Issue 82, 2013
From the journal:

Chemical Communications

Highly diastereoselective radical cyclisations of chiral sulfinimines†

Elise M. Rochette,a   William Lewis,a   Al G. Dossetterb  and  Robert A. Stockman*a  

* Corresponding authors

a School of Chemistry, University of Nottingham, Nottingham, UK
E-mail: Robert.stockman@nottingham.ac.uk

b AstraZeneca, Alderley Park, Macclesfield, UK

Abstract

Chiral amines are formed by the highly diastereoselective intramolecular addition of alkyl and aryl radicals onto chiral mesityl sulfinimines.

Graphical abstract: Highly diastereoselective radical cyclisations of chiral sulfinimines

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Article information

DOI
https://doi.org/10.1039/C3CC45452E
Article type
Communication
Submitted
18 Jul 2013
Accepted
22 Aug 2013
First published
22 Aug 2013
This article is Open Access
Creative Commons BY license

Chem. Commun., 2013,49, 9395-9397

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Highly diastereoselective radical cyclisations of chiral sulfinimines

E. M. Rochette, W. Lewis, A. G. Dossetter and R. A. Stockman, Chem. Commun., 2013, 49, 9395 DOI: 10.1039/C3CC45452E

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