Issue 9, 2004
From the journal:

Chemical Communications

Synthesis and resolution of the planar chirality of ester-functionalised phospharuthenocenes

Duncan Carmichael,*a   Jürgen Klankermayer,a   Louis Ricarda  and  Nicolas Seebotha  

* Corresponding authors

a CNRS UMR 7653, DCPH Ecole Polytechnique, 91128 Palaiseau cedex, France
E-mail: Duncan.Carmichael@polytechnique.fr
Fax: + 33 1 69333990
Tel: + 33 1 69334571

Abstract

Menthyl phospholide ester anions provide an operationally simple and high yielding entry to the first planar chiral enantiopure phospharuthenocene derivatives.

Graphical abstract: Synthesis and resolution of the planar chirality of ester-functionalised phospharuthenocenes

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Article information

DOI
https://doi.org/10.1039/B401088D
Article type
Communication
Submitted
23 Jan 2004
Accepted
12 Mar 2004
First published
14 Apr 2004

Chem. Commun., 2004, 1144-1145

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Synthesis and resolution of the planar chirality of ester-functionalised phospharuthenocenes

D. Carmichael, J. Klankermayer, L. Ricard and N. Seeboth, Chem. Commun., 2004, 1144 DOI: 10.1039/B401088D

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