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 …

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 …

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 …

A versatile and highly efficient catalyst for the Huisgen cycloaddition reaction has been
developed. Previously isolated or in situ generated azides yielded 1, 2, 3‐triazoles with …

Click chemistry, designated by Sharpless and his coworkers, is a modular approach that
uses only the most practical and reliable chemical transformations. The Huisgen reaction …

The “click” concept, proposed by Sharpless, Kolb, and Finn in 2001, is undeniably one of the
most noticeable synthetic trends in this new century.[1] The catchy term “click” refers to …

A one-pot reaction for Cu (II)-catalyzed diazo transfer and Cu (I)-catalyzed azide− alkyne 1,
3-dipolar cycloaddition (sometimes called click reaction) is reported. 1, 4-Disubstituted 1, 2 …

The Cu (I)-catalyzed azide-alkyne cycloaddition reaction, also known as click chemistry, has
become a useful tool for the facile formation of 1, 2, 3-triazoles. Specifically, the utility of this …

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 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 …