EQUILIBRIUM IN THE TRIETHYLAMINE-CATALYZED, EXTENDED BEHREND REARRANGEMENT OF N-(1-CYANOISOBUTYL) BENZYLIDENEAMINE N-OXIDES
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概要
- 論文の詳細を見る
Triethylamine-catalyzed Behrend rearrangement of the title aldonitrones to the corresponding keto-nitrones in various solvents is an entropy-controlled, energetically unfavorable reaction but the position of the equilibrium significantly depends on the nature of solvent used.
- 社団法人日本薬学会の論文
- 1985-03-25
著者
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日野 文男
明治薬科大学
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日野 文男
Meiji College of Pharmacy
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須田 晃治
Department of Physical Chemistry, Meiji College of Pharmacy
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関塚 悦子
Department of Physical Chemistry, Meiji College of Pharmacy
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若松 良子
Department of Physical Chemistry, Meiji College of Pharmacy
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日野 文男
Department of Physical Chemistry, Meiji College of Pharmacy
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飯島 千之
Department of Physical Chemistry, Meiji College of Pharmacy
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須田 晃治
明治薬科大学薬学部
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若松 良子
Department Of Physical Chemistry Meiji College Of Pharmacy
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飯島 千之
Department Of Physical Chemistry Meiji College Of Pharmacy
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関塚 悦子
Department Of Physical Chemistry Meiji College Of Pharmacy
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