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Enantioselective organocatalytic phospha-Michael reaction of α,β-unsaturated aldehydes
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Citations
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References
2011
Year
Diaryl Phosphine OxidesChemical EngineeringNovel OrganocatalystsEngineering1,4-Addition Adductsβ-Unsaturated AldehydesOrganic ChemistryCatalysisStereoselective SynthesisChemistryAsymmetric CatalysisEnantioselective Synthesis
The enantioselective organocatalytic phospha-Michael reaction of α,β-unsaturated aldehydes with diaryl phosphine oxides is explored for the first time using (S)-2-(diphenyl(trimethylsilyloxy)methyl)pyrrolidine as a catalyst. It afforded 1,4-addition adducts in good to excellent yields with up to 99% ee.
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