Issue 6, 2005
From the journal:

Chemical Communications

Design and synthesis of a new class of arginine analogues with an improved anion binding site in the side chain†

Carsten Schmuck*a  and  Lars Geigera  

* Corresponding authors

a Institut für Organische Chemie, Universität Würzburg, Am Hubland, Würzburg, Germany
E-mail: schmuck@chemie.uni-wuerzburg.de
Fax: + 49 931 8884625
Tel: + 49 931 8885326

Abstract

Replacing the guanidinium group in arginine (1) by a guanidiniocarbonyl pyrrole moiety provides a new class of artificial amino acids (2), that can be used as building blocks in standard solid phase peptide synthesis.

Graphical abstract: Design and synthesis of a new class of arginine analogues with an improved anion binding site in the side chain

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Article information

DOI
https://doi.org/10.1039/B415543B
Article type
Communication
Submitted
07 Oct 2004
Accepted
09 Nov 2004
First published
21 Dec 2004

Chem. Commun., 2005, 772-774

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Design and synthesis of a new class of arginine analogues with an improved anion binding site in the side chain

C. Schmuck and L. Geiger, Chem. Commun., 2005, 772 DOI: 10.1039/B415543B

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