Synthesis of a New Bichalcone via Suzuki–Miyaura Coupling Reaction
Unlike the wide number of natural biflavonoids, natural bichalcones are a rare and even less studied class. Nevertheless, some of them have proved their interest in the fight against cancer through their cytotoxic activity against human tumor cell lines. The aim of this study was to synthesize a novel bichalcone: 3′,3‴,4,4′,4″,4‴,5′,5‴-octamethoxy-2,3″-bichalcone 1. The most efficient synthetic pathway was the Suzuki–Miyaura reaction between a boronated chalcone and a brominated one.
Authors
- Catherine Fagnère
- Yves Champavier (ORCID: https://orcid.org/0000-0003-4131-7787)
- Christelle Pouget (ORCID: https://orcid.org/0000-0001-6067-8575)
- François‐Xavier Toublet (ORCID: https://orcid.org/0000-0001-5630-6920)
- Aurélie Lévêque
Institutions
- Centre National de la Recherche Scientifique (FR)
- Inserm (FR)
- Université de Limoges (FR)
Publication Details
- Journal
- Molbank
- Published
- 2025-05-25
- DOI
- https://doi.org/10.3390/m2012
- Primary Topic
- Synthesis of Organic Compounds
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Centre National de la Recherche Scientifique
- Université d'Orléans