A method for remote radical C-H alkynylation and amination of diverse aliphatic alcohols has been developed. The reaction features a copper nucleophile complex formed as a photocatalyst, which reduces the silicon-tethered aliphatic iodide to an alkyl radical to initiate 1,-hydrogen atom transfer. Unactivated secondary and tertiary C-H bonds at β, γ, and δ positions can be functionalized in a predictable manner.
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| http://dx.doi.org/10.1039/d0sc05883a | DOI Listing |
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