Issue 37, 2015

Copper-catalysed azide–alkyne cycloadditions (CuAAC): an update

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.

Graphical abstract: Copper-catalysed azide–alkyne cycloadditions (CuAAC): an update

Article information

Article type
Review Article
Submitted
16 Jul 2015
Accepted
31 Jul 2015
First published
31 Jul 2015

Org. Biomol. Chem., 2015,13, 9528-9550

Copper-catalysed azide–alkyne cycloadditions (CuAAC): an update

E. Haldón, M. C. Nicasio and P. J. Pérez, Org. Biomol. Chem., 2015, 13, 9528 DOI: 10.1039/C5OB01457C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements