BIOMIMETIC SYNTHESIS OF NAUCLEA INDOLE ALKALOIDS, NAUCLEIDINAL, AND 3-EPI-NAUCLEIDINAL, BY STEREOSELECTIVE REARRANGEMENT OF STRICTOSAMIDE AND THE VINCOSIDE LACTAM AGLYCONES
スポンサーリンク
概要
- 論文の詳細を見る
Based on a biogenetic consideration, a Nauclea alkaloid, naucleidinal (6), and its 3-epimer (7) were stereoselectively prepared from the aglycones of strictosamide and the vincoside lactam, and their absolute stereochemistry was confirmed.
- 社団法人日本薬学会の論文
- 1996-11-15
著者
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高山 廣光
Graduate School Of Pharmaceutical Sciences Chiba Univ.
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TAKAYAMA Hiromitsu
Research Center of Medicinal Resources, Faculty of Pharmaceutical Sciences, Chiba University
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KITAJIMA Mariko
Research Center of Medicinal Resources, Faculty of Pharmaceutical Sciences, Chiba University
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AIMI Norio
Research Center of Medicinal Resources, Faculty of Pharmaceutical Sciences, Chiba University
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MIYABE Yuhko
Research Center of Medicinal Resources, Faculty of Pharmaceutical Sciences, Chiba University
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SHITO Toshiaki
Research Center of Medicinal Resources, Faculty of Pharmaceutical Sciences, Chiba University
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Takayama Hiromitsu
Laboratory Of Molecular Structure And Biological Function Graduate School Of Pharmaceutical Sciences
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Aimi N
Graduate School Of Pharmaceutical Sciences Chiba University
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Miyabe Y
Research Center Of Medicinal Resources Faculty Of Pharmaceutical Sciences Chiba University
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Shito T
Research Center Of Medicinal Resources Faculty Of Pharmaceutical Sciences Chiba University
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Kitajima M
Department Of Biofunctional Molecular Chemistry Graduate School Of Pharmaceutical Sciences Chiba Uni
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