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Copper(II)-Catalyzed Enantioselective Intramolecular Cyclization of <i>N</i>-Alkenylureas
67
Citations
41
References
2015
Year
Novel OrganocatalystsEngineeringCyclic Vicinal DiaminesOrganic ChemistryEnantioselective Intramolecular CyclizationCarbonyl GroupCatalysisStereoselective SynthesisChemistryHeterocycle ChemistryFirst CuOrganometallic CatalysisAsymmetric CatalysisEnantioselective SynthesisBiomolecular Engineering
The first Cu(II)-catalyzed highly enantioselective intramolecular cyclization of N-alkenylureas was developed for the concise assembly of chiral vicinal diamino bicyclic heterocycles. Facile removal of carbonyl group of the carbamido moiety allowed for ready access to enantioenriched cyclic vicinal diamines.
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