Synthesis of Methoxyonychine and Use of ^1H- and ^<13>C-Nuclear Magnetic Resonance Spectra for Structure Determination of Geometrical Isomers of Indan-1-one Oxime Derivatives
スポンサーリンク
概要
- 論文の詳細を見る
Synthesis of an alkaloid, methoxyonychine, was accomplished by an application of a synthetic method for constructing cycloalkenopyridines from oxime O-allyl ethers, and its structure was confirmed. During the course of the synthesis, the chemical shift differences of the signals of C_7-H and C_1,C_7,and C_<7a> in the ^1H- and ^<13>C-nuclear magnetic resonanace spectra were employed for the stereostructure determination of E- and Z-isomers of oxime O-methyl and O-allyl ethers of indan-1-ones.
- 社団法人日本薬学会の論文
- 1988-08-25
著者
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多賀 徹
Faculty of Pharmaceutical Sciences, Kyoto University
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町田 勝之輔
Faculty of Pharmaceutical Sciences, Kyoto University
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入江 寛
長崎大薬
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入江 寛
長崎大学薬学部
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入江 寛
Faculty Of Pharmaceutical Sciences Kyoto University
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小山 淳子
Kobe Women's College of Pharmacy
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田中 祥子
Faculty Of Pharmaceutical Sciences Nagasaki University
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ZHANG YONG
Faculty of Pharmaceutical Sciences, Nagasaki University
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小山 淳子
神戸薬科大学
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小山 淳子
Kobe Women's College Of Pharmcy
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多賀 徹
Faculty Of Pharmaceutical Sciences Kyoto University
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町田 勝之輔
Faculty Of Pharmaceutical Sciences Kyoto University
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Zhang Y
Nagasaki Univ. Nagasaki Jpn
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Zhang Yong
Faculty Of Pharmaceutical Sciences Nagasaki University
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