## Abstract The title compound **1b** was prepared by tritiolysis of 5‐(O‐bromophenyl)‐2‐dimethylamino‐2‐oxazolin‐4‐one, **2**, with 10 Ci of tritium and diluted with unlabelled **1a**. The mass spectrum of the 2′ ‐deutero derivative **1c**, prepared similarly, showed that 92.9 % of labelled compou
✦ LIBER ✦
Thermolysis of oxazolin-5-ones, 12. Formation of a cage compound by thermolysis of 2-(4-Chlorophenyl)-2-(3,3-dimethylallyl)-4-phenyl-5(2H)-oxazolone
✍ Scribed by Fischer, János ;Márványos, Ede ;Párkányi, László ;Kálmán, Alajos ;Steglich, Wolfgang
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1988
- Tongue
- English
- Weight
- 180 KB
- Volume
- 121
- Category
- Article
- ISSN
- 0009-2940
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✦ Synopsis
During thermolysis of title compound 1, the unusual cage compound 4 is formed (along with 2,3dihydropyridine 3); the structure of 4 was determined by X-ray structure analysis. The formation of 4 can be explained by dimerization of the intermediates 2 and 3.
Thermol ysis of 2-(4-chlorophenyl)-2-(3,3-dimethylallyl)-4-phenyl-
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