Bi-Catalyzed 1,2-Reactivity of Spirocyclopropyl Oxindoles with Dithianediol: Access to Spiroheterocycles.

Abstract

The efficient Bi-catalyzed 1,2-reactivity of spirocyclopropyl oxindoles has been disclosed with dithianediols as the sulfur surrogate to furnish spiroheterocycles at moderate temperature. The procedure provides a potential approach for the construction of spirotetrahydrothiophene scaffolds with functional group diversity. The catalytic 1,2-reactivity of cyclopropanes, mechanistic studies using density functional theory studies, diastereoselectivity, and additive-free mild conditions are the important practical features.