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Preparation of Peptide o-Aminoanilides Using a Modified Dawson's Linker for Microwave-Assisted Peptide Synthesis

Synlett
DOI: 10.1055/s-0036-1588862



Based on the structure of Dawson’s 3,4-diaminobenzoic acid (Dbz) linker designed for Fmoc solid-phase peptide-thioester synthesis, the 4-amino-3-nitrobenzoic acid [Dbz(NO2)] linker was developed for microwave-assisted synthesis. The Dbz(NO2) linker can be readily converted into the Dbz linker by on-resin reduction with SnCl2 after construction of the protected peptide resin. Although epimerization of C-terminal amino acid restricts the use of Dbz(NO2) linker to the synthesis of peptide-Gly-thioester, use of this linker can prevent side reactions that arise when Dbz or Dbz(Aloc) linkers are used in the microwave-assisted synthesis of Gly-rich peptides.
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© Georg Thieme Verlag Stuttgart · New York

Artikel in Thieme eJournals:
Inhaltsverzeichnis  |  Abstract  |  Volltext

Authors:   Shugo Tsuda; Tsuyoshi Uemura; Masayoshi Mochizuki; Hideki Nishio; Taku Yoshiya
Journal:   Synlett
Volume:   9
edition:   eFirst
Year:   2017
Pages:   1166
DOI:   10.1055/s-0036-1588862
Publication date:   21-Jun-2017
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