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 …

Advances in the chemical synthesis of C-pyranosides/furanosides are summarized, covering
the literature from 2000 to 2016. The majority of the methods take advantage of the …

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 …

This Review summarizes close to 500 primary publications and surveys published since
2000 about the syntheses and diverse bioactivities of C-glycopyranosyl (het) arenes. A …

Triazoles find applications in several major technological areas, and especially in drug
discovery. The click-chemistry approaches based on Huisgen's cycloaddition reaction are …

The β-enaminone–azide cycloaddition has been used for the synthesis of arylselanyl-1H-1,
2, 3-triazole-4-carboxylates by reaction of azidophenyl arylselenides with β-keto-esters. The …

Mechano‐activated chemistry is a powerful tool for remodeling of synthetic polymeric
materials, however, few reactions are currently available. Here we show that using …

Click reactions between alkynes and azides using the privileged scaffold of triterpenes have
been of interest for biological chemistry. Many publications deal with the synthesis of novel …

The synthesis of new fluorescent 2, 1, 3-benzothiadiazole-triazole-linked glycoconjugates is
described by a straightforward synthetic route, using a copper (I)-catalyzed azide–alkyne 1 …

In organic and inorganic synthesis and in analytical methods, an external conventional heat
source is usually applied to carry out a chemical reaction at a high temperature, or an …