| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 64645 | Journal of Molecular Catalysis A: Chemical | 2016 | 5 Pages |
Abstract
•High catalytic activity of palladium supported on polysiloxane microspheres in Suzuki reaction.•High catalytic efficiency at low amount of Pd.•Good selectivity to different substituted benzophenones at low CO pressure.
Carbonylative Suzuki–Miyaura cross-coupling reactions of various aryl iodides with phenylboronic acids were catalyzed by palladium supported on amino-modified silica microspheres. Reactions performed with a very low concentration of Pd, under the atmospheric pressure of CO, led to high/moderate yields of multiple benzophenones.
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Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
Wojciech Zawartka, Piotr Pośpiech, Marek Cypryk, Anna M. Trzeciak,