Publication | Closed Access
Organocatalytic Vinyl Azide‐Carbonyl [3+2] Cycloaddition: High‐Yielding Synthesis of Fully Decorated <i>N</i>‐Vinyl‐1,2,3‐Triazoles
45
Citations
73
References
2016
Year
Asymmetric CatalysisNovel OrganocatalystsOrganocatalytic Vinyl Azide‐carbonylCatalyst SimplicityEngineeringVast ApplicationsVinyl AzidesOrganic ChemistryCatalysisStereoselective SynthesisChemistryHeterocycle ChemistryHigh‐yielding SynthesisEnantioselective SynthesisBiomolecular Engineering
Abstract For the first time, an enolate‐mediated organocatalytic vinyl azide‐carbonyl [3+2] cycloaddition (OrgVACC) of various ketones/aldehydes with vinyl azides is reported. It is an efficient intermolecular reaction with excellent outcomes with reference to rate, yield, selectivity, operational simplicity, substrate scope, catalyst simplicity, and vast applications.
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