Jump to main content
Jump to site search

Issue 17, 2017
Previous Article Next Article

Ecocatalyzed Suzuki cross coupling of heteroaryl compounds

Author affiliations

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.

Graphical abstract: Ecocatalyzed Suzuki cross coupling of heteroaryl compounds

Back to tab navigation

Supplementary files

Article information


Submitted
07 Jun 2017
Accepted
10 Jul 2017
First published
10 Jul 2017

Green Chem., 2017,19, 4093-4103
Article type
Paper

Ecocatalyzed Suzuki cross coupling of heteroaryl compounds

G. Clavé, F. Pelissier, S. Campidelli and C. Grison, Green Chem., 2017, 19, 4093
DOI: 10.1039/C7GC01672G

Social activity

Search articles by author

Spotlight

Advertisements