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PCET-mediated deconstructive cross-coupling of aliphatic alcohols

A practical deconstructive arylation of aliphatic alcohols has been developed using a synergistic photoredox proton-coupled electron transfer (PCET) and nickel dual catalytic system. The method efficiently generates alkyl radicals via… Click to show full abstract

A practical deconstructive arylation of aliphatic alcohols has been developed using a synergistic photoredox proton-coupled electron transfer (PCET) and nickel dual catalytic system. The method efficiently generates alkyl radicals via concerted PCET-mediated β-scission, enabling the formation of C(sp3)–C(sp2) bonds between alcohols and aryl halides. Optimization studies revealed a broad functional group tolerance and high chemoselectivity, with good yields even for challenging tertiary alcohol substrates. Mechanistic insights from transient absorption spectroscopy confirmed the dominance of a PCET pathway for radical generation. This strategy expands the utility of alcohols as alkyl radical precursors in cross-coupling reactions, offering a versatile tool for constructing complex molecular architectures.

Keywords: mediated deconstructive; deconstructive cross; cross coupling; aliphatic alcohols; pcet mediated

Journal Title: Chemical Science
Year Published: 2025

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