Issue 24, 2004
From the journal:

Organic & Biomolecular Chemistry

Synthesis of a silk-inspired peptide–oligothiophene conjugate†

Harm-Anton Klok,*a   Annette Rösler,b   Günther Götz,c   Elena Mena-Osteritzc  and  Peter Bäuerle*c  

* Corresponding authors

a École Polytechnique Fédérale de Lausanne, Institut des Matériaux, Laboratoire des Polymères, Bâtiment MX-D, Lausanne, Switzerland
E-mail: Harm-Anton.Klok@epfl.ch

b Max Planck Institute for Polymer Research, Ackermannweg 10, Mainz, Germany

c Department of Organic Chemistry II, University of Ulm, Albert-Einstein-Allee 11, Ulm, Germany
E-mail: Peter.Baeuerle@chemie.uni-ulm.de

Abstract

The first example of an oligothiophene–peptide conjugate, which was obtained by solid-phase acylation of a resin-bound silk-inspired oligopeptide sequence with a carboxylic acid functionalized regioregular tetra(3-hexylthiophene) derivative, is reported.

Graphical abstract: Synthesis of a silk-inspired peptide–oligothiophene conjugate

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Article information

DOI
https://doi.org/10.1039/B415454A
Article type
Communication
Submitted
06 Oct 2004
Accepted
10 Oct 2004
First published
08 Nov 2004

Org. Biomol. Chem., 2004,2, 3541-3544

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Synthesis of a silk-inspired peptide–oligothiophene conjugate

H. Klok, A. Rösler, G. Götz, E. Mena-Osteritz and P. Bäuerle, Org. Biomol. Chem., 2004, 2, 3541 DOI: 10.1039/B415454A

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