Enamines exhibit exceptionally high reactivity in their 1, 3‐dipolar cycloaddition reactions
with azides in comparison with other dipolarophiles. This review includes the reactions of …

The development of metal‐free syntheses toward 1, 2, 3‐triazoles has been a burgeoning
research area throughout the past decade. Despite the numerous advances, the scarceness …

An overview of the latest developments in the metal-free synthesis of non-benzo-fused N-
functionalized and NH-1, 2, 3-triazoles is provided in this feature article. Synthetic studies …

To develop antiviral therapeutics against human coronavirus (HCoV) infections, suitable
coronavirus drug targets and corresponding lead molecules must be urgently identified …

A metal-free three-step synthesis toward functionalized 1-methyleneisoquinolines from
readily available substrates is reported. First, acetal-containing 1, 2, 3-triazoles were …

An efficient access to the novel 5-(het) arylamino-1, 2, 3-triazole derivatives has been
developed. The method is based on Buchwald–Hartwig cross-coupling reaction of 5-Amino …

A typical Cobalt‐Copper ferrite nanoparticles (CoCuFe2O4) was used as a catalyst for one‐
pot [3+ 2] cycloaddition of alkyl azides with alkynes at room temperature in green media …

A new metal-free one-pot three-component procedure towards fully substituted
triazolochromenes has been developed, starting from commercially available materials …

A reaction of equimolar equivalents of 1-(4-methoxyphenyl)-5-methyl-1 H-1, 2, 3-triazole-4-
carbohydrazide (1) and indoline-2, 3-dione (2) in boiling ethanol for 4 h under acidic …

A novel series of 1, 2, 3-triazolo-fused allocolchicine analogs is described. The strategy to
prepare these analogs involves two steps: The first step is the synthesis of 1, 2, 3-triazole …