Alkenes and their derivatives are featured widely in a variety of natural products,
pharmaceuticals, and advanced materials. Significant efforts have been made toward the …

C− H activation reactions with high catalyst turnover numbers are still very rare in the
literature and 10 mol% is a common catalyst loading in this field. We offer a representative …

Transition-metal-catalyzed C–H bond functionalizations have had an enormous influence on
organic synthesis in recent times. However, the use of low-abundance 4d and 5d metals is …

Cp* Cobalt (III)-catalyzed enantioselective C–H amidation of ferrocenes using
monoprotected amino acids (MPAAs) as chiral ligands was developed. The reaction was …

A Lewis base catalyst Trip-SMe (Trip= triptycenyl) for electrophilic aromatic halogenation
using N-halosuccinimides (NXS) is introduced. In the presence of an appropriate activator …

During the last two decades, impressive advancements have been achieved in transition
metal‐catalyzed chelation‐assisted C—H functionalization reaction. While reactions in this …

The ubiquity of carbon halogen bonds in the structural core of numerous biomolecules and
pharmaceuticals along with their role as synthetic precursors in various organic reactions …

A novel Pd-catalyzed enantioselective aminochlorination of alkenes via a 6-endo cyclization
is reported herein, which provides easy access to a wide array of structurally diverse 3 …

The palladium-catalyzed C–H iodination of 1-arylpyridine N-oxides proceeded under
electrochemical oxidation conditions using I2 as an iodine source. The reaction of …

A simple and practical synthetic approach for synthesis of aromatic halides is developed.
Simple Lewis base, DABCO, is used as the catalyst. This arene halogenation process …