Practical Synthesis of Optically Active Fluorine-substituted α-Phenylethylamines by Retardation of Hydrogenolytic Cleavage at Benzylic Position
スポンサーリンク
概要
- 論文の詳細を見る
- 2004-11-05
著者
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HIGASHIYAMA Kimio
Faculty of Medicinal Chemistry; Hoshi University
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Ishii Akihiro
Chemical Research Center Central Glass Co. Ltd.
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KANAI Masatomi
Chemical Research Center, Central Glass Co., Ltd.
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YASUMOTO Manabu
Chemical Research Center, Central Glass Co., Ltd.
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KURIYAMA Yokusu
Chemical Research Center, Central Glass Co., Ltd.
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INOMIYA Kenjin
Chemical Research Center, Central Glass Co., Ltd.
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KATSUHARA Yutaka
Chemical Research Center, Central Glass Co., Ltd.
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Kanai Masatomi
Chemical Research Center Central Glass Co. Ltd.
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Kuriyama Yokusu
Chemical Research Center Central Glass Co. Ltd.
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Inomiya Kenjin
Chemical Research Center Central Glass Co. Ltd.
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Yasumoto Manabu
Chemical Research Center Central Glass Co. Ltd.
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Katsuhara Yutaka
Chemical Research Center Central Glass Co. Ltd.
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Higashiyama Kimio
Faculty Of Pharmaceutical Science Hoshi University
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- Practical Synthesis of Optically Active Fluorine-substituted α-Phenylethylamines by Retardation of Hydrogenolytic Cleavage at Benzylic Position
- Stereospecific Reduction with Retention of Chiral Fluoral-derived 1, 3-Oxazolidines with LiAlH_4:Asymmetric Synthesis of 1-Substituted 2, 2, 2-Trifluoroethylamines