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Inhibition of Homo-coupling of Arylboronic Acids in Ligand Free Pd(II)-Catalyzed Suzuki Reaction
✍ Scribed by Xiao-Chun Tao; Yue-Ping Zhang; Tian-Xiong He; Dong Shen
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 57 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0256-7660
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✦ Synopsis
Abstract
A series of solvents were examined for the ligand free Pd(II)‐catalyzed Suzuki reaction of 4‐bromotoluene with phenylboronic acid. It was found that the PdCl~2~/i‐PrOH system could efficiently inhibit the homo‐coupling of phenylboronic acid and give a cross‐coupling product in high yields. The substrates with a wide variety of functional groups were tolerated in the system. A possible mechanism for this system was proposed.
📜 SIMILAR VOLUMES
## Abstract The boron trifluoride induced Suzuki‐Miyaura cross‐coupling of aryltriazenes with arylboronic acids catalyzed by Pd(OAc)~2~ without added ligands has been achieved for the first time. The reactions performed at room temperature under an argon atmosphere give biaryls in good to excellent