Copper (I)-catalyzed 1, 3-dipolar cycloaddition between organic azides and terminal
alkynes, commonly known as CuAAC or click chemistry, has been identified as one of the …

Cu (I)-catalyzed azide–alkyne 1, 3-dipolar cycloaddition (CuAAC), popularly known as the
“click reaction”, serves as the most potent and highly dependable tool for facile construction …

A short overview of the copper (I)-catalyzed azide alkyne cycloaddition (CuAAC), the most
used “click” reaction, is presented, including the introduction of the “click” concept, the …

The Huisgen 1, 3-dipolar cycloaddition reaction of organic azides and alkynes1, 2 has
gained considerable attention in recent years due to the introduction in 2001 of Cu (1) …

In recent years, there has been an ever‐increasing need for rapid reactions that meet the
three main criteria of an ideal synthesis: efficiency, versatility, and selectivity. Such reactions …

Dipolar cycloaddition reactions can be considered a powerful synthetic tool in the building of
heterocyclic rings, with applications in different fields. In this review we focus on the …

The metal catalyzed azide/alkyne 'click'reaction (a variation of the Huisgen 1, 3‐dipolar
cycloaddition reaction between terminal acetylenes and azides) has vastly increased in …

The synthesis of novel well-defined alkyne side chain functional polymers featuring narrow
molecular weight distributions (PDI= 1.09− 1.17) by living radical polymerization is …

The CuAAC “click” reaction has developed as one of the most useful and widely employed
reactions in ligation within polymer chemistry. This is due to the unique properties of the Cu …

Macrocyclic compounds are of growing interest because of their natural existence, their
interesting biological, physicochemical properties, and potential applications in medicine. 1 …