Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5222092 | Tetrahedron | 2011 | 5 Pages |
Abstract
An ultrafast and highly efficient ligand-free Suzuki-Miyaura cross-coupling reaction between aryl bromides/iodides and arylboronic acids using palladium chloride as catalyst in PEG400/H2O in air at room temperature has been developed. TEM showed that palladium nanoparticles were generated in situ from PdCl2/PEG400/H2O without use of other reductants. The catalyst system can be recycled to reuse three times with good yields.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Zhengyin Du, Wanwei Zhou, Fen Wang, Jin-Xian Wang,