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 …

During the past years, a variety of scientific and methodological developments have been
achieved, which urge chemists to increase the tools of their arsenal to improve the ease and …

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) …

The modification of polymers after the successful achievement of a polymerization process
represents an important task in macromolecular science. Cycloaddition reactions, among …

CuI‐catalyzed alkyne–azide cycloaddition provides 1, 4‐disubstituted 1, 2, 3‐triazoles with
such efficiency and scope that the transformation has been described as “click” chemistry …

The concept of “click” chemistry, introduced by Sharpless and coworkers a couple of years
ago, promotes the use of efficient, selective and versatile chemical reactions in synthetic …

An efficient and improved procedure for the preparation of aromatic azides and their
application in the Cu (I)-catalyzed azide− alkyne 1, 3-dipolar cycloaddition (“click reaction”) …

2.1. 1. The Copper Catalyst 2.1. 2. Auxiliary Ligands 2.2 Studies of the Mechanism of
CuAAC 2.3. The Cyclodimerization Phenomenon 2.4. One-Pot CuAAC Procedure 2.5 …

The development of selective chemistries that are orthogonal to the diverse array of
functional groups present in many polymeric systems is becoming an important tool for the …