Efficient methods have been developed to synthesize azetidine, pyrrolidine, and indoline
compounds via palladium-catalyzed intramolecular amination of C–H bonds at the γ and δ …

Within this review, recent developments in the field of C (sp 3)–H activation catalyzed by
palladium are discussed. Both intra-and intermolecular reactions towards carbon–carbon …

Palladium‐catalyzed C–H activation/C–C bond‐forming reactions have emerged as a
promising class of synthetic tools in organic chemistry. Among the many different means of …

We report an efficient method for the alkylation of γ-C (sp3)–H bonds of picolinamide-
protected aliphatic amine substrates with primary alkyl iodides via palladium catalysis …

Abstract PdII‐catalyzed C (sp3)− H olefination of weakly coordinating native amides is
reported. Three major drawbacks of previous C (sp3)− H olefination protocols, 1) in situ …

Conspectus Aromatic structures are widespread motifs throughout organic chemistry, and C–
H activation has been recognized as a major tool for enabling their sustainable and efficient …

Direct selective palladium catalyzed C–H functionalization has become a highly attractive
strategy in organic synthesis and represents a highly desirable goal. Compared with cross …

The development of readily tunable and regioselective C–H functionalization reactions that
operate solely through catalyst control remains a challenge in modern organic synthesis …

A new palladium-catalyzed C (sp3)–H amination reaction has been developed. 1-(tert-Butyl)-
2-iodobenzene and its derivatives undergo palladium-catalyzed C–H activation to form …

This report describes a carboxylate ligand exchange strategy that was used to achieve a
Catellani reaction consisting of amination/unactivated aliphatic C–H arylation. Pivalic acid …