Synthetic Anthracyclines : Total Synthesis of D-Ring Pyridine and Pyrazine Analogues of 11-Deoxydaunomycin
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概要
- 論文の詳細を見る
Treatment of sodium salts generated from tetrahydrohomophthalic anhydrides (6a, b) with 5,8-dihydro-5,8-dioxoquinoline (9) gave cycloadducts (7 and 8), regioselectively. These adducts were converted to the D-ring pyridine analogue (21) of 11-deoxydaunomycin. The D-ring pyrazine analogue (27) of 11-deoxydaunomycin was also prepared by a similar method.
- 社団法人日本薬学会の論文
- 1991-04-25
著者
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田村 恭光
Faculty Of Pharmaceutical Sciences Osaka University
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大石 宏文
Osaka University of Pharmaceutical Sciences
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石田 寿昌
Osaka University of Pharmaceutical Sciences
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桐原 正之
Faculty Of Pharmaceutical Sciences Osaka University
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北 泰行
Faculty of Pharmaceutical Sciences, Osaka University
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北 泰行
大阪大学大学院薬学研究科
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赤井 周司
大阪大学大学院薬学研究科
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Kita Yasuyuki
Graduate School Of Pharmaceutical Sciences Osaka University Yamadaoka
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前田 ひろし
Faculty of Pharmaceutical Sciences, Osaka University
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赤井 周司
Faculty of Pharmaceutical Sciences, Osaka University
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藤井 裕士
Faculty of Pharmaceutical Sciences, Osaka University
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奥仲 隆一
Faculty of Pharmaceutical Sciences, Osaka University
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下岡 釿雄
New Product Development Center, Pfizer Pharmaceutical Inc., Ltd.,
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藤井 裕士
Faculty Of Pharmaceutical Sciences Osaka University
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奥仲 隆一
Faculty Of Pharmaceutical Sciences Osaka University
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下岡 釿雄
New Product Development Center Pfizer Pharmaceutical Inc. Ltd.
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前田 ひろし
Faculty Of Pharmaceutical Sciences Osaka University
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北 泰行
Faculty Of Pharmaceutical Sciences Osaka University
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