Publication | Closed Access
Chiral Calix[4]arenes-Bearing Prolinamide Functionality as Organocatalyst for Asymmetric Direct Aldol Reactions in Water
14
Citations
39
References
2016
Year
Novel OrganocatalystsEngineeringChiral CalixOrganic ChemistryL-prolinamido GroupCatalysisHigh YieldChemistryStereoselective SynthesisNatural Product SynthesisAsymmetric CatalysisEnantioselective SynthesisBiomolecular Engineering
The chiral calix[4]arene derivative (6) bearing an L-prolinamido group has been designed and proved to be a water compatible efficient organocatalysts for a direct enantioselective aldol reaction. Compound 6 catalyzes the aldol reaction of cyclohexanone and a variety of aromatic aldehydes yielding anti-aldol products in high yield with enantioselectivities of up to 93% and diastereoselectivity of up to 95:5.
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