Abstract
The Suzuki-Miyaura reaction of 1,2-dibromo-3,5-difluorobenzene with two equivalents of arylboronic acids gave difluorinated ortho-terphenyls. The reaction with one equivalent of arylboronic acid resulted in site-selective formation of 2-bromo-3,5-difluoro-biphenyls. The one-pot reaction of 1,2-dibromo-3,5-difluorobenzene with two different arylboronic acids afforded difluorinated ortho-terphenyls containing two different terminal aryl groups.
| Original language | English |
|---|---|
| Pages (from-to) | 913-916 |
| Number of pages | 4 |
| Journal | Synlett |
| Issue number | 6 |
| DOIs | |
| State | Published - 2010 |
| Externally published | Yes |
Keywords
- Catalysis
- Organofluorine compounds
- Palladium
- Site selectivity
- Suzuki-Miyaura reaction
ASJC Scopus subject areas
- Organic Chemistry