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

Author:

Tsuda Shugo1,Yoshiya Taku1ORCID,Uemura Tsuyoshi1,Mochizuki Masayoshi1,Nishio Hideki12

Affiliation:

1. Peptide Institute, Inc.

2. Graduate School of Science, Osaka University

Abstract

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.

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry

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