Site‐Selective Synthetic Modifications of the Cinchona Alkaloids

Abstract The natural product quinine has been known to humankind for centuries, and in that time has played a pivotal role in the treatment of malaria. Quinine, and the related cinchona alkaloids, have seen widespread contemporary use across chemical and biological disciplines, owing in part to the plethora of functional groups and stereochemical information contained within their scaffold. This review focuses on site‐selective synthetic modifications of the cinchona alkaloids. Our comparative analysis may act as a ‘user manual’ for the selective functionalisation of the cinchona alkaloids, and aims to promote consideration of remarkable and lesser‐understood aspects of cinchona chemistry.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2024-10-07
DOI
https://doi.org/10.1002/ajoc.202400397
Citations
3
Primary Topic
Chemical synthesis and alkaloids
Type
article
Field-Weighted Citation Impact
0.75

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article

Site‐Selective Synthetic Modifications of the Cinchona Alkaloids

Daniel J. Foley, Finlay P. Player
3 citations
Asian Journal of Organic Chemistry
Chemical synthesis and alkaloids
0.75
article

Site‐Selective Synthetic Modifications of the Cinchona Alkaloids

Daniel J. Foley, Finlay P. Player
article en
3 citations

Abstract

Abstract The natural product quinine has been known to humankind for centuries, and in that time has played a pivotal role in the treatment of malaria. Quinine, and the related cinchona alkaloids, have seen widespread contemporary use across chemical and biological disciplines, owing in part to the plethora of functional groups and stereochemical information contained within their scaffold. This review focuses on site‐selective synthetic modifications of the cinchona alkaloids. Our comparative analysis may act as a ‘user manual’ for the selective functionalisation of the cinchona alkaloids, and aims to promote consideration of remarkable and lesser‐understood aspects of cinchona chemistry.

Asian Journal of Organic ChemistryVol. 13(12)
University of Canterbury (NZ)
Royal Society of Chemistry
Openalex Percentile: Top 32%
Chemical synthesis and alkaloids
0.75
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