Studies on Tertiary Amine Oxides. XIII. Reactions of N-(p-Dimethylaminophenyl) nitrones having Pyridine N-Oxide, Quinoline or its N-Oxide as α-Substituent.

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概要

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• Reactions of N-dimethylaminophenylnitrones, having either pyridine or quinoline ring, as α-substituent, with six sorts of reagent such as SO_2,P(OPh)_3,PO(OPh)_3,were examined. The observation that the deoxygenation and the rearrangement reaction of these nitrones were competitive each other confirmed the conclusion that -I effect of the heteroaromatic ring was responsible for deoxygenation and that +M effect of Noxide group might cause rearrangement.

• 公益社団法人日本薬学会の論文
• 1962-10-25

著者

• 梅沢 文輔

  Faculty of Pharmaceutical Sciences, Science University of Tokyo

• 浜名 政和

  Faculty of Pharmaceutical Sciences, Kyushu University

• 梅澤 文輔

  Faculty Of Pharmaceutical Sciences Science University Of Tokyo

• 浜名 政和

  Institute of Pharmaceutical Sciences, Faculty of Medicine, Kyushu University

• 梅沢 文輔

  Faculty Of Pharmaceutical Sciences Science University Of Tokyo

• 浜名 政和

  Faculty Of Pharmaceutical Sciences Kyushu University

• 梅沢 文輔

  Institute of Pharmaceutical Sciences, Faculty of Medicine, Kyushu University

• 中島 松一

  Institute of Pharmaceutical Sciences, Faculty of Medicine, Kyushu University

• 中島 松一

  Institute Of Pharmaceutical Sciences Faculty Of Medicine Kyushu University

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