Redox-neutral rhodium(iii)-catalyzed chemo- and regiospecific [4+1] annulation between benzamides and alkenes for the synthesis of functionalized isoindolinones

Herein, using electron-deficient alkenes embedded with an oxidizing function/leaving group as a rare and nontraditional C-1 synthon, we have achieved the redox-neutral Rh(iii)-catalyzed chemo- and regioselective [4 + 1] annulation of benzamides for the synthesis of functionalized isoindolinones. This method features broad substrate scope, good to excellent yields, excellent chemo- and regioselectivity, good tolerance of functional groups and mild external-oxidant-free conditions.

Automated summary

In this study, an electron-deficient alkene embedded with an oxidizing function/leaving group was used as a rare and nontraditional C-1 synthon to achieve a redox-neutral Rh(iii)-catalyzed chemo- and regioselective [4 + 1] annulation of benzamides for the synthesis of functionalized isoindolinones. This method demonstrated a broad substrate scope, good to excellent yields, excellent chemo- and regioselectivity, good tolerance of functional groups, and mild external-oxidant-free conditions.