Kinetics and mechanism of the palladium (II) promoted ring opening of tri- and tetrasubstituted cyclopropenes
β Scribed by Merle A. Battiste; Louis E. Friedrich; Bocco A. Fiato
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- French
- Weight
- 202 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
An example of an interesting and potentially general method for preparing pi-ally1 palladium chloride complexes from reaction of cyclopropeues with palladium (II) chloride was receutly reported. In the specific case cited2, 1,2,3-triphenylcyclopropene (&) was converted to di-~-chlorobis(n-l-chloro-syn,eyn-l,2,3-triphenylally~)pall~l~(II) In 80% isolated yield.
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