A visible-light-induced radical tandem cyclization/arylation between 2-amino-1, 4-
naphthoquinone and N-allyl-2-bromo-2, 2-difluoroacetamides has been developed without …

Metal‐catalysed C− H functionalization has emerged as a powerful platform for the
derivatization of quinones, a class of compounds with wide‐ranging applications. This …

An efficient Rh (III)-catalyzed C–H alkenylation/directing group migration cascade between
indoles and alkynes for the assembly of tetrasubstituted alkenes is reported. The carbamoyl …

Ruthenium-catalysis enabled the C-5 selective C–H oxygenation of naphthoquinones, and
also sets the stage for the site-selective introduction of a hydroxyl group into …

Compounds featuring weakly-coordinating N-oxides or carbonyl groups, as for instance,
quinoline N-oxide and quinonoid systems represent important structural scaffolds with …

Electrochemical selenation in undivided electrochemical cells allows the preparation of
selenium‐containing naphthoquinones. The rapid, green and efficient protocol avoids …

We report a Rh-catalyzed method for the C-5 selective C–H iodination of naphthoquinones
and show that complementary C-2 selective processes can be achieved under related …

We report a sequential C–H iodination/organoyl-thiolation of naphthoquinones and their
relevant trypanocidal activity. Under a combination of AgSR with a copper source, sulfur …

Rhodium (III) catalyzed regioselective C–H alkylation and alkenylation at the C5 position of
1, 4-naphthoquinone with maleimides under acidic and basic conditions, respectively, is …

Herein, we describe the Ru‐catalyzed C− H alkenylation of 1, 4‐naphthoquinones (1, 4‐
NQs), resulting in 1, 4‐naphthoquinoidal/SuFEx hybrids with moderate to good yields. This …