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The N-heterocyclic carbene (NHC)-catalysed redox amidation reaction is poorly developed and usually requires catalytic co-additives for electron-rich amine nucleophiles. We report a masking strategy (using CO2) that couples release of the free amine nucleophile to catalytic turnover, and in doing so, enables direct catalytic redox amidation of electron-rich amines.

Direct NHC-catalysed redox amidation using CO2 for traceless masking of amine nucleophiles

Direct NHC-catalysed redox amidation using CO₂ for traceless masking of amine nucleophiles