Publication | Closed Access
Scalable Electrochemical Transition‐Metal‐Free Dehydrogenative Cross‐Coupling Amination Enabled Alkaloid Clausines Synthesis
53
Citations
49
References
2020
Year
EngineeringPrivileged Carbazole MoietyOrganometallic ElectrochemistryOrganic ChemistryChemistryChemical EngineeringOrganic ElectrochemistryOrganometallic CatalysisStereoselective SynthesisRadical Reaction PathwayMolecular ElectrochemistryDiversity-oriented SynthesisCatalysisEnantioselective SynthesisBiomolecular EngineeringNatural SciencesElectrosynthesisSynthetic ChemistrySustainable Nature
Abstract Reported herein is an environmentally benign electrochemical C−H bond dehydrogenative amination protocol for the construction of privileged carbazole moiety with broad generality. Preliminary mechanistic investigations implied a radical reaction pathway. Compared with traditional ionic routes, the scalable transition‐metal and exogenous‐oxidant free strategy highlighted the green and sustainable nature of this method. magnified image
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