Studies on Oxytetracycline and Related Compounds. XI. Synthesis of Terranaphthol.
スポンサーリンク
概要
- 論文の詳細を見る
The structure of terranaphthol, a degradation product of oxytetracycline, was identified as 4,5-dihydroxy-2-hydroxymethyl-1-methylnaphthalene (Ib) by its synthesis through the Hauser rearrangement of 4,5-dimethoxy-1-dimethylaminomethylnaphthalene methiodide (VIIb).
- 公益社団法人日本薬学会の論文
- 1959-06-10
著者
-
堀井 善一
Pharmaceutical Faculty University Of Osaka
-
二宮 一彌
Medicinal Chemistry Laboratory Kobe Women's College Of Pharmacy
-
田村 恭光
Pharmaceutical Faculty, University of Osaka
-
二宮 一彌
Pharmaceutical Faculty, University of Osaka
関連論文
- Itaconic Acid in Organic Chemistry. I. Synthesis of 2-Methyl-1,4-naphthoquinone (Menadione).
- Leuckart反応の一変法(第2報)
- Synthesis of 4-Carboxymethylthio-Substituted Steroids for Enzyme Immunoassay
- A Modified Leuckart Reaction. III. Rearrangement in the Leuckart Reaction.
- Studies on Oxytetracycline and Related Compounds. XI. Synthesis of Terranaphthol.
- Studies on Terramycin and Related Compounds. IX. Synthesis of 3-(o-Carboxy-phenyl) butyric Acid via the Reformatsky Reaction.
- Studies on Oxytetracycline and Related Compounds. X. Synthesis of Terranaphthoic Acid.
- Synthesis of 1,8-Dihydroxy-4-methyl-3-naphthoic Acid : Terranaphthoic Acid