Issue 22, 2006
From the journal:

Chemical Communications

The “triamino-analogue” of methyl allocholate; a rigid, functionalised scaffold for supramolecular chemistry†

Khadga M. Bhattarai,a   Vicente del Amo,a   Germinal Magro,a   Adam L. Sisson,a   Jean-Baptiste Joos,a   Jonathan P. H. Charmant,a   Anob Kantachaa  and  Anthony P. Davis*a  

* Corresponding authors

a School of Chemistry, University of Bristol, Cantock's Close, Bristol, UK
E-mail: Anthony.Davis@bristol.ac.uk
Fax: +44 117 9298611
Tel: +44 117 9546334

Abstract

Cholic acid 1 has been converted into triamine 5 with the all-trans polycyclic allocholanoyl skeleton and co-directed, axial amino groups; the potential of this system as a scaffold is illustrated by conversion to a preorganised anion receptor.

Graphical abstract: The “triamino-analogue” of methyl allocholate; a rigid, functionalised scaffold for supramolecular chemistry

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Article information

DOI
https://doi.org/10.1039/B602415G
Article type
Communication
Submitted
17 Feb 2006
Accepted
02 May 2006
First published
15 May 2006

Chem. Commun., 2006, 2335-2337

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The “triamino-analogue” of methyl allocholate; a rigid, functionalised scaffold for supramolecular chemistry

K. M. Bhattarai, V. del Amo, G. Magro, A. L. Sisson, J. Joos, J. P. H. Charmant, A. Kantacha and A. P. Davis, Chem. Commun., 2006, 2335 DOI: 10.1039/B602415G

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