β-Silicon effect enables direct HAT for enantioconvergent couplings of α-silyl alcohols
Peer-Reviewed Publication
Updates every hour. Last Updated: 3-Nov-2026 03:16 ET (3-Nov-2026 08:16 GMT/UTC)
The high O–H bond strength of common alcohols prevents their direct hydrogen atom transfer (HAT) activation. By leveraging the β-silicon effect in α-silyl alcohols, the research group of Professor Xiao Shen at Wuhan University weaken the O–H bond to enable redox-neutral, photoinduced homolysis using thioxanthone. The resulting alkoxy radicals undergo Brook rearrangement to carbon radicals, which are intercepted by nickel catalysis for enantioconvergent cross-couplings with acyl chlorides and aryl bromides. This protocol tolerates substrates inert under classical SET/PCET conditions and establishes direct HAT as a versatile platform.
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