The copper‐catalyzed alkyne‐azide cycloaddition (CuAAC) is a highly versatile,
regioselective synthesis of 1, 4‐disubstituted 1, 2, 3‐triazoles under mild reaction conditions …

Heterocyclic compounds, both naturally derived and synthetically produced, constitute a
wide variety of biologically active and industrially important compounds. The synthesis and …

The preparation and full characterization of a variety of mono-([L1-H]), di-([L2-H2],[L2A-H2]),
and tri-([L3-H3]) 1, 2, 3-triazolium salts constructed form “clicked” hydroxybenzene …

Iodide (I–) is an essential micronutrient for thyroid function. Hence, rapid and portable
sensing is important for I–quantification in food and biological samples. Herein, we report …

A series of new mono-1, 2, 3-triazole derivatives of pyrimidine nucleobases were
synthesized by one-pot copper (I)-catalyzed 1, 3-dipolar cycloaddition reactions between N …

Following a copper catalyzed alkyne azide cycloaddition (CuAAC) and N-alkylation
protocols, we report the preparation of a hybrid N-heterocyclic/mesoionic [NHC (H+)-MIC …

In this study a series of new benzimidazolium salts (2a–c) were synthesized from the
reaction of 5, 6-dimethyl-1-(alkylbenzyl)-1H-benzo [d] imidazole with various alkyl halides …

Reaction of triazolium precursors [MIC (CH2) n‐H+] I−(n= 1–3) with potassium
hexamethyldisilazane (KHMDS) and AuCl (SMe2) generates the gold (I) complexes of the …

We report the preparation and full characterization of a series of hydroxyl functionalized 1, 2,
3-triazolylidene-based PEPPSI complexes 2a–c and their catalytic application in the Suzuki …

The efficient synthesis of O-and S-functionalized 1, 2, 3-triazoliums is reported. Owing to
their physical properties, these cations are efficient ionic liquids for Baylis–Hillman addition …