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Novel N,S-Phenacyl Protecting Group and Its Application for Peptide Synthesis
Abstract The phenacyl group can be introduced onto amino and thio groups by N,S-alkylation reactions. Conversely, these groups are removed rapidly by employing magnesium in acetic acid. This protecting group was successfully applied to a short peptide synthesis of Boc-L-Cys-Gly-OMe.
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Published in: | Synlett 2008-07, Vol.2008 (12), p.1907-1909 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Abstract
The phenacyl group can be introduced onto amino and thio groups
by N,S-alkylation reactions. Conversely, these groups are removed
rapidly by employing magnesium in acetic acid. This protecting group
was successfully applied to a short peptide synthesis of Boc-L-Cys-Gly-OMe. |
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ISSN: | 0936-5214 1437-2096 |
DOI: | 10.1055/s-2008-1077887 |