Preparation and Ring Conversion of Furo [2,3-b] quinoxaline
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概要
- 論文の詳細を見る
The reaction of 3-ethoxycarbonylmethylene-2-oxo-1,2,3,4-tetrahydroquinoxaline with the Vilsmeier reagent gave 3-(N, N-dimethylaminocarbonyl) furo [2,3-b] quinoxaline, which was converted to various quinoxaline derivatives, 3-methyl-2-oxo-1,2-dihydroquinoxaline, quinoxalinylpyrazolin-5-ones, and pyrazolo [3', 4' : 3,4] pyridazino [5,6-b] quinoxalines.
- 社団法人日本薬学会の論文
- 1981-10-25
著者
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高田 純
北里大(薬)
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高田 純
School of Pharmaceutical Sciences, Kitasato University
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倉澤 嘉久
School of Pharmaceutical Sciences, Kitasato University
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高田 純
School Of Pharmaceutical Science Kitasato University
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倉澤 嘉久
School Of Pharmaceutical Sciences Kitasato University
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