Nitrierung des 6-Methyl-und 3-Bromchinolin-N-oxydes mit Benzoylnitrat.

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概要

• 論文の詳細を見る

• Die Nitrierung des 6-Methyl- bzw. 3-Bromchinolin-N-oxydes mit Benzoylnitrat verlauft prinzipiell ganz ahnlich wie beim Chinolin-N-oxyd. Es entsteht ein Mononitroderivat des entsprechenden Chinolin-N-oxydes und N-Benzoyloxycarbostyrils. Zu bemerken ist dabei, dass wegen der Blockierung der 3-bzw. 6-Stellung nur die Mononitrierung auf 6- bzw. 3-Stellung und keine weitere Nitrierung stattfindet.

• 公益社団法人日本薬学会の論文
• 1959-03-20

著者

• 金子 主税

  Faculty Of Pharmaceutical Sciences Kanazawa University

• 金子 主税

  Pharmaceutical Institute Medical Faculty University Of Tokyo

• 落合 英二

  Pharmazeutische Fakultat, Universitat Tokio

• 落合 英二

  ITSUU Laboratory

• 落合 英二

  Pharm. Institut D. Mediz. Fakultat D. Universitat Tokyo

• 落合 英二

  Faculty Of Pharmaceutical Sciences University Of Tokyo And Research Laboratory Shionogi & Co. Lt

• 金子 主税

  Pharmaceutical Institute Tohoku University

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