A TOTAL AND PRACTICAL SYNTHESIS OF ERGOT ALKALOID, (±)-AURANTIOCLAVINE
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概要
- 論文の詳細を見る
The first synthesis of (±)-aurantioclavine by a convenient and practical five-step synthetic method, involving a new intra-molecular cyclization of nitro-olefin, is achieved starting from 3-formylindole with a 31% overall yield without using any protective groups.
- 1985-05-25
著者
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山田 文夫
金沢大薬
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鈴木 朋子
Faculty Of Pharmaceutical Sciences Kanazawa University
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染井 正徳
Faculty of Parmaceutical Sciences, Kanazawa University
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山田 文夫
Faculty of Pharmaceutical Sciences, Kanazawa University
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巻田 吉彦
Faculty of Pharmaceutical Sciences, Kanazawa University
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巻田 吉彦
Faculty Of Phermaceutical Sciences Kanazawa University
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巻田 吉彦
Faculty Of Pharmaceutical Sciences Kanazawa University
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