Publication | Closed Access
Enantioselective Organocatalytic Addition of Azlactones to Maleimides: A Highly Stereocontrolled Entry to 2,2‐Disubstituted‐2<i>H</i>‐oxazol‐5‐ones
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Citations
55
References
2010
Year
Corresponding 2,2-Disubstituted-2h-oxazol-5-onesBifunctional Thiourea CatalystsEnantioselective Organocatalytic SynthesisNovel OrganocatalystsEngineeringNatural SciencesHighly Stereocontrolled EntryDiversity-oriented SynthesisOrganic ChemistryCatalysisEnantioselective Organocatalytic AdditionChemistryStereoselective SynthesisPharmacologyAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
The first highly diastereo- and enantioselective organocatalytic synthesis of 2,2-disubstituted-2H-oxazol-5-ones is described. The addition of oxazolones to maleimides is promoted by bifunctional thiourea catalysts, which afford the corresponding 2,2-disubstituted-2H-oxazol-5-ones with total regio- and stereocontrol.
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