Green (sustainable) chemistry provides a framework for chemists, pharmacists, medicinal
chemists and chemical engineers to design processes, protocols and synthetic …

Oxidative strategies are a powerful tool in organic synthesis for the formation of heteroatom–
heteroatom, carbon–heteroatom, and carbon–carbon bonds. Among these processes the …

An electrochemical intermolecular dehydrogenative coupling reaction of isothiocyanates
with 2‐aminopyridines/amidines was developed. Using n‐Bu4NI as the catalyst and …

A strategy for the synthesis of quinazolines via elemental sulfur‐mediated oxidative
condensation of nitriles and 2‐(aminomethyl) anilines was developed. The reaction was …

A new 'one pot'tandem synthesis of 2-substituted benzimidazoles has been developed from
2-aminobenzyl alcohol/2-aminobenzamide and different coupling partners (nitriles …

Given their two reactive centers, thioamides serve as useful synthetic building blocks for
more complex heterocyclic molecules. The reaction of pyridine-4-thiocarboxamide (1) and …

A simple and facile catalyst-free method for the construction of α-thioacrylic acids has been
developed from readily-available aryl alkynoates and thiols at room temperature. Various α …

In the present manuscript, we report serendipitous synthesis of 3, 5-diaryl-1, 2, 4-
thiadiazoles with the aid of a household compact fluorescent lamp (CFL). In presence of α …

A simple and practical method for the one‐pot synthesis of 3‐aryl‐5‐amino‐1, 2, 4‐
thiadiazoles from imidates and thioureas has been developed. The protocol proceeds …

Thiadiazole moieties are present in many natural products and pharmaceutical compounds
that possess a broad spectrum of biological activities, serving as antidepressant, anxiolytic …