Complementary pathways in C–H functionalization of furfural derivatives with cobalt-hydride catalysis
Abstract
This study reports the first cobalt-catalysed C–H functionalization of furfural derivatives, demonstrating distinct reactivities based on the substrate. Furfurylimines enable selective C5–H alkenylation with alkynes, whereas free aldehydes undergo decarbonylative C2-alkenylation. These results establish a novel strategy using formyl groups as traceless handles for cobalt-catalysed C–C bond formation.
- This article is part of the themed collection: The Functionalization of Unreactive Carbon-Hydrogen Bonds