Triazoles are important five-membered heterocyclic scaffold due to their extensive biological
activities. This framework can be readily obtained in good to excellent yields on the …

Immediately after the invention of 'Click Chemistry'in 2002, the regioselective 1, 2, 3-triazole
scaffolds resulted from respective organic azides and terminal alkynes under Cu (I) catalysis …

A metal‐free three‐component reaction to synthesize 1, 4, 5‐trisubstituted 1, 2, 3‐triazoles
from readily available building blocks, such as aldehydes, nitroalkanes, and organic azides …

Metal-free 1, 3-dipolar cycloaddition reactions have proven to be a powerful tool for the
assembly of key heterocycles, in particular diversely functionalized 1, 2, 3-triazoles. A …

A synthetically useful approach to functionalized triazoles is described via the reaction of β-
carbonyl phosphonates and azides. 1, 4-and 1, 5-disubstituted and 1, 4, 5-trisubstituted …

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 …

Abstract A novel organocatalyzed [3+ 2] cycloaddition reaction of nitroolefins with glycosyl
azides as well as organic azides has been developed for successful construction of 1, 5 …

A simple and efficient metal-free methodology for the regioselective synthesis of 1, 4-
disubstituted-1, 2, 3-triazoles has been developed by applying a novel inverse electron …

Its even more than a centennial that the systematic researches of chemical alteration of
sugars have been advancing. Out of all the interest in the field of N‐glycoside has …

Organocatalytic 1,3-dipolar cycloaddition reaction of α,β-unsaturated ketones with azides
through iminium catalysis - Green Chemistry (RSC Publishing) DOI:10.1039/C4GC01929F …