Publication | Closed Access
Catalytic Asymmetric Synthesis of Tertiary Alcohols and Oxetenes Bearing a Difluoromethyl Group
44
Citations
56
References
2015
Year
Catalytic Asymmetric SynthesisEngineeringOrganic ChemistryChemistryOxetenes BearingHigh YieldsChemical EngineeringSolvent-free ConditionsOrganometallic CatalysisHomogeneous CatalysisDiversity-oriented SynthesisCatalysisAsymmetric CatalysisEnantioselective SynthesisCatalytic SynthesisDicationic Palladium ComplexBiomolecular EngineeringAlkene MetathesisNatural SciencesTertiary Alcohols
The catalytic asymmetric ene reaction with difluoropyruvate as an electrophile in the presence of a dicationic palladium complex is shown. This is the reliable and practical catalytic asymmetric synthesis for various α-CF2H tertiary alcohols in high yields and enantioselectivities. The reaction with isobutene can be catalyzed efficiently under solvent-free conditions with low catalyst loading (up to S/C 2000). Furthermore, difluoropyruvate is applicable to the [2 + 2] cycloaddition reaction in high yields and enantioselectivities.
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