Epimerization-Free Synthesis of Azo-Substituted Di- and Tripeptides by Cross-Coupling of O-Triflated Derivatives and Diazenyl Anion Equivalents

Abstract Based on our previous work, a method for the synthesis of azo-substituted small peptides through C(sp2)–N(sp2) cross-coupling between triflated peptide derivatives and N-aryl-N′-trimethylsilyldiazenes is reported. The peptide-substituted azobenzene products are formed in acceptable yields with full stereoretention at the asymmetrically substituted carbon atom despite the basic reaction medium.

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Publication Details

Journal
Synthesis
Published
2025-11-26
DOI
https://doi.org/10.1055/a-2756-7473
Primary Topic
Chemical Synthesis and Analysis
Type
article
Field-Weighted Citation Impact
0.00
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article

Epimerization-Free Synthesis of Azo-Substituted Di- and Tripeptides by Cross-Coupling of O-Triflated Derivatives and Diazenyl Anion Equivalents

Martin Oestreich, Wolfgang Obermayer, Kezhuo Zhang, Jon B. Hagen
Synthesis
Chemical Synthesis and Analysis
article

Epimerization-Free Synthesis of Azo-Substituted Di- and Tripeptides by Cross-Coupling of O-Triflated Derivatives and Diazenyl Anion Equivalents

Martin Oestreich, Wolfgang Obermayer, Kezhuo Zhang, Jon B. Hagen
article en

Abstract

Abstract Based on our previous work, a method for the synthesis of azo-substituted small peptides through C(sp2)–N(sp2) cross-coupling between triflated peptide derivatives and N-aryl-N′-trimethylsilyldiazenes is reported. The peptide-substituted azobenzene products are formed in acceptable yields with full stereoretention at the asymmetrically substituted carbon atom despite the basic reaction medium.

SynthesisVol. 58(07)
Technische Universität Berlin (DE)
Openalex Percentile: Top 67%
Chemical Synthesis and Analysis
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