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 …

The applications of copper (Cu) and Cu-based nanoparticles, which are based on the earth-
abundant and inexpensive copper metal, have generated a great deal of interest in recent …

The allotropes of carbon nanomaterials (carbon nanotubes, graphene) are the most unique
and promising substances of the last decade. Due to their nanoscale diameter and high …

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 …

The copper‐catalyzed azide/alkyne cycloaddition reaction (CuAAC) has emerged as the
most useful “click” chemistry. Polymer science has profited enormously from CuAAC by its …

This review is focused on the mechanistic aspects and recent trends of the metal-catalyzed
azide-alkyne cycloaddition (MAAC) so-called “click” reactions with catalysts based on …

Over the course of the past 15 years the success story of N-heterocyclic carbene (NHC)
compounds in organic, inorganic, and organometallic chemistry has been extended to …

Conspectus Click chemistry has emerged as a significant tool for materials science, organic
chemistry, and bioscience. Based on the initial concept of Barry Sharpless in 2001, the …

The world is rapidly changing, the resources are getting depleted, and the demand for
newer technologies and products is increasing. To keep up with these new advances, highly …

The copper (I)-catalyzed azide− alkyne cycloaddition (CuAAC) reaction is considered to be
the most representative ligation process within the context of the “click chemistry” concept …