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

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) …

After an initial period of validating asymmetric organocatalysis by using a wide range of
important model reactions that constitute the essential tools of organic synthesis, the time …

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 …

Nach einer ersten Phase orientierender Studien zur asymmetrischen Organokatalyse, die
vornehmlich der Untersuchung wichtiger Modellreaktionen der organischen Synthese …

A new tris (1-benzyl-1 H-1, 2, 3-triazol-4-yl) methanol ligand 3 has been prepared by a triple
Cu (I)-catalyzed alkyne− azide 1, 3-dipolar cycloaddition (CuAAC). Ligand 3 forms a stable …

The development of a highly efficient, polymer-supported organocatalyst for the Michael
addition of ketones to nitroolefins is described. A 1, 2, 3-triazole ring, constructed through a …

Organocatalytic asymmetric α-oxidation and amination reactions of carbonyl compounds are
highly useful synthetic methodologies, especially in generating chiral building blocks that …