Publication | Closed Access
Asymmetric Synthesis of Monodentate Phosphine Ligands Based on Chiral η<sup>6</sup>-Cr[arene] Templates
52
Citations
7
References
1999
Year
Asymmetric CatalysisInorganic ChemistryCross-coupling ReactionEngineeringMonodentate Phosphine LigandsAsymmetric SynthesisActive Cr-complexed ArylphosphinesOrganic ChemistryOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryChiral PhosphinePhosphine LigandsSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
Optically active Cr-complexed arylphosphines are presented as a new class of chiral monodentate phosphine ligand for use in asymmetric catalysis. Asymmetric synthesis of the chiral phosphine ligands 9 is achieved in three steps from the achiral Cr[arene] precursor 3. A variety of ligand structures are accessed from a common synthesis intermediate. The utility of these phosphine ligands in asymmetric catalysis is highlighted in Pd(II)-catalyzed allylic alkylation reactions.
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