Issue 14, 2006
From the journal:

Chemical Communications

Synthesis, stability and optimized photolytic cleavage of 4-methoxy-2-nitrobenzyl backbone-protected peptides†

Erik C. B. Johnsona  and  Stephen B. H. Kent*a  

* Corresponding authors

a Institute for Biophysical Dynamics, Department of Biochemistry and Molecular Biology, and Department of Chemistry, The University of Chicago, 920 East 58th Street, Chicago, USA
E-mail: skent@uchicago.edu
Fax: 773-702-0439
Tel: 773-702-4912

Abstract

We demonstrate the potential of 4-methoxy-2-nitrobenzyl as a Boc chemistry-compatible fully reversible backbone modification for synthetic peptides.

Graphical abstract: Synthesis, stability and optimized photolytic cleavage of 4-methoxy-2-nitrobenzyl backbone-protected peptides

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Article information

DOI
https://doi.org/10.1039/B600304D
Article type
Communication
Submitted
10 Jan 2006
Accepted
13 Feb 2006
First published
02 Mar 2006

Chem. Commun., 2006, 1557-1559

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Synthesis, stability and optimized photolytic cleavage of 4-methoxy-2-nitrobenzyl backbone-protected peptides

E. C. B. Johnson and S. B. H. Kent, Chem. Commun., 2006, 1557 DOI: 10.1039/B600304D

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