C–H activation has surfaced as an increasingly powerful tool for molecular sciences, with
notable applications to material sciences, crop protection, drug discovery, and …

C–H bond activation and decarboxylation are two significant processes in organic synthesis.
The combination of these processes provides a novel synthetic strategy, that is …

Catalytic cross-coupling reactions of aromatic esters and amides have recently gained
considerable attention from synthetic chemists as de novo and efficient synthetic methods to …

Over the last decade, substantial research has led to the introduction of an impressive
number of efficient procedures which allow the selective construction of C C bonds by …

Transition-metal-catalyzed decarbonylation via carbon–carbon bond cleavage is an
essential synthetic methodology. Given the ubiquity of carbonyl compounds, the selective …

C− C bond forming reactions incarnate the core of organic synthesis because of their
fundamental applications to molecular diversity and complexity. In recent years, use of …

The direct decarboxylative arylation of α-amino acids has been achieved via visible light-
mediated photoredox catalysis. This method offers rapid entry to prevalent benzylic amine …

While the synthesis of biaryls has advanced rapidly in the past decades, cross-Ullman
couplings of aryl chlorides, the most abundant aryl electrophiles, have remained elusive …

Abstract The first Ni‐catalyzed Suzuki–Miyaura coupling of amides for the synthesis of
widely occurring biaryl compounds through N− C amide bond activation is reported. The …

Sulfur utilization is a global concern because of its abundant nature sources and the safety
or environmental problems caused by its burning or oxidation during storage, while sulfur …