Heterocycles. XX. : Reactions of 2"-Methoxymethoxychalcone Epoxides under Acidic Conditions
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概要
- 論文の詳細を見る
The effect of substitutents on the formation of products in the reactions of 2"-methoxymethoxychalcone epoxides under acidic conditions has been examined. Regardless of the 6"-substitutent, the presence of a 4'-hydroxyl group results in the exclusive formation of flavanonols. The presence of a 4'-methoxyl group directs the reactions toward the competitive formation of flavanonols and glycol monomethyl ethers or toward the exclusive formation of glycol monomethyl ethers, depending on the bulk of the 6"-substituent.
- 社団法人日本薬学会の論文
- 1986-11-25
著者
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恩田 政行
School of Pharmaceutical Sciences, Kitasato University
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高橋 洋
School Of Pharmaceutical Sciences Kitasato University
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窪田 由美子
School Of Pharmaceutical Sciences Kitasato University
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恩田 政行
Shenyang Pharmaceutical University
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李 紹順
School of Pharmaceutical Sciences, Kitasato University
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林 方
School of Pharmaceutical Sciences, Kitasato University
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李 紹順
Shenyang Pharmaceutical University
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林 方
School Of Pharmaceutical Sciences Kitasato University
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