Issue 12, 2009

1,2-Dimethylindole-3-sulfonyl (MIS) as protecting group for the side chain of arginine

Abstract

The protection of arginine (Arg) side chains is a crucial issue in peptide chemistry because of the propensity of the basic guanidinium group to produce side reactions. Currently, sulfonyl-type protecting groups, such as 2,2,5,7,8-pentamethylchroman (Pmc) and 2,2,4,6,7-pentamethyldihydrobenzofurane (Pbf), are the most widely used for this purpose. Nevertheless, Arg side chain protection remains problematic as a result of the acid stability of these two compounds. This issue is even more relevant in Arg-rich sequences, acid-sensitive peptides and large-scale syntheses. The 1,2-dimethylindole-3-sulfonyl (MIS) group is more acid-labile than Pmc and Pbf and can therefore be a better option for Arg side chain protection. In addition, MIS is compatible with tryptophan-containing peptides.

Graphical abstract: 1,2-Dimethylindole-3-sulfonyl (MIS) as protecting group for the side chain of arginine

Supplementary files

Article information

Article type
Paper
Submitted
09 Mar 2009
Accepted
16 Mar 2009
First published
23 Apr 2009

Org. Biomol. Chem., 2009,7, 2565-2569

1,2-Dimethylindole-3-sulfonyl (MIS) as protecting group for the side chain of arginine

A. Isidro, D. Latassa, M. Giraud, M. Álvarez and F. Albericio, Org. Biomol. Chem., 2009, 7, 2565 DOI: 10.1039/B904836G

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