Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5271343 | Tetrahedron Letters | 2014 | 5 Pages |
Abstract
In this study, the potential of N-alkoxymethyl groups as protectants for the peptide backbone has been investigated. These groups were found to be compatible with the standard conditions of Fmoc/tBu SPPS, and can be cleaved off from the peptide backbone by acids. Thus, backbone N-alkoxymethyl groups may be useful to prevent undesired side-reactions and/or interchain aggregation during peptide elongation on the solid-phase. However, the main issue for their application as protecting groups is the difficulty to incorporate them into the peptide backbone.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ana I. Fernández-Llamazares, Jan Spengler, Fernando Albericio,