Direct N-allylation of azoles with hydrogen
evolution
has been achieved through the synergistic combination of organic photocatalysis
and cobalt catalysis. The protocol bypasses stoichiometric oxidants
and prefunctionalization of alkenes and produces hydrogen (H2) as the byproduct. This transformation highlights high step- and
atom-economy, high efficiency, and broad functional group tolerance
for further derivatization, which opens a door for C–N bond
formation that is valuable in heterocyclic chemistry