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On the catalytic cycle of the palladium-catalyzed cross-coupling reaction of alkynylstannane with aryl iodide

✍ Scribed by Eiji Shirakawa; Hiroto Yoshida; Tamejiro Hiyama


Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
218 KB
Volume
38
Category
Article
ISSN
0040-4039

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✦ Synopsis


The coupling reaction of phenylcthynyltributyltin with (4-trifluoromethyl)iodobenzene catalyzed by a Pd(0) complex coordinated by N-(2-diphenylphosphinobenzylidene)-2-phenylethylamine was found to start with oxidative addition of the tin reagent to the Pd(0) complex. In contrast, the use of 1,3-bis(diphenylphosphino)propane as the ligand switched the catalytic cycle to the well-accepted one initiated by oxidative addition of the aryl iodide to the Pd(0) complex.


πŸ“œ SIMILAR VOLUMES


Palladium-catalyzed cross-coupling react
✍ Alexey V Tsvetkov; Gennadij V Latyshev; Nikolai V Lukashev; Irina P Beletskaya πŸ“‚ Article πŸ“… 2000 πŸ› Elsevier Science 🌐 French βš– 217 KB

Cross-coupling reactions of bis(ferrocenyl)mercury with aryl-and heteroaryl iodides were shown to be easy and convenient for the synthesis of monoarylsubstituted ferrocenes in high yields. The highly selective substitution of iodine atom in iodobromoarenes by the ferrocenyl unit was demonstrated.

ChemInform Abstract: Palladium-Catalyzed
✍ Alexey V. Tsvetkov; Gennadij V. Latyshev; Nikolai V. Lukashev; Irina P. Beletska πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 30 KB πŸ‘ 1 views

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