Asymmetric Hydrolysis of (dl)-1-Acyloxy-2-halo-1-phenylethanes with Lipases(Organic Chemistry)
スポンサーリンク
概要
- 論文の詳細を見る
Asymmetric hydrolysis of (dl)-l-acyloxy-2-halo-l-phenylethanes by lipoprotein lipase Amano P from Pseudomonas fluorescens and the lipase from Chromobacterium viscosum afforded the optically active (R) residual substrates and (S)-2-halo-l-hydroxy-l-phenylethanes in 100% enantiomeric excess (e.e.). The length of acyl residues from acetyl to octanoyl in the substrates did not influence the enantioselectivity. Both enantiomers of optically active styrene oxides were synthesized from the enzymatic products.
- 社団法人日本農芸化学会の論文
- 1986-09-23
著者
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Hasegawa J
Biochemical Research Laboratories Kanegafuchi Chemical Industry Co. Ltd.
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WATANABE Kiyoshi
Biochemical Research Laboratories, Kanegafuchi Chemical Industry Co., Ltd.
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Hasegawa J
Fine Chemicals Research Laboratories Kaneka Corporation
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Hasegawa J
Kaneka Corp. Hyogo Jpn
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HASEGAWA Junzo
Biochemical Research Laboratories, Kanegafuchi Chemical Industry Co., Ltd.
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KUTSUKI Hidetoshi
Biochemical Research Laboratories, Kanegafuchi Chemical Industry Co., Ltd.
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SAWA Ikuo
Biochemical Research Laboratories, Kanegafuchi Chemical Industry Co., Ltd.
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Sawa Ikuo
Fine Chemicals Research Laboratories Kaneka Corporation
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Sawa Ikuo
Biochemical Research Laboratories Kanegafuchi Chemical Industry Co. Ltd.
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Kutsuki Hidetoshi
Biochemical Research Laboratories Kanegafuchi Chemical Industry Co. Ltd.
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Hasegawa Junzo
Life Science R & D Center Kaneka Co.
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Hasegawa Junzo
Biochemical Research Laboratories Kanegafuchi Chemical Industry Co. Ltd.
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Watanabe Kiyoshi
Biochemical Research Laboratories Kanegafuchi Chemical Industry Co. Ltd.
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Watanabe K
Research Institute For Food Science Kyoto University:(present Address)department Of Agricultural Che
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