A cascade reaction enabling the construction of pyrrolo3,4‐ b indole core from electron‐deficient and benzophenone‐derived isocyanide precursors under phase‐transfer conditions is described. This transformation proceeds in the presence of a quaternary ammonium catalyst and cesium carbonate, affording functionalized polycyclic cores. The reaction follows the interrupted Barton–Zard reaction pathway and tolerates a broad range of 3‐nitroindole and isocyanide substrates. Performed control experiments provide insight into the generally moderate product yields and clarify why the reaction is not amenable to asymmetric induction.
Mikleušević et al. (2026) studied this question.