Asymmetric Synthesis of (R)-Nilvadipine and (S)-NB 818 via Regioselective Bromination of Chiral 1,4-Dihydropyridines as a Key Step and Enzymatic Resolution of Racemic 2-Hydroxymethyl-1,4-dihydropyridine Derivatives
スポンサーリンク
概要
- 論文の詳細を見る
Optically active 2-hydroxymethyl-1,4-dihydropyridines were obtained by lipase-catalyzed hydrolysis or transesterification of racemic materials. Chiral NB 818 and nilvadipine have been synthesized from chiral 2-hydroxymethyl-1,4-dihydropyridine. On the other hand, chiral 1,4-dihydropyridines obtained from prochiral substrates have been converted into (S)-NB 818 and (R)-nilvadipine via regioselective bromination of methyl groups under mild conditions.
- 公益社団法人日本薬学会の論文
- 1997-05-15
著者
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阿知波 一雄
静岡県立大学薬学部
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阿知波 一雄
School of Pharmaceutical Sciences, University of Shizuoka
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阿知波 一雄
静岡県大薬
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阿知波 一雄
東大・薬
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Maruyama K
帝京大学 薬 薬剤
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Yamazaki Yohko
微生物化学研究会微生物化学研究センター沼津創薬医科学研究所
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ACHIWA Kazuo
School of Pharmaceutical Sciences, University of Shizuoka
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Yamazaki Yoko
Numazu Bio-medical Research Institute Microbial Chemistry Research Center
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Achiwa Kazuo
School Of Pharmaceutical Sciences University Of Shizuoka
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Achiwa Kazuo
School Of Pharmaceutical Sciences(laboratory Of Medicinal Chemistry)
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EBIIKE Hirosato
School of Pharmaceutical Sciences, University of Shizuoka
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MARUYAMA Kaori
School of Pharmaceutical Sciences, University of Shizuoka
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OZAWA Yumi
School of Pharmaceutical Sciences, University of Shizuoka
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YAMAZAKI Yukiyoshi
School of Pharmaceutical Sciences, University of Shizuoka
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Ebiike H
School Of Pharmaceutical Sciences University Of Shizuoka
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Ebiike Hirosato
School Of Pharmaceutical Sciences University Of Shizuoka
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Ozawa Y
School Of Pharmaceutical Sciences University Of Shizuoka
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桐山 美由紀
Meiji Pharmaceutical Univ. Tokyo Jpn
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Maruyama K
Kyoto Pharmaceutical University
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山嵜 行由
School Of Pharmaceutical Sciences University Of Shizuoka
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