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 …

Traditional organic synthesis relies heavily on organic solvents for a multitude of tasks,
including dissolving the components and facilitating chemical reactions, because many …

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 …

The design of artificial catalysts able to compete with the catalytic proficiency of enzymes is
an intense subject of research. Non-covalent interactions are thought to be involved in …

The Huisgen 1, 3-dipolar cycloaddition reaction of organic azides and alkynes1, 2 has
gained considerable attention in recent years due to the introduction in 2001 of Cu (1) …

The metal catalyzed azide/alkyne 'click'reaction (a variation of the Huisgen 1, 3‐dipolar
cycloaddition reaction between terminal acetylenes and azides) has vastly increased in …

Asymmetric catalysis constitutes one of the most important subjects in chemistry originating
thousands of published works every year. But still, the application of such methodologies in …

In the last eight years, L-proline and L-proline derivatives, such as substituted prolinamides
or pyrrolidines, have been successfully used as organocatalysts in several reactions. In this …

The CuAAC “click” reaction has developed as one of the most useful and widely employed
reactions in ligation within polymer chemistry. This is due to the unique properties of the Cu …

Positive effects of the polymeric support on the performance of supported chiral catalysts, in
terms of activity, stability and selectivity–enantioselectivity, have been reported when the …