pharmaceutical chemists. Sustainable photoredox-and electrochemical processes were
employed to facilitate the relatively less explored radical cross-electrophile coupling to
access trifluoromethyl-and allyl-substituted tert-alcohols. Reactions proceed through
trifluoromethyl ketyl radical and allyl radical intermediates, which undergo challenging
radical-radical cross-coupling. The developed transformations are mild and chemo-selective …