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<i>N</i>-Heterocyclic Carbene Organocatalytic Reductive β,β-Coupling Reactions of Nitroalkenes via Radical Intermediates
91
Citations
47
References
2014
Year
EngineeringOrganic ChemistryChemistryNhc OrganocatalysisNovel Organocatalystsβ-Carbon CouplingOrganometallic CatalysisRedox Chemistryβ-Coupling ReactionsCross-coupling ReactionBiochemistryRadical IntermediatesCatalysisCatalytic SynthesisBiomolecular EngineeringCatalytic Redox ProcessHeterocyclicNatural SciencesMolecular Catalysis
An unprecedented N-heterocyclic carbene catalytic reductive β,β-carbon coupling of α,β-nitroalkenes, by using an organic substrate to mimic the one-electron oxidation role of the pyruvate ferredoxin oxidoreductase (PFOR) in living systems, has been developed. The reaction goes through a radical anion intermediate generated under a catalytic redox process. For the first time, the presence of radical anion intermediate in NHC organocatalysis is observed and clearly verified.
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