Publication | Open Access
Copper‐Catalyzed Enantioselective 1,6‐Boration of <i>para</i>‐Quinone Methides and Efficient Transformation of <i>gem</i>‐Diarylmethine Boronates to Triarylmethanes
278
Citations
103
References
2015
Year
Para-quinone MethidesChemical EngineeringEfficient TransformationEngineeringExcellent EnantioselectivitiesDerived PotassiumOrganic ChemistryOrganometallic CatalysisCatalysisChemistryCopper‐catalyzed Enantioselective 1,6‐BorationAsymmetric CatalysisSynthetic ChemistryEnantioselective Synthesis
Presented is the first enantioselective copper-catalyzed 1,6-conjugate addition of bis(pinacolato)diboron to para-quinone methides. The reaction proceeds with excellent yields and good to excellent enantioselectivities, and provides an attractive approach to the construction of optically active gem-diarylmehtine boronic esters. Additionally, the subsequent conversion of the derived potassium trifluoroborates into triarylmethanes with highly enantiospecificity was realized.
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