^<13>C Nuclear Magnetic Resonance Spectra of Hydrolyzable Tannins. II. : Tannins Forming Anomer Mixtures
スポンサーリンク
概要
- 論文の詳細を見る
The glucose carbon signals in the ^<13>C nuclear magnetic resonance (NMR) spectra of hydrolyzable tannins forming anomer mixtures, which differ from each other in the locations of acyl groups, were assigned. The utility of these data was demonstrated by application to the structural assignments of recently isolated dimeric hydrolyzable tannins [e.g., camptothin A (13) and camptothin B (14)].
- 1988-08-25
著者
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吉田 隆志
Department Of Pharmacognosy College Of Pharmaceutical Sciences Matsuyama University
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波多野 力
Faculty of Pharmaceutical Sciences, Okayama University
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Hatano Tsutomu
エジプト
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奥村 智子
Faculty Of Pharmaceutical Sciences Okayama University
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新宮 徹朗
Faculty Of Pharmaceutical Sciences Kobe Gakuin University
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新宮 徹朗
神戸学院大学薬学部薬化学講座
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Shingu K
Kumamoto Univ. Kumamoto Jpn
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新宮 徹朗
神院大・薬
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新宮 徹朗
京都大学薬学部
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奥田 拓男
Faculty Of Parmaceutical Sciences University
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Shingu K
School Of Pharmacy Kobe Gakuin University
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吉田 隆志
Faculty Of Pharmaceutical Sciences Kyoto University
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