Publication | Closed Access
P-chirogenic organocatalysts: application to the aza-Morita–Baylis–Hillman (aza-MBH) reaction of ketimines
81
Citations
37
References
2013
Year
High YieldsP-chirogenic OrganocatalystsChemical EngineeringNovel OrganocatalystsEngineeringNatural SciencesDiversity-oriented SynthesisOrganic ChemistryAcyclic α-Keto EstersCatalysisChemistryAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
The P-chirogenic organocatalysts were found to promote the enantioselective aza-Morita-Baylis-Hillman reaction of ketimines derived from acyclic α-keto esters. In the P-chirogenic organocatalyzed aza-MBH reactions, α,α-disubstituted α-amino acid derivatives were obtained in high yields with high enantioselectivities (up to 97% ee).
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