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Enantioselective Michael Reaction of Malonates to Nitroolefins Catalyzed by Bifunctional Organocatalysts
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Citations
23
References
2003
Year
Chiral Bifunctional OrganocatalystsNovel OrganocatalystsEngineeringTertiary Amino GroupBiochemistryBifunctional OrganocatalystsNatural SciencesMichael AdductsOrganic ChemistryCatalysisNitroolefins CatalyzedChemistryStereoselective SynthesisAsymmetric CatalysisEnantioselective Michael ReactionEnantioselective SynthesisBiomolecular Engineering
Michael reaction of malonates to nitroolefins with chiral bifunctional organocatalysts, bearing both a thiourea and tertiary amino group, afforded Michael adducts with high yields and enantioselectivities (up to 95%, up to 93% ee).
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