Total Synthesis of (±)-, (-)-, and (+)-Oudemansin X
スポンサーリンク
概要
- 論文の詳細を見る
Three kinds of oudemansin X, (-)-1,(+)-1 and (±)-1,were totally synthesized. The key point in the present chiral synthesis was the enantioselective acetylation of the racemic alcohols, (±)-5 and (±)-8,using lipase in an organic solvent. The synthetic (-)-1 was found to exhibit strong antifungal activity against several molds and yeasts.
- 社団法人日本薬学会の論文
- 1995-07-15
著者
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秋田 弘幸
School of Pharmaceutical Sciences, Toho University
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南雲 紳史
School Of Pharmaceutical Science Toho University
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Nagumo S
School Of Pharmaceutical Science Toho University
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梅澤 勲
School of Pharmaceutical Science, Toho University
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野澤 雅子
School of Pharmaceutical Science, Toho University
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Akita H
Toho Univ. Chiba Jpn
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秋田 弘幸
School Of Pharmaceutical Science Toho University
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Akita Hiroyuki
School Of Pharmaceutical Science Toho University
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梅澤 勲
School Of Pharmaceutical Science Toho University
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Nozawa M
Graduate School Of Pharmaceutical Sciences Chiba University
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野澤 雅子
School Of Pharmaceutical Science Toho University
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Nagumo S
Hokkaido Coll. Pharmacy Otaru Jpn
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Umezawa I
Riken Institute (the Institute Of Physical And Chemical Research):(present Address)fuji Yakuhin Co.
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