Synthesis of Methylpyridine Derivatives. XVI. The Reaction of Picolines and their N-Oxides with Amyl Nitrite.

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概要

• 論文の詳細を見る

• The reactions of picolines and their N-oxides with amyl nitrite in the presence of metal amide or sodium hydroxide in liquid ammonia afforded the corresponding aldoximes and acid amides in comparatively good yields. It may be concluded that the methyl group of picoline is much less reactive than that of N-oxide and that the reactivity of methyl group in the pyridine ring increases in the order of 3-, 2-, and 4-position.

• 公益社団法人日本薬学会の論文
• 1963-04-25

著者

• 加藤 鉄三

  Pharmaceutical Institute Tohoku University

• 後藤 良宣

  Faculty of Pharmaceutical Sciences, Fukuoka University

• 後藤 良宣

  Faculty Of Pharmaceutical Sciences Fukuoka University

• 後藤 良宣

  Pharmaceutical Institute, School of Medicine, Tohoku University

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