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 …

The research on 1, 2, 3-triazoles has been lively and ever-growing since its stimulation by
the advent of click chemistry. The attractiveness of 1H-1, 2, 3-triazoles and their derivatives …

1, 2, 3-Triazole scaffolds are not obtained in nature, but they are still intensely investigated
by synthetic chemists in various fields due to their excellent properties and green synthetic …

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

A p-TsOH-mediated 1, 3-dipolar cycloaddition of nitroolefins and sodium azide for the
synthesis of 4-aryl-NH-1, 2, 3-triazoles has been developed. p-TsOH was discovered as a …

Abstract An organocatalytic azide–aldehyde [3+ 2] cycloaddition (organo‐click) reaction of a
variety of enolizable aldehydes is reported. The organo‐click reaction is characterized by a …

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 …

A general strategy was developed for the synthesis of new fully decorated 1, 2, 3-triazoles
(5a-m & 6a-e) containing coumarine and sulfonyl-benzimidazole from 3-(2-((1-methyl-1H …

Copper (I)-catalyzed azide–alkyne cycloaddition (CuAAC) is an essential “click chemistry”
reaction that is widely used in chemical biology, medicinal chemistry and materials science …

The present feature article describes the different organocatalytic routes for the synthesis of
substituted 1, 2, 3-triazoles. This methodology has recently gained much attention due to its …