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

Osamu Kitagawa, Masao Fujita, Midori Okada, Takeo Taguchi

研究成果: Article

9 引用 (Scopus)

抄録

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.

元の言語English
ページ(範囲)32-35
ページ数4
ジャーナルChemical and Pharmaceutical Bulletin
45
発行部数1
出版物ステータスPublished - 1997 1
外部発表Yes

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Bromosuccinimide
Oximes
Derivatives

ASJC Scopus subject areas

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

これを引用

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

:: Chemical and Pharmaceutical Bulletin, 巻 45, 番号 1, 01.1997, p. 32-35.

研究成果: Article

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KW - N- bromosuccinimide

KW - O-4-pentenyl oxime

KW - tetrahydrofuranium

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