Abstract
Beckmann rearrangement of O-4-pentenyl oxime derivatives proceeds in good yield under mild conditions through the formation of a cationic tetrahydrofuranium intermediate in the halocyclization reaction with N- bromosuccinimide.
| Original language | English |
|---|---|
| Pages (from-to) | 32-35 |
| Number of pages | 4 |
| Journal | Chemical and Pharmaceutical Bulletin |
| Volume | 45 |
| Issue number | 1 |
| Publication status | Published - 1997 Jan |
| Externally published | Yes |
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Keywords
- Beckmann rearrangement
- halocyclization
- N- bromosuccinimide
- O-4-pentenyl oxime
- tetrahydrofuranium
ASJC Scopus subject areas
- Chemistry(all)
- Organic Chemistry
- Drug Discovery
- Pharmacology
Cite this
Kitagawa, O., Fujita, M., Okada, M., & Taguchi, T. (1997). Beckmann rearrangement of O-4-pentenyl oxime through N- bromosuccinimide-mediated activating process. Chemical and Pharmaceutical Bulletin, 45(1), 32-35.