Arylative Cyclization of 2‑Isocyanobiphenyls with Anilines: One-Pot Synthesis of 6‑Arylphenanthridines via Competitive Reaction Pathways

Abstract

A transition-metal-free method for the synthesis of C6 phenanthridine derivatives by arylative cyclization of 2-isocyanobiphenyls with arylamines in one pot was developed. Mechanistic studies suggest that electrophilic aromatic substitution (S<sub>E</sub>Ar) of a nitrilium intermediate and homolytic aromatic substitution (HAS) of an imidoyl radical intermediate are two competitive reaction pathways involved in the annulation step

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