Stereochemistry of the Intramolecular Cyclization Products of Methyl 2-Bromo-5-(4-hydroxyphenyl) hexanoate : Synthesis of trans- and cis-1,4-Dimethyltetralin
スポンサーリンク
概要
- 論文の詳細を見る
The stereochemistry of the spirodienones (2) obtained by the intramolecular cyclization of methyl 2-bromo-5-(4-hydroxyphenyl) hexanoate (1) was established by carbon-13 nuclear magnetic resonance spectral analysis and chemical transformation to trans- and cis-1,4-dimethyltetralins (6).
- 公益社団法人日本薬学会の論文
- 1984-02-25
著者
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田中 徹明
Faculty of Pharmaceutical Sciences, Osaka University
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岩田 宙造
Faculty of Pharmaceutical Sciences, Osaka University
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前崎 直容
Faculty of Pharmaceutical Sciences, Osaka University
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前崎 直容
阪大院薬
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田中 徹明
阪大院薬
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田中 徹明
Faculty Of Pharmaceutical Sciences Osaka University
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Tanaka T
Osaka Univ. Osaka Jpn
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岩田 宙造
Faculty Of Pharmaceutical Sciences Osaka University
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符阪 隆文
Faculty of Pharmaceutical Sciences, Osaka University
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符阪 隆文
Faculty Of Pharmaceutical Sciences Osaka University
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