Issue 2, 2015
From the journal:

Organic & Biomolecular Chemistry

Chiral recognition with a benzofuran receptor that mimics an oxyanion hole†

Ángel L. Fuentes de Arriba,a   Ángel Gómez Herrero,a   Omayra H. Rubio,a   Laura M. Monleón,a   Luis Simón Rubio, ORCID logo a   Victoria Alcázar,b   Francisca Sanzc  and  Joaquín R. Morán*a  

* Corresponding authors

a Organic Chemistry Department, Plaza de los Caídos 1-5, 37008 Salamanca, Spain
E-mail: romoran@usal.es
Fax: +34923294574
Tel: +34923294481

b Industrial Chemistry and Environmental Engineering Department, Jose Gutierrez Abascal 2, 28006 Madrid, Spain

c X-Ray Diffraction Service, Plaza de los Caídos 1-5, 37008 Salamanca, Spain

Abstract

A new chiral benzofuran receptor has been synthesized and its properties in the association of amino acid derivatives have been studied. X-ray structures were obtained and these corroborate the presence of an oxyanion-hole motif in these structures.

Graphical abstract: Chiral recognition with a benzofuran receptor that mimics an oxyanion hole

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Article information

DOI
https://doi.org/10.1039/C4OB01954G
Article type
Paper
Submitted
15 Sep 2014
Accepted
17 Oct 2014
First published
17 Oct 2014

Org. Biomol. Chem., 2015,13, 493-501

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Chiral recognition with a benzofuran receptor that mimics an oxyanion hole

Á. L. Fuentes de Arriba, Á. G. Herrero, O. H. Rubio, L. M. Monleón, L. Simón Rubio, V. Alcázar, F. Sanz and J. R. Morán, Org. Biomol. Chem., 2015, 13, 493 DOI: 10.1039/C4OB01954G

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