Subscribe to RSS
DOI: 10.1055/a-2738-9078
Ugi Reaction for the Synthesis of Di- and Tripeptides
Authors
Single-Step Synthesis of Racemic Di- and Tripeptides Derived from Unnatural β-Hydroxy and β-Mercapto α-Amino Acids by the Ugi Reaction.
Synthesis 1994; 619-623
DOI: 10.1055/s-1994-25535

Significance
The Ugi reaction is a multicomponent reaction and is used for the synthesis of a reactive building block in synthetic organic chemistry. In this study, the authors developed a step-economic Ugi reaction for the synthesis of di- and tripeptides using unnatural β-hydroxy and β-mercapto α-amino acids.
Comment
The developed Ugi reaction uses the imine component derived from spiro 3-thiazolines or oxazolines, isocyanates, and amino acid carboxylates for the synthesis of oligopeptides in good yields. This method is a simple and single-step reaction for the synthesis of oligopeptides.
Publication History
Article published online:
16 December 2025
© 2025. Thieme. All rights reserved.
Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany
