The ruthenium-catalyzed azide alkyne cycloaddition (RuAAC) affords 1, 5-disubstituted 1, 2,
3-triazoles in one step and complements the more established copper-catalyzed reaction …

Click Chemistry, a modular, rapid, and one of the most reliable tool for the regioselective 1,
2, 3‐triazole forming [3+ 2] reaction of organic azide and terimal alkyne is widely explored in …

α, α-Disubstituted piperidines and conformationally constrained polyhydroxylated
indolizidines bearing a hydroxymethyl substituent in position 8a were synthesized from a …

A Pd‐catalyzed highly selective tandem reaction of allenynes, aryl or alkenyl iodides, and
sodium azide for the synthesis of bicyclic 1, 2, 3‐triazole derivatives with a very broad …

Chemoselective transformations of functionalized sulfonyl fluorides and chlorides are
surveyed comprehensively. It is shown that sulfonyl fluorides provide an excellent selectivity …

A simple and efficient procedure was designed for the preparation of pyranoid glycals. In a
novel fashion, a series of protected glycopyranosyl bromides underwent reductive …

Synthesis of novel triazole fused iminocyclitol-δ-lactams is described. The synthetic
sequence involves the intermolecular [3+ 2] cycloaddition reaction of five-membered …

Triazoles have always occupied a pivotal position in the field of medicinal and
pharmaceutical chemistry. Recently, the area of chiral fused triazoles has gained attention …

The exploration of hybridization emerges as a potent tool in advancing drug discovery
research, with a significant emphasis on carbohydrate-containing hybrid scaffolds. Evidence …

Abstract In general, 1, 5-disubstituted 1, 2, 3-triazolyl moiety is much less common in the
synthesis and applications in comparison to its regioisomeric counterpart. Moreover, the …