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Anodic Modification of Proline Derivatives Using a Lithium Perchlorate/Nitromethane Electrolyte Solution
52
Citations
22
References
2002
Year
Bioorganic ChemistryEngineeringOrganic ChemistryChemistryChemical BiologyChemical EngineeringOrganic ElectrochemistryIminium Cation IntermediatesProline DerivativesBiochemistryAnodic OxidationBiomolecular EngineeringElectrochemistryNatural SciencesFundamental ElectrochemistryElectrosynthesisAnodic ModificationDerivative (Chemistry)Synthetic ChemistryAlpha'-phenylsulfanylated N-acylproline Derivatives
[reaction: see text] N-Acyliminium cation of prolines was efficiently generated to accumulate in an undivided cell at 0 degrees C by an anodic oxidation of N-acylprolines or alpha'-phenylsulfanylated N-acylproline derivatives in a lithium perchlorate/nitromethane solution. The iminium cation intermediates gave modified prolines by a reaction with nucleophiles under mild conditions.
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