Beckmann Rearrangement of O-4-Pentenyl Oxime through N-Bromosuccinimide-Mediated Activating Process

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概要

• 論文の詳細を見る

• 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.

• 公益社団法人日本薬学会の論文
• 1997-01-15

著者

• Okada Midori

  Tokyo Women's Medical College

• TAGUCHI Takeo

  Tokyo University of Pharmacy and Life Science

• Kitagawa O

  Department Of Biology Tokyo Metropolitan University

• Kitagawa O

  Tokyo College Of Pharmacy

• Fujita M

  Discovery Research Laboratories Ii Dainippon Pharmaceutical Company Ltd.

• KITAGAWA Osamu

  Tokyo College of Pharmacy

• FUJITA Masao

  Tokyo College of Pharmacy

• Taguchi Takeo

  Tokyo College Of Pharmacy

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