Issue 9, 2001
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Unusually facile palladium catalysed oxidation of imidazolidines and oxazolidines

Alexandre Alexakis,*a   Isabelle Aujard,b   Julien Pytkowicz,b   Sylvain Rolandb  and  Pierre Mangeney*b  

* Corresponding authors

a Department of Organic Chemistry, University of Geneva, 30 quai Ernest Ansermet, Genève 4, Switzerland
E-mail: alexandre.alexakis@chiorg.unige.ch
Fax: Fax (int.) +41 22 328 73 96
Tel: Tel. +41 22 702 65 22

b Laboratoire de Chimie des Organoéléments, UMR 7611, Université Pierre et Marie Curie, 4 place Jussieu, Paris Cedex 05, France

Abstract

An unusually facile palladium catalysed oxidation of imidazolidines is described, affording in good yield, the monoamide of the corresponding diamine or the corresponding imidazolines. Oxazolidines derived from ephedrine react similarly.

Graphical abstract: Unusually facile palladium catalysed oxidation of imidazolidines and oxazolidines

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Article information

DOI
https://doi.org/10.1039/B010089G
Article type
Communication
Submitted
11 Dec 2000
Accepted
03 Apr 2001
First published
18 Apr 2001

J. Chem. Soc., Perkin Trans. 1, 2001, 949-951

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Unusually facile palladium catalysed oxidation of imidazolidines and oxazolidines

A. Alexakis, I. Aujard, J. Pytkowicz, S. Roland and P. Mangeney, J. Chem. Soc., Perkin Trans. 1, 2001, 949 DOI: 10.1039/B010089G

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