THE ABSOLUTE CONFIGURATION AND CONFORMATION OF NEOCURDIONE
スポンサーリンク
概要
- 論文の詳細を見る
The complete stereostructure of neocurdione (1a) from Curcuma wenyujin and C. aromatica was determined unequivocally on the basis of chemical transformation of curdione (2a) to 4-epicurdione (1b) as well as X-ray crystallography of the p__-bromobenzoate (3b) of 8αH-dihydro-4-epicurdione (3a). The preferred conformation of 1__〜a in solution was found to be A [C(10)-CH_3/C(5)=O : anti] based on ^1H-NMR spectromethy at various temperatures, and NOE measurements, especially at -60℃. In contrast, the preferred conformation of 1__〜a in crystals (X-ray) was found to be B__〜 [C(10)-CH_3/C(5)=O : syn]. A conformational analysis of 1__〜a, 1__〜b and 2__〜a is also presented based on molecular dynamics calculations using MM2.
- 公益社団法人日本薬学会の論文
- 1986-10-25
著者
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大倉 多美子
Pharmaceutical Institute School Of Medicine Keio University
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飯高 洋一
Nishi-tokyo Science University
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飯高 洋一
Faculty of Pharmaceutical Sciences, The University of Tokyo
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福島 清吾
Shizuoka College of Pharmacy
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黒柳 正典
Shizuoka College of Pharmacy
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稲山 誠一
Pharmaceutical Institute, School of Medicine, Keio University
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飯高 洋一
School Of Medicine Teikyo University
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飯高 洋一
Faculty Of Pharmaceutical Sciences University Of Tokyo
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飯高 洋一
西東京科学大学理工学部
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播磨谷 健蔵
Pharmaceutical Institute, Tohoku University
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引地 学
Pharmaceutical Institute, School of Medicine, Keio University
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川又 健
Pharmaceutical Institute, School of Medicine, Keio University
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黒柳 正典
School Of Pharmaceutical Sciences University Of Shizuoka
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高 集馥
Pharmaceutical Institute, School of Medicine, Keio University
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高 集馥
Pharmaceutical Institute School Of Medicine Keio University
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稲山 誠一
Institute Of Oriental Medical Sciences
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稲山 誠一
Pharmaceutical Institute School Of Medicine Keio University
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稲山 誠一
慶應義塾大学医学部薬化学研究所
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播磨谷 健蔵
Pharmaceutical Institute School Of Medicine Keio University
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川又 健
Pharmaceutical Institute School Of Medicine Keio University
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飯高 洋一
Faculty Of Pharmaceutical Sciences The University Of Tokyo
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引地 学
Pharmaceutical Institute School Of Medicine Keio University
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