Studies on the Heterocyclic Compounds. XIX. A Novel Ring Isomerization of 3-Ylideneaminoimidazo [4,5-c] pyridazines
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概要
- 論文の詳細を見る
Several 3-ylideneaminoimidazo [4,5-c] pyridazines (IV and VI) were synthesized for the investigation of the ring isomerization reaction. The reactions of IVa, IVb, IVc, and IVd with 5% or 50% acetic acid gave VIII as the ring isomerization product. Similarly IVe afforded X. In the case of IVd, intermediate product (IXd) was obtained by the reaction with 50% acetic acid. This compound (IXd) was converted to VIII by the treatment with 70% acetic acid. The possible reaction mechanism was proposed.
- 公益社団法人日本薬学会の論文
- 1975-08-25
著者
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木下 敏夫
Faculty of Pharmaceutical Sciences, Nagasaki University
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梁井 光二
Faculty Of Pharmaceutical Sciences Nagasaki University
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武田 成子
Faculty of Pharmaceutical Sciences, Nagasaki University
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木下 敏夫
School of Pharmaceutical Sciences, Nagasaki University
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西村 正邦
Faculty of Pharmaceutical Sciences, Nagasaki University
-
武田 成子
Faculty Of Pharmaceutical Sciences Nagasaki University
-
木下 敏夫
School Of Pharmaceutical Sciences Nagasaki University
-
西村 正邦
Faculty Of Pharmaceutical Sciences Nagasaki University
-
梁井 光二
Faculty of Pharmaceutical Sciences, Nagasaki University
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