Transition‐metal‐catalyzed site selective arene C− H bond activation concomitant
functionalization with various coupling partners gain magnificent attraction in synthetic …

The last two decades or so have witnessed an upsurge in defining the art of designing
complex natural products and nature-inspired molecules. Throughout these decades …

As a powerful synthon, pyrazolone has widely been exploited for the construction of various
chiral pyrazoles/pyrazolones which hold great potential in the development of …

Herein, we report the additive-controlled divergent synthesis of tetrasubstituted 1, 3-enynes
and alkynylated 3 H-pyrrolo [1, 2-a] indol-3-ones through rhodium-catalyzed C–H …

By virtue of a synergistically dual-directing-group (the O–NHAc part and the hydroxyl group)-
assisted strategy, the efficient and practical Rh (III)-catalyzed regioselective redox-neutral C …

The development of transition‐metal catalyzed enantioselective and diastereoselective
transformations has contributed many advances in the field of synthetic organic chemistry …

A simple and efficient Se-radical triggered cyclization/substitution cascade reaction of alkyne-
tethered cyclohexadienones to afford 5-hydroxy-3-selenyl-4a, 8a-dihydro-2H-chromen-6 …

A facile and efficient approach for the direct thiocyanation of pyrazolin-5-ones via a radical
mechanism has been established for the first time. A series of 4-thiocyanated 5-hydroxy-1H …

A rhodium-catalyzed diastereoselective formal [5+ 2] annulation of indoles with
cyclohexadienone-containing 1, 6-enynes has been established via indole 2, 3 …

Manganese (I)-catalyzed C–H activation of indoles and divergent annulative coupling with
alkyne-tethered cyclohexadienones has been realized under operationally simple …