Publication | Open Access
CuH‐Catalyzed Asymmetric Hydroamidation of Vinylarenes
99
Citations
32
References
2018
Year
Chiral AmidesEngineeringAccessible 1,4,2-Dioxazol-5-onesFunctional GroupsCuh‐catalyzed Asymmetric HydroamidationOrganic ChemistryCatalysisStereoselective SynthesisChemistryAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
A CuH-catalyzed enantioselective hydroamidation reaction of vinylarenes has been developed using readily accessible 1,4,2-dioxazol-5-ones as electrophilic amidating reagents. This method provides a straightforward and efficient approach to synthesize chiral amides in good yields with high levels of enantiopurity under mild conditions. Moreover, this transformation tolerates substrates bearing a broad range of functional groups.
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