Kinetic Resolutions of Indan Derivatives Using Bacteria(Microbiology & Fermentation Technology)
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概要
- 論文の詳細を見る
Racemic indan derivatives have been resolved by the hydrolysis of amide bonds using Corynebacterium ammoniagenes IFO12612 to produce (S)-amine and (R)-amides. In the kinetic resolution of 1 (N-[2-(6-methoxyindan-l-yl)ethyl]acetamide), it was possible to run the reaction to 44% conversion on a 10-g scale, obtaining (S)-amine 4 ((S)-2-(6-methoxy-indan-1-yl)ethylamine) at > 99% enantiomeric excess (ee) and (R)-1 at 98% ee.
- 社団法人日本農芸化学会の論文
- 2002-02-23
著者
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OHKAWA Shigenori
Pharmaceutical Research Division, Takeda Pharmaceutical Company, Ltd.
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Tarui N
Takeda Chemical Ind. Ltd. Osaka Jpn
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Tarui Naoki
Pharmaceutical Research Division Takeda Chemical Industries Ltd.
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Nakahama Kazuo
Pharmaceutical Research Division Takeda Chemical Industries Ltd.
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Nakahama K
Pharmaceutical Research Division Takeda Chemical Industries Ltd.
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WATANABE Hayao
Pharmaceutical Research Division, Takeda Chemical Industries, Ltd.
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FUKATSU Kohji
Pharmaceutical Research Division, Takeda Chemical Industries, Ltd.
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Fukatsu K
Pharmaceutical Research Division Takeda Chemical Industries Ltd.
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Watanabe Hayao
Pharmaceutical Research Division Takeda Chemical Industries Ltd.
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Ohkawa Shigenori
Pharmaceutical Research Division Takeda Chemical Industries Ltd.
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