articleTop 1% cited
Copper-catalysed azide–alkyne cycloadditions (CuAAC): an update
Organic & Biomolecular Chemistry · 2015 · Vol. 13(37) · pp. 9528–9550
Estela Haldón(Universidad de Huelva)M. Carmen Nicasio✉(Universidad de Sevilla)Pedro J. Pérez✉(Comisión Sectorial de Investigación Científica)
Abstract
The reactions of organic azides and alkynes catalysed by copper species represent the prototypical examples of click chemistry. The so-called CuAAC reaction (copper-catalysed azide-alkyne cycloaddition), discovered in 2002, has been expanded since then to become an excellent tool in organic synthesis. In this contribution the recent results described in the literature since 2010 are reviewed, classified according to the nature of the catalyst precursor: copper(I) or copper(II) salts or complexes, metallic or nano-particulated copper and several solid-supported copper systems.
Click Chemistry and ApplicationsAdvanced biosensing and bioanalysis techniquesMonoclonal and Polyclonal Antibodies ResearchChemistryAzideAlkyneCopperCombinatorial chemistryCycloadditionClick chemistryCatalysisPolymer chemistryOrganic chemistry
Funding
- Consejería de Economía, Innovación, Ciencia y Empleo, Junta de Andalucía
- Ministerio de Economía y Competitividad
Citations
567
FWCI
25.10
field-weighted impact
References
288
Percentile
100%
vs. same field & year
Citations per year
References
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Polytriazoles as Copper(I)-Stabilizing Ligands in Catalysis
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