The enantioselective oxidative C-H functionalization of tetrahydroisoquinoline derivatives is achieved through

The enantioselective oxidative C-H functionalization of tetrahydroisoquinoline derivatives is achieved through the merger of photoredox and asymmetric anion-binding catalysis. parlayed towards the useful era of synthetically useful high-energy organic intermediates such as for example free of charge radicals2 and radical anions and cations.3 4 Successful initiatives to induce enantioselective catalytic control in such photocatalyzed functions… Continue reading The enantioselective oxidative C-H functionalization of tetrahydroisoquinoline derivatives is achieved through