Catalytic Kinetic Resolution by Enantioselective Aromatization: Conversion of Racemic Intermediates of the Barton–Zard Reaction into Enantioenriched 3‐Arylpyrroles

Racemic 3,4‐dihydro‐2 H ‐pyrroles, hypothetical intermediates of the Barton–Zard reaction, were synthesized in a highly diastereoselective manner and fully characterized for the first time. Kinetic resolution of the dihydropyrroles with a quinine‐derived thiourea afforded the (+)‐3‐arylpyrrole products and recovered (+)‐3,4‐dihydro‐2 H ‐pyrroles with high efficiency (s‐factor up to 153). The resolved (+)‐3,4‐dihydro‐2 H ‐pyrroles underwent subsequent aromatization with a quinidine‐derived thiourea catalyst to afford (−)‐3‐arylpyrroles with excellent central‐to‐axial chirality transfer. In contrast to the well‐accepted Barton–Zard mechanism, the aromatization of the 3,4‐dihydro‐2 H ‐pyrroles in the presence of a bifunctional catalyst is believed to proceed by an unprecedented sequence involving syn  elimination of HNO 2 and aromatization.