Cobalt-Hydride-Catalyzed Alkene-Carboxylate Transposition (ACT) of Allyl Carboxylates

Abstract

The alkene-carboxylate transposition (ACT) of allyl carboxylates is one of the most atom-economic and synthetically reliable transformations in organic chemistry, as allyl carboxylates are versatile synthetic intermediates. Classic ACT transformations, including [3,3]-sigmatropic rearrangement and transition metal-catalyzed allylic rearrangement, typically yield 1,2-alkene/1,3-acyloxy shifted products through a two-electron process. However, position-altered ACT to produce distinct 1,3-alkene/1,2-acyloxy shifted products remains elusive. Here, we report the first cobalt-hydride-catalyzed ACT of allyl carboxylates, enabling access to these unprecedented 1,3-alkene/1,2-acyloxy shifted products via a 1,2-radical migration (RaM) strategy. This transformation demonstrates broad functional group tolerance, is suitable for late-stage modification of complex molecules, and is amenable to gram-scale synthesis. It also expands the reaction profiles of both allyl carboxylates and cobalt catalysis. Preliminary experimental and computational studies suggest a mechanism involving metal-hydride hydrogen atom transfer (MHAT) and the 1,2-RaM process. This reaction is expected to serve as the basis for the development of versatile Co–H-catalyzed transformations of allyl carboxylates, generating a wide array of valuable building blocks for synthetic, medicinal, and materials chemistry.