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Asymmetric construction of trifluoromethylated pyrrolidines via Cu(i)-catalyzed 1,3-dipolar cycloaddition of azomethine ylides with 4,4,4-trifluorocrotonates
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Citations
10
References
2011
Year
First TimeEnantioselective SynthesisEngineeringHeterocyclicTrifluoromethylated Pyrrolidines1,3-Dipolar CycloadditionOrganic ChemistryOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryHeterocycle ChemistryAsymmetric ConstructionAsymmetric CatalysisExcellent StereoselectivityBiomolecular Engineering
Trifluoromethylated pyrrolidines have been synthesized via catalytic asymmetric 1,3-dipolar cycloaddition with excellent stereoselectivity for the first time. Epimerization of the endo-pyrrolidines obtained from cis-4,4,4-trifluorocrotonate into the exo-pyrrolidines was also revealed.
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