Studies on Tertiary Amine Oxides. IV. Some Reaction of N-(ρ-Dimethylaminophenyl)-α-(1-oxido-2-pyridyl) nitrone. (1)

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概要

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• The aldonitirone function of N-(p-dimethylaminophenyl)-α-(1-oxido-2-pyridyl) nitrone (I) was shown to undergo facile rearrangement with various reagents, such as sulfur dioxide, thionyl and sulfuryl chloride, phosphorus trichloride, phosphoryl chloride, triphenyl phosphate, and acetic anhydride. To elucidate some of these rearrangement, a cyclic mechanism was postulated.

• 公益社団法人日本薬学会の論文
• 1960-08-25

著者

• 梅沢 文輔

  Faculty of Pharmaceutical Sciences, Science University of Tokyo

• 梅澤 文輔

  Faculty Of Pharmaceutical Sciences Science University Of Tokyo

• 梅沢 文輔

  Faculty Of Pharmaceutical Sciences Science University Of Tokyo

• 梅沢 文輔

  Pharmaceutical Institute, Medical Faculty, University of Kyushu

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