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 …

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 …

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 unsupported nanoporous gold catalyst was firstly been reported for catalyzing the highly
selective semihydrogenation of alkynes with organosilanes and water as the hydrogen …

Within the green chemistry context, heterogeneous catalysis applied to organic synthesis is
becoming an increasingly important field, bringing its own innovation and specific properties …

Self-assembly of copper sulfate and a poly (imidazole–acrylamide) amphiphile provided a
highly active, reusable, globular, solid-phase catalyst for click chemistry. The self-assembled …

A one-pot procedure for the synthesis of 1, 2, 3-triazole derivatives by a three-component
coupling of alkyl (benzyl) halides or aryl boronic acids, sodium azide and terminal alkynes …

The cyclization reactions of alkynes have become one of the most important and useful
methodologies for the preparation of heterocycles. To this end, the association between …

We report for the first time the highly efficient and regioselective hydrogenation of quinoline
derivatives to 1, 2, 3, 4-tetrahydroquinolines using unsupported nanoporous gold as the …

With increasing advances on nanotechnology, the nanostructured copper catalysts have
attracted much attention in alkyne–azide click reaction in the last few years owing to their …