Unusual Transformation of the 3-Hydroxy-picolinoyl Residue of Pristinamycin IA

Pristinamycin IA was modified in a two-step procedure to give original derivatives possessing a tricyclic nucleus (8a, 8b, 8c) or a substituted pyrrole ring (10a, 10b) in place of the natural exocyclic 3-hydroxy-picolinoyl residue. This transformation involved firstly preparation of pyridinium betaines 5 from pristinamycin IA and secondly a 1-3 dipolar cycloaddition between 5 and N-substituted maleimides or diethyl ace tylenedicar boxy late. The compounds obtained were evaluated as antibacterial agents alone and in association with pristinamycin IIA.