Beckmann rearrangement of O-4-pentenyl oxime through N- bromosuccinimide-mediated activating process

Osamu Kitagawa, Masao Fujita, Midori Okada, Takeo Taguchi

Research output: Contribution to journalArticle

9 Citations (Scopus)

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 languageEnglish
Pages (from-to)32-35
Number of pages4
JournalChemical and Pharmaceutical Bulletin
Volume45
Issue number1
Publication statusPublished - 1997 Jan
Externally publishedYes

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Bromosuccinimide
Oximes
Derivatives

Keywords

  • Beckmann rearrangement
  • halocyclization
  • N- bromosuccinimide
  • O-4-pentenyl oxime
  • tetrahydrofuranium

ASJC Scopus subject areas

  • Chemistry(all)
  • Organic Chemistry
  • Drug Discovery
  • Pharmacology

Cite this

Beckmann rearrangement of O-4-pentenyl oxime through N- bromosuccinimide-mediated activating process. / Kitagawa, Osamu; Fujita, Masao; Okada, Midori; Taguchi, Takeo.

In: Chemical and Pharmaceutical Bulletin, Vol. 45, No. 1, 01.1997, p. 32-35.

Research output: Contribution to journalArticle

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