An efficient stereoselective route for the synthesis of cyclopentene fused 2-pyrrolines has
been established via a Pd-catalyzed C–H activation/oxidative coupling of aryl enamides with …

A novel and efficient palladium (II)-catalyzed alkenyl C–H activation oxidative annulation of
enamides with alkynes for the synthesis of substituted pyrroles has been developed. The …

Ruthenium-Catalyzed Pyrrole Synthesis via Oxidative Annulation of Enamides and Alkynes |
Organic Letters ACS ACS Publications C&EN CAS Find my institution Log In Organic Letters …

Palladium-catalyzed dearomative [2+ 2+ 1] annulations of aryl ethers with alkynes are
reported via para-selective C–H functionalization, providing highly functionalized …

A novel palladium-catalyzed oxidative cyclopropanation of enamides and norbornenes has
been developed. The reaction proceeded through palladium-catalyzed vinyl C–H bond …

Direct C (3) alkenylation of non-aromatic enamides through palladium (II)-catalyzed
Fujiwara–Moritani cross-coupling was developed. The reaction scope includes a range of …

A method for intramolecular sp2 C–H oxidative arylation of unactivated cyclic olefins has
been developed to access spiro-dihydroquinoline and octahydrophenanthrene derivatives …

A new, metal-free I2-catalyzed oxidative tandem annulation of 1, 6-enynes by employing tert-
butyl hydroperoxide (TBHP) as the oxidant and the oxygen atom resource for the synthesis …

An efficient Pd (II)-catalyzed oxidative annulation of 2-hydroxynaphthalene-1, 4-diones and
internal alkynes has been developed with high step efficiency. A broad range of functional …

Palladium‐Catalyzed Oxidative Annulation via CH/NH Functionalization: Access to
Substituted Pyrroles - Peng - 2013 - Advanced Synthesis & Catalysis - Wiley Online Library Skip …