The Ugi-Joullié three-component (UJ-3CR) and related reactions. Recent developments, mechanistic aspects and synthesis of natural products and bioactive compounds

Abstract

The Ugi-Joullié three-component reaction evolved from the classic Ugi four-component reaction and enables the facile and efficient formation of polysubstituted nitrogen heterocycles from cyclic imines, isonitriles and carboxylic acids. Recent progress in the field aimed to expand its scope is reviewed, with emphasis in the development of new variations and substrates, and the acquisition of insights on relevant mechanistic aspects of this reaction. Its application to the synthesis of natural products, their analogs and bioactive compounds are also discussed.

Article information

Article type
Review Article
Submitted
30 Dec 2025
Accepted
11 Feb 2026
First published
12 Feb 2026

Org. Biomol. Chem., 2025, Accepted Manuscript

The Ugi-Joullié three-component (UJ-3CR) and related reactions. Recent developments, mechanistic aspects and synthesis of natural products and bioactive compounds

N. A. Lenarduzzi D'emilio, P. K. Paz Armero, A. R. Mendoza Salgado, T. S. Kaufman, S. O. Simonetti, A. B.J. Bracca and E. L. Larghi, Org. Biomol. Chem., 2025, Accepted Manuscript , DOI: 10.1039/D5OB02009C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements