## Abstract 1‐Methylallyl, 1,1‐dimethylallyl, 1,2‐dimethylallyl, 1,3‐dimethylallyl, 1,1,2‐trimethylallyl, and 1‐ethylallyl radicals have been generated in the gas phase at 20 ± 1°C by addition of H atoms, formed by Hg(6^3^__P__~1~) photosensitization of H~2~, to appropriate dienes. Their combinatio
Reaction of 2,6-di-t-butyl-4-propionylphenoxy radical with ethyl ferulate.
✍ Scribed by G. Brunow; T. Ilus
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- French
- Weight
- 90 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
The radical reactions of 2,6-di-t. butyl-1,4-benzoquinone with various thermally decomposing azocompounds and peroxides have been studied by ESR. On the basis of the ESR spectra of the intermediate radicals, the mechanism of the reaction is suggested. It was found that, while primary alkyl radicals
## 2,4-Di-t-butyl-6-methylphenylphosphonous dichloride reacted with chloroform in the presence of lithium diisopropylamide to give (2,4-di-t-butyl-6-methylphenyl) (dichloromethyl) ( I , 2,2-trichloroethenyl)phosphine. The structure of this phosphine was analyzed by X-ray crystallography. This phosph