Parallel paired electrolysis-enabled asymmetric catalysis: simultaneous synthesis of aldehydes/aryl bromides and chiral alcohols

Metal-catalyzed asymmetric electro-reductive couplings have emerged as a powerful tool for organic synthesis, wherein a sacrificial anode is typically required. Herein, a parallel paired electrolysis (PPE)-enabled asymmetric catalysis has been developed, and the alcohols and ketones could be simultaneously converted to the corresponding aldehydes and chiral tertiary alcohols with high yields and enantioselectivity in an undivided cell. Additionally, this Ni-catalyzed asymmetric reductive coupling can well match the anodic oxidative C–H bond bromination of (hetero)arenes. This protocol opens an alternative avenue for organic synthesis.