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Pd(II)-Catalyzed Enantioselective C–H Activation of Cyclopropanes
403
Citations
33
References
2011
Year
Medicinal ChemistryNovel OrganocatalystsEngineeringBiochemistryNatural SciencesSystematic Ligand DevelopmentOrganic ChemistryOrganometallic CatalysisCatalysisEnantioselective C–h ActivationChemistryOrganoboron ReagentsStereoselective SynthesisAsymmetric CatalysisEnantioselective SynthesisNew Retrosynthetic Disconnection
Systematic ligand development has led to the identification of novel mono-N-protected amino acid ligands for Pd(II)-catalyzed enantioselective C-H activation of cyclopropanes. A diverse range of organoboron reagents can be used as coupling partners, and the reaction proceeds under mild conditions. These results provide a new retrosynthetic disconnection for the construction of enantioenriched cis-substituted cyclopropanecarboxylic acids.
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