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Recent developments in the total synthesis of natural products using the Ugi multicomponent reactions as the key strategy

Enrique L. Larghi, Andrea B. J. Bracca, Sebastián O. Simonetti, Teodoro S. Kaufman

2023Organic & Biomolecular Chemistry19 citationsDOI

Abstract

The total syntheses of selected natural products using different versions of the Ugi multicomponent reaction is reviewed on a case-by-case basis. The revision covers the period 2008-2023 and includes detailed descriptions of the synthetic sequences, the use of state-of-the-art chemical reagents and strategies, as well as the advantages and limitations of the transformation and some remedial solutions. Relevant data on the isolation and bioactivity of the different natural targets are also briefly provided. The examples clearly evidence the strategic importance of this transformation and its key role in the modern natural products synthetic chemistry toolbox. This methodology proved to be a valuable means for easily building molecular complexity and efficiently delivering step-economic syntheses even of intricate structures, with a promising future.

Topics & Concepts

ToolboxComputer scienceBiochemical engineeringUgi reactionKey (lock)Total synthesisNatural (archaeology)Combinatorial chemistryChemistryOrganic chemistryEngineeringIsocyanideProgramming languageGeographyArchaeologyComputer securityMulticomponent Synthesis of HeterocyclesChemical Synthesis and AnalysisMicrobial Natural Products and Biosynthesis