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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Asymmetric synthesis of (R)-(+)-6-(1,4-dimethoxy-3-methyl-2-naphthyl)-6-(4-hydroxyphenyl)hexanoic acid as a key intermediate for a neurodegenerative disease agent
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Asymmetric synthesis of (R)-(+)-6-(1,4-dimethoxy-3-methyl-2-naphthyl)-6-(4-hydroxyphenyl)hexanoic acid as a key intermediate for a neurodegenerative disease agent

机译:(R)-(+)-6-(1,4-二甲氧基-3-甲基-2-萘基)-6-(4-羟苯基)己酸的不对称合成作为神经退行性疾病药物的关键中间体

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An asymmetric synthesis of (R)-(+)-6-(1,4-dimethoxy-3-methyl-2-naphthyl)-6-(4-hydroxyphenyl)hexanoic acid 2 as a key intermediate for a neurodegenerative disease agent 1 has been developed. A key reaction was an asymmetric hydrogenation of hindered acrylic acid 13 catalyzed by the Rh-JOSIPHOS system in the presence of a base to afford a chiral acid up to 93% ee. (C) 2004 Elsevier Ltd. All rights reserved.
机译:不对称合成(R)-(+)-6-(1,4-二甲氧基-3-甲基-2-萘基)-6-(4-羟苯基)己酸2作为神经退行性疾病药物1的关键中间体已经被开发出来。关键反应是在碱的存在下,由Rh-JOSIPHOS系统催化的受阻丙烯酸13的不对称氢化,可提供高达93%ee的手性酸。 (C)2004 Elsevier Ltd.保留所有权利。

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