Abstract
Herein, a cobalt-catalysed Negishi-type cross-coupling of amide derivatives is described. Apart from being the first example of cobalt-catalysed Negishi-type coupling of amides, the process described employs a unique, simple, and cheap catalytic system to perform both the organozinc formation and the Negishi-type coupling. Indeed, the same cobalt(II) bromide salt used to form the arylzinc species from aryl bromides is then re-used to perform the cross coupling of this resulting arylzinc with N-benzoyl glutarimides at room temperature. The main advantages of the reaction presented are its robustness and ease of use. Indeed, the reactions of organozinc formation and Negishi-type coupling are performed without precautions toward water or oxygen. (Figure presented.).
| Original language | English |
|---|---|
| Pages (from-to) | 1777-1780 |
| Number of pages | 4 |
| Journal | Advanced Synthesis and Catalysis |
| Volume | 361 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 16 Apr 2019 |
| Externally published | Yes |
Keywords
- Amides
- Cobalt
- Negishi-type cross-coupling
- One-pot reaction
- Organozinc reagent
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