Rh(III)-Catalyzed Synthesis of Substituted Isoindoles through a Direct C–H Activation/[4 + 1] Annulation and Acyl Migration Cascade of Oxadiazolones with Diazo Compounds

Abstract

A Rh(III)-catalyzed C-H bond activation for the synthesis of fused 2<i>H</i>-isoindole scaffolds from oxadiazolones with diazo compounds was developed. The reaction proceeded through C-H activation of oxadiazolones/[4 + 1] annulation, intramolecular cyclization, and an unusual acyl migration cascade to afford target scaffolds with good yields. These 2<i>H</i>-isoindole derivatives could be further transformed into intriguing drug privileged scaffolds.