Abstract
Simple catalysts formed in situ from iron chloride and a wide range of monodentate and bidentate phosphines and arsines have been screened in the coupling of alkyl halides bearing -hydrogens with aryl Grignard reagents. The best of these show excellent activity, as do catalysts formed in situ with monodentate trialkyl and triaryl phosphite ligands. N-heterocyclic carbene-based precatalysts, either preformed or made in situ, also show excellent performance.
| Translated title of the contribution | Iron-phosphine, -phosphite, -arsine, and -carbene catalysts for the coupling of primary and secondary alkyl halides with aryl Grignard reagents |
|---|---|
| Original language | English |
| Pages (from-to) | 1104 - 1110 |
| Number of pages | 7 |
| Journal | Journal of Organic Chemistry |
| Volume | 71 (3) |
| DOIs | |
| Publication status | Published - Feb 2006 |
Bibliographical note
Publisher: American Chemical SocietyResearch Groups and Themes
- Inorganic & Materials