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 …

The research on 1, 2, 3-triazoles has been lively and ever-growing since its stimulation by
the advent of click chemistry. The attractiveness of 1H-1, 2, 3-triazoles and their derivatives …

Copper (I)-catalyzed azide-alkyne cycloaddition has become a commonly employed method
for the synthesis of complex molecular architectures under challenging conditions. Despite …

This review covers the advances made in the synthesis of luminescent transition metal
complexes containing N-heterocyclic carbene (NHC) ligands. The presence of a high field …

Gold has emerged as a powerful synthetic tool in the chemist's arsenal. From the early use
of inorganic salts such as AuCl and AuCl3 as catalysts, the field has evolved to explore …

Copper (I)-catalyzed azide–alkyne cycloaddition (CuAAC) is an essential “click chemistry”
reaction that is widely used in chemical biology, medicinal chemistry and materials science …

A significant challenge for scientists today is to design green and eco‐friendly catalysts
based on green chemistry with high catalytic performance and recycling properties. Many …

The copper (I)-catalyzed Huisgen dipolar cycloaddition of terminal alkynes 1 with azides 2
[1] to yield 1, 4-and 1, 4, 5-substituted 1, 2, 3-triazoles 3 (azide–alkyne cycloaddition; AAC …

In the search for fundamentally new, active, stable, and readily synthetically accessible
cycloalkynes as strain-promoted azide–alkyne cycloaddition (SPAAC) reagents for …

The prominent role of gold‐N‐heterocyclic carbene (NHC) complexes in numerous research
areas such as homogeneous (photo) catalysis, medicinal chemistry and materials science …