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) …

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 experimental rate law for the Cu (I)-catalyzed azide− alkyne cycloaddition (CuAAC)
reaction was found to vary in complex ways with concentration, the presence of chloride ion …

The copper-catalyzed azide-alkyne cycloaddition reaction [1](CuAAC)(Scheme 1, a) is
known for its high fidelity in the presence of many functional groups and under demanding …

The 1, 3-dipolar cycloaddition of azides and alkynes [1] is an effective way to make
connections between structures that bear a wide variety of functional groups.[2] The process …

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 copper (I)‐catalyzed azide–alkyne cycloaddition (CuAAC) reaction regiospecifically
produces 1, 4‐disubstituted‐1, 2, 3‐triazole molecules. This heterocycle formation chemistry …

We described in a previous communication a variant of the popular CuI-catalyzed azide−
alkyne cycloaddition (AAC) process where 5 mol% of Cu (OAc) 2 in the absence of any …

The reactions of organic azides and alkynes catalysed by copper species represent the
prototypical examples of click chemistry. The so-called CuAAC reaction (copper-catalysed …

Tris (2-benzimidazolylmethyl) amines have been found to be superior accelerating ligands
for the copper (I)-catalyzed azide− alkyne cycloaddition reaction. Candidates bearing …