Copper (I)-catalyzed 1, 3-dipolar cycloaddition between organic azides and terminal
alkynes, commonly known as CuAAC or click chemistry, has been identified as one of the …

Cu (I)-catalyzed azide–alkyne 1, 3-dipolar cycloaddition (CuAAC), popularly known as the
“click reaction”, serves as the most potent and highly dependable tool for facile construction …

Despite enormous progress in the field of the synthetic chemistry involving, for example,
catalytic and combinatorial synthesis of a large libraries of compounds, multicomponent …

The glycosyl 1, 2, 3-triazoles are expediently accessible from readily available sugar-
derived glycosyl azide by utilizing modular CuAAC “Click Chemistry”, and the resulting …

Glycosyl triazoles are conveniently accessible and contain multiple metal-binding units that
may assist in metal-mediated catalysis. Azide derivatives of d-glucose have been converted …

There is an increasing demand for significant amount of carbohydrate‐containing molecules
owing to their complete chemical, biological, and pharmacological investigations to better …

Tris (pentafluorophenyl) borane-promoted stereoselective glycosylation with
trichloroacetimidate glycosyl donors is described. The reactions proceed efficiently with a …

The synthesis of triazolyl azido alcohols from terminal alkyne via oxirane ring-opening of
epichlorohydrin, followed by click reaction with alkynes, and subsequent azidation of …

In the last two decades, click chemistry has progressed as a powerful tool in joining two
different molecular units to generate fascinating structures with a widespread application in …

The C–C triple bond of phenylacetylene undergoes the anti-Markovnikov addition of the Rh–
H bond of RhH {κ3-P, O, P-[xant (PiPr2) 2]}(1; xant (PiPr2) 2= 9, 9-dimethyl-4, 5-bis …