Publication | Open Access
Nickel-Catalyzed Cross-Couplings of Benzylic Pivalates with Arylboroxines: Stereospecific Formation of Diarylalkanes and Triarylmethanes
270
Citations
40
References
2013
Year
Benzylic PivalatesChemical EngineeringStereospecific Nickel-catalyzed Cross-couplingEngineeringHeterocyclicCross-coupling ReactionOrganic ChemistryBenzylic PivalateOrganometallic CatalysisCatalysisChemistryHeterocycle ChemistryAsymmetric CatalysisStereospecific FormationNickel-catalyzed Cross-couplingsBiomolecular Engineering
We have developed a stereospecific nickel-catalyzed cross-coupling of benzylic pivalates with arylboroxines. The success of this reaction relies on the use of Ni(cod)2 as the catalyst and NaOMe as a uniquely effective base. This reaction has broad scope with respect to the arylboroxine and benzylic pivalate, enabling the synthesis of a variety of diarylalkanes and triarylmethanes in good to excellent yields and ee's.
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