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 …

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) …

Applications for advanced functional soft materials that possess precisely engineered
properties and functional groups have been expanding significantly with the development of …

The modification of polymers after the successful achievement of a polymerization process
represents an important task in macromolecular science. Cycloaddition reactions, among …

In 2001, Sharpless and co‐workers introduced “click” chemistry, a new approach in organic
synthesis that involves a handful of almost perfect chemical reactions. Among these carefully …

The present advances in biology are related to progress in genomics, proteomics, and other
“-omics”, including glycomics, working with a large amount of data regarding human and …

Surface plasmon resonance (SPR)-based biosensors are very powerful tools for the study of
biomolecular interactions, chemical detection and immunoassays. This paper reviews the …

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 …

The increasing need for materials with tightly controlled structures will continue to fuel the
induction of synthetic organic concepts into materials science. One powerful example is the …