Publication | Closed Access
Direct Arylation of α‐Amino C(sp<sup>3</sup>)‐H Bonds by Convergent Paired Electrolysis
31
Citations
59
References
2019
Year
EngineeringOrganometallic ElectrochemistryOrganic ChemistryChemistryElectrolysis MethodChemical EngineeringOrganic ElectrochemistryElectrolysis StrategyConvergent Paired ElectrolysisCross-coupling ReactionBiochemistryDiversity-oriented SynthesisCatalysisElectrochemistryBiomolecular EngineeringNatural SciencesElectrosynthesisPeptide SynthesisBenzonitrile Derivatives
Abstract A metal‐free convergent paired electrolysis strategy to synthesize benzylic amines through direct arylation of tertiary amines and benzonitrile derivatives at room temperature has been developed. This TEMPO‐mediated electrocatalytic reaction makes full use of both anodic oxidation and cathodic reduction without metals or stoichiometric oxidants, thus showing great potential and advantages for practical synthesis. This convergent paired electrolysis method provides a straightforward and powerful means to activate C−H bonds and realize cross‐coupling with cathodically generated species.
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