The cathodic cleavage of aromatic sulphonamides: an elegant way to produce amino radicals themselves fully characterized by means of the spin marking technique

Sulphonamides may lead, in the course of their cathodic cleavage, to intermediate amino radicals. These radicals may be reduced or trapped rapidly by nitrones added “ in situ ”. The method allows (by means of ESR spectral analysis) elements for establishing cleavage mechanisms to be obtained.