Electrochemistry, which employs electrons as reagents and avoids the use of traditional
redox reagents, becomes a powerful tool in oxidative dehydrogenation cross-coupling …

The development of novel synthetic strategies to form new chemical entities in a
stereoselective manner is an ongoing significant objective in organic and medicinal …

Asymmetric catalytic multicomponent cascade reactions have become indispensable tools
for enantioselective construction of spirooxindoles. In recent years, a number of successful …

Research and industrial interest in radical C–H activation/radical cross-coupling chemistry
has continuously grown over the past few decades. These reactions offer fascinating and …

In recent years, transition‐metal‐catalyzed C− H activation has become a key strategy in the
field of organic synthesis. Rhodium complexes are widely used as catalysts in a variety of …

Chiral spirooxindoles are privileged heterocyclic motifs, which are widely found in natural
alkaloids and pharmaceuticals. Moreover, the construction of chiral spiro-cyclic frameworks …

Conspectus 3, 3-Disubstituted oxindoles are widely distributed in natural products, drugs,
and pharmaceutically active compounds. The absolute configuration and the substituents on …

The indole scaffold will continue to play a vital part in the future of drug discovery and
agrochemical development. Because of this, the necessity for elegant techniques to enable …

In contrast to Lewis-acid catalysts, Brønsted acids have been employed primarily as
catalysts for the formation and cleavage of C− O bonds, such as hydrolysis and formation of …

Silver nanoparticles-decorated Preyssler functionalized cellulose biocomposite (PC/AgNPs)
was prepared and fully characterized by FTIR, UV–vis, SEM, and TEM techniques. The …