Ecocatalyzed Suzuki cross coupling of heteroaryl compounds

Abstract : A bio-based EcoPd was developed for the Suzuki cross coupling of heteroaryl compounds. Based on the ability of Eichhornia crassipes to bioconcentrate Pd in its roots, we addressed the transformation of plant-derived Pd metals to green catalysts. The methodology is based on eco-friendly procedures. It allowed the preparation of a wide range of heterocyclic biaryl and heterocyclic–heterocyclic biaryl compounds, with a low Pd catalyst loading. EcoPd was found to have the ideal microstructure to promote complex Suzuki reactions without ligands or additives. For the first time, post-reaction solution was treated by rhizofiltration. The resulting EcoPd has been reused with the same performance. This work has established the ecocatalysis concept as a powerful strategy for Pd sustainability, with the development of homogeneous catalysts that are easily recycled and reused.
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Green Chemistry, Royal Society of Chemistry, 2017, 19, pp.4093-4103. 〈http://dx.doi.org/10.1039/C7GC01672G〉. 〈10.1039/c7gc01672g〉
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https://hal-cea.archives-ouvertes.fr/cea-01577263
Contributeur : Serge Palacin <>
Soumis le : vendredi 25 août 2017 - 11:27:54
Dernière modification le : jeudi 15 mars 2018 - 15:06:18

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Guillaume Clavé, Franck Pelissier, Stéphane Campidelli, Claude Grison. Ecocatalyzed Suzuki cross coupling of heteroaryl compounds. Green Chemistry, Royal Society of Chemistry, 2017, 19, pp.4093-4103. 〈http://dx.doi.org/10.1039/C7GC01672G〉. 〈10.1039/c7gc01672g〉. 〈cea-01577263〉

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