Reductive Radical Formation of Hetero Aromatic N-Oxides

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概要

• 論文の詳細を見る

• Pyridine 1-oxide gave the 4,4'-dipyridyl anion radical in 1,2-dimethoxyethane by reduction with the potassium metal in vacuo. The 3,5-lutidine, pyrazine and 3-nitropyridine anion radicals were also obtained from the parent N-oxides by the reduction, accompanied with the removal of oxygen atoms, while the 4-nitro- and 4-nitroso-pyridine 1-oxide anion radicals were obtained from the parent compounds without the deoxygenation.

• 公益社団法人日本薬学会の論文
• 1967-04-25

著者

• 岡本 敏彦

  Faculty Of Pharmaceutical Sciences University Of Tokyo

• 岡本 敏彦

  Sato Pharmaceutical Co. Ltd.

• 伊藤 道也

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 伊藤 道也

  Faculty Of Pharmaceutical Sciences The University Of Tokyo

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