Issue 19, 2011
From the journal:

Chemical Communications

Nitrone-mediated radical coupling reactions: a new synthetic tool exemplified on dendrimer synthesis†

Edgar H. H. Wong,ab   Ozcan Altintas,a   Martina H. Stenzel,b   Christopher Barner-Kowollik*a  and  Tanja Junkers*c  

* Corresponding authors

a Preparative Macromolecular Chemistry, Institut für Technische Chemie und Polymerchemie, Karlsruhe Institute of Technology (KIT), Engesserstr. 18, 76128 Karlsruhe, Germany
E-mail: christopher.barner-kowollik@kit.edu
Fax: +49 721-60845740
Tel: +49 721-608-45641

b Centre for Advanced Macromolecular Design (CAMD), School of Chemical Engineering, The University of New South Wales, Sydney, NSW 2052, Australia

c Institute for Materials Research, Polymer Reaction Design Group, Universiteit Hasselt, Agoralaan, Gebouw D, B-3590 Diepenbeek, Belgium
E-mail: tanja.junkers@uhasselt.be
Fax: +32 1126-8399
Tel: +32 1126-8318

Abstract

A synthetic strategy employing nitrones as radical spin traps is presented on the example of the efficient generation of novel dendrimersvia a combination of radical and classical ‘click’ chemistry.

Graphical abstract: Nitrone-mediated radical coupling reactions: a new synthetic tool exemplified on dendrimer synthesis

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Article information

DOI
https://doi.org/10.1039/C1CC10322A
Article type
Communication
Submitted
17 Jan 2011
Accepted
16 Mar 2011
First published
11 Apr 2011

Chem. Commun., 2011,47, 5491-5493

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Nitrone-mediated radical coupling reactions: a new synthetic tool exemplified on dendrimer synthesis

E. H. H. Wong, O. Altintas, M. H. Stenzel, C. Barner-Kowollik and T. Junkers, Chem. Commun., 2011, 47, 5491 DOI: 10.1039/C1CC10322A

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