The prototropic rearrangement of 3-phenyl-1 -propenes to the corresponding l-phenyl-I-propenes was investigated in basic media utilizing 0.1M sodium ethoxide in absolute ethanol at 81Β°C. I t was found that the effect of substituents on the rate of such isomerizations follows the order: p -N 0 2 > a-
β¦ LIBER β¦
Base-catalyzed equilibrium isomerization of the methylcyclopentenes
β Scribed by Joseph Shabtai; Emanuel Gil-Av
- Publisher
- Elsevier Science
- Year
- 1964
- Tongue
- French
- Weight
- 194 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0040-4039
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