| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5214684 | Tetrahedron | 2015 | 14 Pages |
Abstract
Site-selective arylation of commercially available 2,3,5,6-tetrachloropyridine has been accomplished, using the Suzuki–Miyaura reaction. The reaction conditions were thoroughly optimized, allowing the selective synthesis of mono-, di-, tri- and tetraarylated pyridines in good to quantitative yields. In addition, we studied the electrochemical properties of selected tetraarylpyridines by DPV-measurements.
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