| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1327288 | Journal of Organometallic Chemistry | 2007 | 4 Pages |
Abstract
Suzuki cross-coupling reaction was successfully carried out in ethylene glycol under phosphine-free conditions to obtention of biaryls using ultrasonic irradiation. High yields were obtained using different palladium and bases sources. The catalyst was recycled up to three times with good to moderate activity.
Graphical abstractSuzuki cross-coupling reaction was carried out in ethylene glycol under phosphine-free condition to obtention of biaryls using ultrasonic irradiation. High yields were obtained using different palladium and bases sources. The catalyst was recycled up to three times with good to moderate activity.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Aires da Conceição Silva, Andréa Luzia F. de Souza, O.A.C. Antunes,