Catalyst-free photoinduced selective oxidative C(sp3)-C(sp3) bond cleavage in arylamines

Due to the directional nature of sp(3)-hybridized orbitals and the absence of pi-orbitals, the oxidative cleavage of the kinetically and thermodynamically stable C(sp(3))-C(sp(3)) bond is extremely difficult and remains scarcely explored. In this work, under the double argument of quantum mechanics (QM) computations and meticulous experiments on our well-designed C-C single bond cleavage mechanism, we discovered a means of photoinduced selective oxidative C(sp(3))-C(sp(3)) bond cleavage in arylamines, easily achieved by simple visible light irradiation using O-2 as a benign oxidant under very mild conditions. The utility of our methodology was demonstrated by the C(sp(3))-C(sp(3)) bond cleavage in morpholine/piperazine arylamines with excellent functional group tolerance. Importantly, our methodology is noteworthy, not only in that it does not require any catalysts, but also in that it provides valuable possibilities for the scalable functionalization of clinical drugs and natural products.

Automated summary

The study discovered a new photoinduced selective oxidative method to cleave C(sp(3))-C(sp(3) bonds under mild conditions, with excellent functional group tolerance, by utilizing quantum mechanics computations and meticulous experiments. This catalyst-free approach offers valuable possibilities for the scalable functionalization of clinical drugs and natural products.