Publication | Closed Access
Probing Electronic Effects in the Asymmetric Heck Reaction with the BIPI Ligands
144
Citations
10
References
2003
Year
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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1990 | 421 | |
1998 | 235 | |
1998 | 183 | |
2002 | 174 | |
1997 | 143 | |
1993 | 103 | |
1992 | 91 | |
1969 | 45 | |
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