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Organocatalyzed Regio- and Enantioselective Allylic Trifluoromethylation of Morita–Baylis–Hillman Adducts Using Ruppert–Prakash Reagent
113
Citations
41
References
2011
Year
Asymmetric CatalysisChemical EngineeringEnantioselective Allylic TrifluoromethylationEngineeringCross-coupling ReactionEnantioselective SynthesisBis-cinchona Alkaloid CatalystOrganic ChemistryCatalysisChemistryHalogenationRuppert-prakash ReagentSynthetic ChemistryAsymmetric Allylic TrifluoromethylationBiomolecular Engineering
The organocatalyzed regioselective allylic trifluoromethylation of Morita-Baylis-Hillman adducts using Ruppert-Prakash reagent was achieved in high to excellent yields via a successive S(N)2'/S(N)2' mode for the first time. The reaction was extended to the asymmetric allylic trifluoromethylation by the use of a bis-cinchona alkaloid catalyst with high enantioselectivities up to 94% ee.
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