The present review is devoted to the application of transition metal complexes with such
ligands as amino acids, peptides and carbohydrates in catalysis. The literature published …

Immediately after the invention of 'Click Chemistry'in 2002, the regioselective 1, 2, 3-triazole
scaffolds resulted from respective organic azides and terminal alkynes under Cu (I) catalysis …

This report describes a convenient method for the Cu (I)-catalyzed Sonogashira cross-
coupling reaction of aryl/heteroaryl halides and alkynyl sugars in the presence of a 1, 2, 3 …

Abstract A novel organocatalyzed [3+ 2] cycloaddition reaction of nitroolefins with glycosyl
azides as well as organic azides has been developed for successful construction of 1, 5 …

Click Chemistry, a modular, rapid, and one of the most reliable tool for the regioselective 1,
2, 3‐triazole forming [3+ 2] reaction of organic azide and terimal alkyne is widely explored in …

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 …

We herein report a multicomponent reaction for the synthesis of N-unsubstituted-1, 2, 3-
triazoles and N-substituted-1, 2, 3 triazoles from the reaction of aldehydes, nitroalkanes, and …

This report describes a convenient method for the Cu (I)-catalyzed tandem synthesis of
dihydrophenanthridinediones and substituted isoquinolinones with the assistance of …

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

Soon after that invention of modular 'CuAAC Click Chemistry'by two independent group of
researchers, Morten Meldal and Karl Barry Sharpless in 2002, Carolyn Bertozzi introduced …