Publication | Open Access
Palladium‐Catalyzed Asymmetric Reductive Heck Reaction of Aryl Halides
168
Citations
86
References
2015
Year
Aryl HalidesCross-coupling ReactionEngineeringHigh StereoselectivityGlycol SolventOrganic ChemistryHalide DissociationOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryHalogenationAsymmetric CatalysisBiomolecular Engineering
Asymmetric reductive Heck reaction of aryl halides is realized in high stereoselectivity. Hydrogen-bond donors, trialkylammonium salts in a glycol solvent, were used to promote halide dissociation from neutral arylpalladium complexes to access cationic, stereoselective pathways.
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