Influence of Substituent Groups on Nuclear Reactivity in Formations of Substituted Biphenyls through Reactions of Aromatic Diazo and Cognate Compounds with Aromatic Liquids. I. The Nitro Group
スポンサーリンク
概要
- 論文の詳細を見る
The reactions of both <I>n</I>-nitrosoacetanilide and diazobenzene hydroxide with nitrobenzene give all three isomeric nitrobiphenyls, whereas the formation of only the ortho and para isomerides has been reported in the literature. All the nuclear positions of nitrobenzene are more reactive than that of benzene towards the substituting phenyl radical.
- 社団法人 日本化学会の論文
著者
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Inukai Takashi
Department of Chemistry Faculty of Science The University of Tokyo
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Simamura Osamu
Department of Chemistry Faculty of Science The University of Tokyo
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Inukai Takashi
Department of Chemistry, Faculty of Science, The University of Tokyo
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Simamura Osamu
Department of Chemistry, Faculty of Science, The University of Tokyo
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Kanazashi Motonori
Department of Chemistry, Faculty of Science, The University of Tokyo
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