The reductive activation of C-N bonds via single-electron transfer enables the generation of radicals from readily available and abundant amines. Despite their potential, such transformations remain challenging because of the stability of the C-N bond and its pre-activation is therefore often required to facilitate its cleavage. In this context, quaternary ammonium salts constitute ideal amine-derived radical precursors as they are stable and easy to handle, in addition to enabling the design of atom economical processes. In this Synpact article, we highlight our recent work describing the photoredox-catalyzed reductive activation of ammonium salts. Several ammonium salts could indeed be successfully activated using iridium photoredox catalysis, the corresponding radicals being subsequently engaged in hydrodeamination reactions and radical couplings. Moreover, the reactivity observed experimentally could be correlated to the ammonium salts’ redox potentials that were determined using cyclic voltammetry.
1 Introduction
2 Hydrodeamination of benzylic and aryl ammonium salts
3 Selective activation and extension to radical couplings
4 Determination of the redox potentials of ammonium salts
5 Conclusion
