Abstract
A new chemical method is described for the preparation of aryl or thienyl zinc intermediates from their corresponding aromatic or thienyl chlorides in a mixture of acetonitrile-pyridine, using cobalt catalysis. This procedure allows for the synthesis of a variety of functionalized arylzinc species from reactive arylchlorides or chlorothiophenes in good to excellent yields. Some of these arylzinc compounds have been coupled with aromatic bromides using palladium catalysis.
| Original language | English |
|---|---|
| Pages (from-to) | 2171-2174 |
| Number of pages | 4 |
| Journal | Synlett |
| Issue number | 14 |
| DOIs | |
| Publication status | Published - 2 Sept 2005 |
Keywords
- Aromatic chlorides
- Catalysis
- Cobalt halide
- Thiophenes
- Zinc