1, 2, 3-triazoles represent a functional heterocyclic core that has been at the center of
modern organic chemistry since the beginning of click chemistry. Being a versatile …

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 …

Since the beginning of click chemistry, 1, 2, 3-triazoles has been at the center of modern
organic chemistry. This versatile framework has found broad applications in organic …

Reactions of 1-(5-methyl)-1 H-1, 2, 3-triazol-4-yl) ethan-1-ones and benzaldehydes in
ethanol under basic conditions gave the corresponding chalcones. Reactions of the …

Nitrogen (N) fertilisers amended with nitrification inhibitors can increase nitrogen use
efficiencies in agricultural systems but the effectiveness of existing commercial inhibitor …

Recently, 1, 4-disubstituted 1, 2, 3-triazoles were reported by us as a new class of
nitrification inhibitors, which can outperform the commercial compound 3, 4 …

A pyridone-derived phosphate prodrug of an enhancer of zeste homolog 2 (EZH2) inhibitor
was designed and synthesized to improve the inhibitor's aqueous solubility. This prodrug …

A molecular iodine mediated condensation–cyclization reaction for the synthesis of 4‐aryl‐
NH‐1, 2, 3‐triazoles has been developed from readily available α‐azido acetophenones …

Cu (I)-catalyzed azide− alkyne 1, 3-dipolar cycloaddition (CuAAC)-commonly known as the
“click reaction”-serves as the most effective and highly reliable tool for facile construction of …

Herein, we report a rapid, one-step synthesis of α-ketoacetals via electrophilic etherification
of α-alkoxy enolates and monoperoxyacetals. Methyl, primary, and secondary α-ketoacetals …