On the catalytic cycle of the palladium-catalyzed cross-coupling reaction of alkynylstannane with aryl iodide
β 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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β¦ 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.
π SIMILAR VOLUMES
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.
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