A catalytic N-deacylative alkylation approach to hexahydropyrrolo[2,3-b]indole alkaloids

Abstract

A versatile unprecedented strategy to diversely functionalized hexahydropyrrolo[2,3-b]indole alkaloids is described in high chemical yields. The synthesis features a key Pd(0)-catalyzed deacylative alkylation of N-acyl 3-substituted indoles using only 1 mol% of Pd(PPh₃)₄. The scope of this methodology is further defined in the asymmetric synthesis of pyrroloindolines using a diastereoselective approach.