Synfacts 2026; 22(01): 94
DOI: 10.1055/a-2738-9078
Peptide Chemistry

Ugi Reaction for the Synthesis of Di- and Tripeptides

Authors

Hatam M, Tehranfar D, Martens J *. Universität Oldenburg, Germany
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

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