Preparation of unsymmetrical biaryls via Ni- or Pd-catalyzed coupling of aryl chlorides with arylzincs
β Scribed by Joseph A. Miller; Robert P. Farrell
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 224 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Unsymmetrical biaryls may be prepared in an efficient manner using aryl chlorides as substrates in Negishi-type cross-coupling reactions with arylzinc reagents via either Ni-or Pd-catalysis.
Since a wide range of functional groups (e.g., nitrile, carbonyl, ester) tolerate arylzinc compounds, this methodology allows for the direct synthesis of biaryls from aryl chlorides possessing these moieties.
π SIMILAR VOLUMES
## Abstract A bimetallic catalyst system has been developed that for the first time allows the decarboxylative crossβcoupling of aryl and acyl carboxylates with aryl triflates. In contrast to aryl halides, these electrophiles give rise to nonβcoordinating anions as byproducts, which do not interfer