Abstract
Common cross-coupling reactions to obtain C(sp<sup>2</sup>)–C(sp<sup>3</sup>)-bonds are hampered by the abundance of nucleophilic and electrophilic functional groups. Recently in <i>Nature</i>, Dong and MacMillan developed a mild activation of a diverse range of alcohols with an <i>N</i>-heterocyclic carbene (NHC) salt and merged it with nickel photoredox dual catalytic arylation.
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