arylation reactions. A wide range of substrates has been screened, including unactivated, sterically hindered, and heterocyclic aryl chlorides.
| Year | Citations | |
|---|---|---|
Page 1
Page 1