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首页> 外文期刊>Inorganica Chimica Acta >Synthesis, characterization and application of Ru(BINAP)(Acac)(MNAA)(MeOH), a highly effective catalyst for the asymmetric hydrogenation of 2-(6 '-methoxynaphth-2 '-yl)acrylic acid
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Synthesis, characterization and application of Ru(BINAP)(Acac)(MNAA)(MeOH), a highly effective catalyst for the asymmetric hydrogenation of 2-(6 '-methoxynaphth-2 '-yl)acrylic acid

机译:Ru(BINAP)(Acac)(MNAA)(MeOH)的合成,表征和应用-一种高效的2-(6'-甲氧基萘-2'-基)丙烯酸不对称加氢催化剂

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摘要

Ru(S-BINAP) (Acac) (MNAA) (MeOH) (1) (where MNAA (2) = 2-(6'-methoxynaphth-2'-yl) acrylate anion), a highly effective catalyst for the asymmetric hydrogenation of 2-(6'-methoxynaphth-2'-yl) acrylic acid (3)!, was isolated from a dichloromethane/methanol (vol./vol. = 1/4) solution of Ru(S-BINAP) (Acac), and excess of 2-(6'-methoxynaphth-2'-yl)acrylic acid after the solution was exposed to visible light for 2 weeks. On side by side comparison studies, the rate of the hydrogenation of 3 catalyzed by 1 was found to be substantially faster than the same reaction catalyzed by Ru(S-BINAP) (OAc)(2). The molecular structure of 1 was unambiguously characterized by single crystal X-ray diffraction. (C) 1998 Elsevier Science S.A. [References: 20]
机译:Ru(S-BINAP)(Acac)(MNAA)(MeOH)(1)(其中MNAA(2)= 2-(6'-甲氧基萘-2'-基)丙烯酸酯阴离子),一种用于不对称氢化的高效催化剂从Ru(S-BINAP)(Acac)的二氯甲烷/甲醇(体积/体积= 1/4)溶液中分离出2-(6'-甲氧基萘-2'-基)丙烯酸(3)!将溶液暴露于可见光2周后,再加入过量的2-(6'-甲氧基萘-2'-基)丙烯酸。并排比较研究发现,由1催化的3的氢化速率明显快于由Ru(S-BINAP)(OAc)(2)催化的相同反应。 1的分子结构通过单晶X射线衍射明确地表征。 (C)1998 Elsevier Science S.A. [参考:20]

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