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Ru-Hydrogenation of Bulky Ketones with a Tridentate Ligand

机译:三齿配体对大分子酮进行钌加氢

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Current asymmetric hydrogena-tion catalysts for ketones typically involve[RuCl_2(diphos)(diamine)] systems, related to earli-er catalysts developed by Noyori. While highly ef-fective for most substrate classes, severe limita-tions are encountered with sterically encumberedketones. To overcome this problem, the authorshave synthesized complex 1, possessing a triden-tate P^N^NH_2-type ligand which is thought toprovide a more open coordination environment.With this system, various bulky ketone substratesare reduced in excellent yields and moderate tohigh enantioselectivities under hydrogenation ortransfer hydrogenation parameters.
机译:当前用于酮的不对称氢化催化剂通常涉及[RuCl_2(diphos)(diamine)]体系,与由Noyori开发的早期催化剂有关。尽管对于大多数底物类别都非常有效,但空间阻碍性酮会遇到严重的局限性。为了克服这个问题,作者合成了具有三价P ^ N ^ NH_2型配体的合成配合物1,认为该配体提供了更开放的配位环境。通过该系统,各种大体积的酮底物均具有良好的收率和中等至高的对映选择性在氢化或转移氢化参数下。

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