Azides are important intermediates in organic synthesis. They can function as precursors to
form amines, amides, quinolones, pyridines, triazoles, amidines, indoles, and so on …

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 …

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 …

An unprecedented approach that enables the direct and selective preparation of 1, 5-
disubstituted 1, 2, 3-triazoles from abundantly available building blocks such as primary …

NH-1, 2, 3-Triazole moieties are a part of the design of various biologically active
compounds, pharmaceutical agents and functional materials. Unfortunately, the applications …

As the search for competent soft-Lewis basic complexants for separations continues to
evolve toward identification of a chemoselective moiety for speciation of the minor actinides …

A metal‐free three‐component coupling of α‐CF3 carbonyls, azides and amines for the
regioselective synthesis of 1, 4, 5‐trisubstituted 1, 2, 3‐triazoles in the air is established …

An efficient synthetic route for the construction of N 2-aryl 1, 2, 3-triazoles is reported via
sequential C–N bond formation and electro-oxidative N–N coupling under metal-free …

A formal [3+ 3] cycloaddition reaction between azides and in situ formed azaoxyallyl cations
has been realized. This reaction provided an efficient and practical pathway to synthesize 1 …

Organocatalytic enamine–azide [3+ 2] cycloadditions between β-keto sulfones and aryl
azides can be performed at room temperature in good to excellent yields of products in the …