Sigmatropic tautomerism between n-allyl-3-isoxazolin-5-ones and 4-allyl-2-isoxazolin-5-ones
โ Scribed by Yosuo Makisumi; Takashi Sasatani
- Book ID
- 104239071
- Publisher
- Elsevier Science
- Year
- 1969
- Tongue
- French
- Weight
- 178 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
In continuation of our studies of 3,3-sigmatropic reactions, we have discovered the facile amino-Claisen rearrangement of the N-allyl-enamine system in pyrazolin-5-ones (1). Recent reports (2, 3,4) on the analogous examples of the amino-Claisen rearrangement prompt a preliminary report of our work on the sigmatropic tautomerism between N-allyl-3-isoxazolin-5-ones and 4-allyl-2-isoxazolin-5-ones.
๐ SIMILAR VOLUMES
The 3,5-isoxazolidinediones and 2-isoxazolin-5-ones demonstrated potent cytotoxicity against the growth of human Tmolt3 T cell leukemia, murine P388 and L1210 leukemias, as well as human HeLa-S3 uterine carcinoma and glioma tumor cell growth. The specificity of the 3,5-isoxazolidinedione and 2-isoxa