Entstehung von 3-Hydroxyderivaten bei der N-Oxydierung der Chinolinderivate mittels Wasserstoffperoxyds in Eisessig-Losung.
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概要
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6-Nitrochinolin ergab bei der Oxydierung mit Wasserstoffperoxyd in einer Eisessig-Losung das entsprechende N-Oxyd nur in einer Ausbeute von 41% und nebenbei entstanden 3-Hydroxy-6-nitrochinolin und sein N-Oxyd in einer Ausbeute von 1% bzw. 27% der Theorie. Die analoge Reaktion mit chinolin-8-carbonsaure bzw. Seinem Athylester ergab kein N-Oxyd sondern das entsprechende 3-Hydroxyderivat in einer Ausbeute von 36% bzw. 21% der Theorie. Die Nebenentstehung von 3-Hydroxyderivat bei der N-Oxydierung eines Chinolinderivates mit Wasserstoffperoxyd in Eisessig-Losung scheint eine allgemeine Erscheinung zu sein, die bei der sterischen oder polarischen Hinderung durch irgendeinen Substituenten deutlicher auftritt.
- 社団法人日本薬学会の論文
- 1960-02-25
著者
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宮下 修一
Faculty Of Pharmaceutical Sciences University Of Kanazawa
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小菅 卓夫
Shizuoka College Of Pharmacy
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金子 主税
Faculty Of Pharmaceutical Sciences Kanazawa University
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金子 主税
Pharmaceutical Institute Medical Faculty University Of Tokyo
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落合 英二
Pharmazeutische Fakultat, Universitat Tokio
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島田 巌
Pharmazeutische Fakultat, Universitat Tokio
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村田 裕美子
Pharmazeutische Fakultat, Universitat Tokio
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小菅 卓夫
Pharmazeutische Fakultat, Universitat Kanazawa
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宮下 修一
Pharmazeutische Fakultat, Universitat Kanazawa
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川崎 遂志
Pharmazeutische Fakultat, Universitat Kanazawa
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落合 英二
ITSUU Laboratory
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宮下 修一
Pharmazeutische Fakultat Universitat Kanazawa
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落合 英二
Pharm. Institut D. Mediz. Fakultat D. Universitat Tokyo
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落合 英二
Faculty Of Pharmaceutical Sciences University Of Tokyo And Research Laboratory Shionogi & Co. Lt
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村田 裕美子
Pharmazeutische Fakultat Universitat Tokio
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小菅 卓夫
Pharmazeutische Fakultat Universitat Kanazawa
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小菅 卓夫
Pharmaceutical Faculty University Of Kanazawa.
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金子 主税
Pharmaceutical Institute Tohoku University
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川崎 遂志
Pharmazeutische Fakultat Universitat Kanazawa
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島田 巌
Pharmazeutische Fakultat Universitat Tokio
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