Multicomponent reactions are operationally simple and display a significant role in diverse
chemical modification by reducing reaction times as well as additional steps involved. In this …

The current study delves into the mechanistic intricacies of azide-alkyne cycloaddition
reactions (MAAC) catalyzed by transition metals (M= Cu, Ag, and Au) bound to N …

This study investigated the catalytic behavior of NHC-X ligands (X= F, Cl, Br, I) in
cycloaddition reactions, focusing on both mononuclear and binuclear pathways. Using NCI …

This study evaluated the catalytic efficiency of Au (I), Ag (I), and Cu (I) complexes in the
azide‒alkyne cycloaddition (AAC) reaction through density functional theory (DFT) …

Chiral recognition is one of the most important and fascinating areas in supramolecular
chemistry. Chiral macrocycles, especially chiral macrocyclic hosts, having stable structures …

Click chemistry and bioorthogonal chemistry have significantly advanced the field of
chemical biology by enabling the precise and selective modification of biomolecules in …

Intramolecular click chemistry has become a valuable technique in the synthesis of complex
molecular architectures due to its high efficiency, selectivity, and ability to proceed under …

The Cu (I)-catalyzed azide-alkyne cycloaddition (CuAAC), a model click chemistry reaction
pivotal in synthesizing diverse 1, 4-disubstituted 1, 2, 3-triazoles with great ease. This …

Some new (S)-2-[1-aryl-5-methyl-1 H-1, 2, 3-triazol-4-yl]-4-benzyl-4, 5-dihydro-oxazoline
were synthesized by the reaction of (S)-N-(1-hydroxy-3-phenylpropan-2-yl)-1-aryl-5-methyl …

The term “Click Chemistry”, first coined by KB Sharpless of the Scripps Research Institute in
2001, addresses a particular type of reactions that afford products in high yields with …