Expanding the chemical space of enol silyl ethers: catalytic dicarbofunctionalization enabled by iron catalysis

Enol silyl ethers are versatile, robust, and readily accessible substrates widely used in chemical synthesis. However, the conventional reactivity of these motifs has been limited to classical two electron (2-e) enolate-type chemistry with electrophilic partners or as radical acceptors in one electron (1-e) reactivity leading, in both cases, to exclusive alpha-monofunctionalization of carbonyls. Herein we describe a mild, fast, and operationally simple one-step protocol that combines readily available fluoroalkyl halides, silyl enol ethers, and, for the first time, hetero(aryl) Grignard reagents to promote selective dicarbofunctionalization of enol silyl ethers. From a broader perspective, this work expands the synthetic utility of enol silyl ethers and establishes bisphosphine-iron catalysis as enabling technology capable of orchestrating selective C-C bond formations with short-lived alpha-silyloxy radicals with practical implications towards sustainable chemical synthesis. Herein, we report the dicarbofunctionalization of enol silyl ethers via an Fe-catalyzed decoupled cross-coupling of (fluoro)alkyl halides, and enol silyl ethers.