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Copper-catalyzed azide-alkyne cycloaddition (CuAAC) and beyond: new reactivity of copper(I) acetylides

Academic Article
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Overview

authors

  • Hein, J. E.
  • Fokin, Valery

publication date

  • 2010

journal

  • Chemical Society Reviews  Journal

abstract

  • Copper-catalyzed azide-alkyne cycloaddition (CuAAC) is a widely utilized, reliable, and straightforward way for making covalent connections between building blocks containing various functional groups. It has been used in organic synthesis, medicinal chemistry, surface and polymer chemistry, and bioconjugation applications. Despite the apparent simplicity of the reaction, its mechanism involves multiple reversible steps involving coordination complexes of copper(I) acetylides of varying nuclearity. Understanding and controlling these equilibria is of paramount importance for channeling the reaction into the productive catalytic cycle. This tutorial review examines the history of the development of the CuAAC reaction, its key mechanistic aspects, and highlights the features that make it useful to practitioners in different fields of chemical science.

subject areas

  • Alkynes
  • Azides
  • Catalysis
  • Copper
  • Cyclization
  • Iodine
  • Sulfones
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Identity

PubMed Central ID

  • PMC3073167

International Standard Serial Number (ISSN)

  • 0306-0012

Digital Object Identifier (DOI)

  • 10.1039/b904091a

PubMed ID

  • 20309487
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Additional Document Info

start page

  • 1302

end page

  • 1315

volume

  • 39

issue

  • 4

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