Issue 34, 2008
From the journal:

Chemical Communications

Highly diastereoselective self-assembly of chiral tris(m-ureidobenzyl)amino capsules†

Mateo Alajarín,*a   Aurelia Pastor,*a   Raúl-Angel Orenes,a   Andres E. Goetab  and  Jonathan W. Steedb  

* Corresponding authors

a Departamento de Química Orgánica, Facultad de Química, Universidad de Murcia. Campus de Espinardo, Murcia, Spain
E-mail: alajarin@um.es; aureliap@um.es
Fax: +34 968 364149
Tel: +34 968 367497

b Department of Chemistry, University of Durham, University Science Laboratories, South Road, Durham, UK

Abstract

The self-assembly of chiral tris(m-ureidobenzyl)amines to give dimeric capsules is a highly diastereoselective process in solution, while in the solid state, the formation of the corresponding capsules is not only diastereoselective but also regioselective.

Graphical abstract: Highly diastereoselective self-assembly of chiral tris(m-ureidobenzyl)amino capsules

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Article information

DOI
https://doi.org/10.1039/B809835B
Article type
Communication
Submitted
13 Jun 2008
Accepted
08 Jul 2008
First published
25 Jul 2008

Chem. Commun., 2008, 3992-3994

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Highly diastereoselective self-assembly of chiral tris(m-ureidobenzyl)amino capsules

M. Alajarín, A. Pastor, R. Orenes, A. E. Goeta and J. W. Steed, Chem. Commun., 2008, 3992 DOI: 10.1039/B809835B

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