The copper-catalyzed cycloaddition reaction between azides and alkynes functions
efficiently in aqueous solution in the presence of a tris (triazolyl) amine ligand. The process …

The copper‐catalyzed azide‐alkyne cycloaddition reaction is widely used for the connection
of molecular entities of all sizes. A protocol is provided here for the process with …

Since its discovery in 2002, the copper-catalyzed azide-alkyne cycloaddition (CuAAC)[1]
reaction—the most widely recognized example of click chemistry [2]—has been rapidly …

The copper-catalyzed azide− alkyne cycloaddition (CuAAC) reaction, optimized for
biological molecules in aqueous buffers, has been shown to rapidly label mammalian cells …

The copper (I)‐catalyzed azide–alkyne cycloaddition (CuAAC) reaction has found broad
application in myriad fields. For the most demanding applications that require high yields at …

The development of selective and site-specific bio-orthogonal conjugation methods is an
important topic in chemical biology. A wide range of methods, such as the Staudinger …

Copper-catalyzed azide–alkyne cycloaddition (CuAAC) has found numerous applications in
a variety of fields. We report here only modest differences in the reactivity of various classes …

The concept of chelation‐assisted copper catalysis was employed for the development of
new azides that display unprecedented reactivity in the copper (I)‐catalyzed azide–alkyne …

The copper (I)‐catalyzed azide–alkyne cycloaddition (CuAAC), the prototypical reaction of
click chemistry, is accelerated by tris (triazolylmethyl) amine‐based ligands. Herein, we …

The copper (I)-catalyzed alkyne azide 1, 3-dipolar cycloaddition (CuAAC) or 'click'reaction, is
a highly versatile reaction that can be performed under a variety of reaction conditions …