𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Preparation of unsymmetrical biaryls via Ni- or Pd-catalyzed coupling of aryl chlorides with arylzincs

✍ 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

No coin nor oath required. For personal study only.

✦ 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.


πŸ“œ SIMILAR VOLUMES


Biaryl and Aryl Ketone Synthesis via Pd-
✍ Lukasβ€…J. Goossen; Christophe Linder; Nuria RodrΓ­guez; Paulβ€…P. Lange πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 853 KB

## Abstract A bimetallic catalyst system has been developed that for the first time allows the decarboxylative cross‐coupling of aryl and acyl carboxylates with aryl triflates. In contrast to aryl halides, these electrophiles give rise to non‐coordinating anions as byproducts, which do not interfer