Ecocatalyzed Suzuki cross coupling of heteroaryl compounds

被引:42
作者
Clave, Guillaume [1 ]
Pelissier, Franck [1 ]
Campidelli, Stephane [2 ]
Grison, Claude [1 ]
机构
[1] Univ Montpellier, CNRS, Bioinspired Chem & Ecol Innovat ChimEco, UMR 5021, 1682 Rue Valsiere, F-34790 Grabels, France
[2] Univ Paris Saclay, CEA Saclay, CNRS, LICSEN,NIMBE,CEA, F-91191 Gif Sur Yvette, France
关键词
WATER HYACINTH; EICHHORNIA-CRASSIPES; CATALYTIC-ACTIVITY; HETEROGENEOUS PALLADIUM; MEDIATED SYNTHESIS; MIYAURA REACTION; AQUEOUS-SOLUTION; LIGAND-FREE; GLYCEROL; NANOPARTICLES;
D O I
10.1039/c7gc01672g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:4093 / 4103
页数:11
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