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 |
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Pages (from-to) | 32-35 |
Number of pages | 4 |
Journal | Chemical and Pharmaceutical Bulletin |
Volume | 45 |
Issue number | 1 |
DOIs | |
Publication status | Published - 1997 Jan |
Externally published | Yes |
Keywords
- Beckmann rearrangement
- N- bromosuccinimide
- O-4-pentenyl oxime
- halocyclization
- tetrahydrofuranium
ASJC Scopus subject areas
- Chemistry(all)
- Drug Discovery