Issue 58, 2015
From the journal:

Chemical Communications

Correction: Combination of inverse electron-demand Diels–Alder reaction with highly efficient oxime ligation expands the toolbox of site-selective peptide conjugations

S. Hörner,a   C. Uth,a   O. Avrutina,a   H. Frauendorf,b   M. Wiesslerc  and  H. Kolmar*a  

* Corresponding authors

a Technische Universität Darmstadt, Clemens-Schöpf-Institut für Organische Chemie und Biochemie, Alarich-Weiss Straße 4, 64287 Darmstadt, Germany
E-mail: kolmar@biochemie-tud.de

b Georg-August-Universität Göttingen, Institut für Organische und Biomolekulare Chemie, Zentrale Analytik/Massenspektrometrie, Tammannstraße 2, 37077 Göttingen, Germany

c Deutsches Krebsforschungszentrum, Medizinische Physik in der Radiologie, Projektgruppe Biologische Chemie E020, Im Neuenheimer Feld, 69120 Heidelberg, Germany

Abstract

Correction for ‘Combination of inverse electron-demand Diels–Alder reaction with highly efficient oxime ligation expands the toolbox of site-selective peptide conjugations’ by S. Hörner, et al., Chem. Commun., 2015, DOI: 10.1039/c5cc03434e.

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Article information

DOI
https://doi.org/10.1039/C5CC90302E
Article type
Correction
Submitted
23 Jun 2015
Accepted
23 Jun 2015
First published
30 Jun 2015
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2015,51, 11727-11727

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Correction: Combination of inverse electron-demand Diels–Alder reaction with highly efficient oxime ligation expands the toolbox of site-selective peptide conjugations

S. Hörner, C. Uth, O. Avrutina, H. Frauendorf, M. Wiessler and H. Kolmar, Chem. Commun., 2015, 51, 11727 DOI: 10.1039/C5CC90302E

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