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Asymmetric Suzuki–Miyaura cross-coupling of 1-bromo-2-naphthoates using the helically chiral polymer ligand PQXphos
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Citations
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References
2015
Year
Inorganic ChemistryCross-coupling ReactionEnantioselective SynthesisEngineeringSingle PqxphosAsymmetric Suzuki–miyaura Cross-couplingHelical ChiralitySolvent-dependent SwitchOrganic ChemistryCoordination PolymerChemistryAsymmetric CatalysisSynthetic ChemistryPolymer ChemistryBiomolecular EngineeringPolymers
A single-handed helical polymer ligand PQXphos afforded axially chiral biaryl esters with high enantioselectivities in asymmetric Suzuki-Miyaura cross-coupling. The use of naphthyl bromide bearing a 2,4-dimethyl-3-pentyl ester resulted in both high yields and high enantioselectivities. Either enantiomer could be synthesized selectively by using a single PQXphos through a solvent-dependent switch of the helical chirality.
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