Studies on Tetralin Derivatives. XI. Synthesis of 5-Hydroxy-6-acyl-1,4-naphthoquinones
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概要
- 論文の詳細を見る
The Fries rearrangement of 5,8-dimethoxy-1-naphthol acylate gave 2-acyl-5,8-dimethoxy-1-naphthol in a yield of 24〜56%. These acyl compounds were demethylated and oxidized to 5-hydroxy-6-acyl-1,4-napthoquinones.
- 公益社団法人日本薬学会の論文
- 1959-12-20
著者
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合屋 周次郎
Pharmaceutical Institute Medical Faculty University Of Kyushu
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百瀬 勉
Meiji College Of Pharmacy
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百瀬 勉
Pharmaceutical Institute Medical Faculty University Of Kyushu
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