Organic Letters · 2003 · 144 citations · 10 references
EngineeringOrganic ChemistryChemistryBipi LigandsFacial SelectivityOrganometallic CatalysisStereoselective SynthesisInorganic ChemistryPhysicsQuantum ChemistryAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringNatural SciencesNew Bipi LigandsPhosphine Electron DensityMolecular ComplexAsymmetric Heck ReactionElectronic Effects
[structure: see text] The new BIPI ligands are phosphinoimidazolines that can be electronically tuned in three different ligand regions to explore electronic effects in asymmetric catalysis. Their application to the asymmetric Heck reaction (AHR) in the creation of a chiral quaternary center is described. Enantioselectivity is shown for the first time to depend linearly on phosphine electron density. Changing the ligand basicity by variation of the R(2) or R(3) substituents reverses facial selectivity.
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Tsuneo Imamoto, Toshiyuki Oshiki, Takashi Onozawa et al. · Journal of the American Chemical Society · 1990 · 421 citations
Inorganic Chemistry, Homochiral Phosphine Centers, Engineering +12
Atsuyuki Ashimori, Benoit Bachand, Larry E. Overman et al. · Journal of the American Chemical Society · 1998 · 235 citations
Asymmetric Catalysis, Halogenation, Catalytic Asymmetric Synthesis +15
Atsuyuki Ashimori, Benoit Bachand, Michael A. Calter et al. · Journal of the American Chemical Society · 1998 · 183 citations
Catalytic Asymmetric Synthesis, Monomeric Pd−binap, Engineering +17