Homogeneous isoaromatization of alicyclic dienones catalyzed by complexes of the platinum group
β Scribed by Yechiel Pickholtz; Yoel Sasson; Jochanan Blum
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- French
- Weight
- 156 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The isoaromatization of alicyclic dienones by heterogeneous catalysts (e.g., Ni, Pd-C, PtOl ' ), provides a rather useful method for the synthesis of monocyclic phenols. Polycyclic ketones, however, are often deoxygenated to give hydroxyl-free hydrocarbons*.
We wish to report the isoaromatization of alicyclic ketones by homogeneous Flu, Rh and Ir catalysts,
π SIMILAR VOLUMES
Benedict for performing the X-ray structural determinations and Prof. K. McNeill (University of Minnesota) for initial samples of the ligand 3.
A variety of Group VIII transition metal phosphine complexes were shown to be active catalysts for hydrogenation of nitroaliphatic compounds. The catalysis was determined to be homogeneous based on results of selective catalyst poisoning experiments using dibenzo[a,e]cyclooctatetraene and Hg. A deut
## Numerous examples have been reported1 wherein acids, bases or salts catalyzed the rearrangement of substituted ethylene oxides. However, only a few cases are known in which transition metal complexes promote the homogeneous transformation of internal epoxides to ketones. Cobalt and iron