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 …

Click chemistry is an approach that uses efficient and reliable reactions, such as Cu (I)-
catalyzed azide–alkyne cycloaddition (CuAAC), to bind two molecular building blocks …

Click chemistry is a concept in which modular synthesis is used to rapidly find new
molecules with desirable properties. Copper (i)-catalysed azide–alkyne cycloaddition …

Unactivated olefins are converted to alkyl azides with bench-stable NaN3 in the presence of
FeCl3· 6H2O under blue-light irradiation. The products are obtained with anti-Markovnikov …

An efficient and improved procedure for the preparation of aromatic azides and their
application in the Cu (I)-catalyzed azide− alkyne 1, 3-dipolar cycloaddition (“click reaction”) …

The discovery of new methods for stereoselective glycoside synthesis and convergent
oligosaccharide assembly has been critical for the area of glycosciences. At the heart of this …

A one-pot reaction for Cu (II)-catalyzed diazo transfer and Cu (I)-catalyzed azide− alkyne 1,
3-dipolar cycloaddition (sometimes called click reaction) is reported. 1, 4-Disubstituted 1, 2 …

Cycloaddition is an essential tool in chemical synthesis. Instead of using light or heat as a
driving force, marine sponges promote cycloaddition with a more versatile but poorly …

Exploring potent adjuvants and new vaccine strategies is crucial for the development of
protein vaccines. In this work, we synthesized a new TLR4 agonist, structurally simplified …

As part of ongoing activities toward the design of potent and selective ligands against
galactoside‐binding proteins from animal, bacterial, and plant lectins, a systematic …