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首页> 外文期刊>Applied Organometallic Chemistry >Ruthenium(II) complexes derived from C-2-symmetric ferrocene-based chiral bis(phosphinite) ligands: synthesis and catalytic activity towards the asymmetric reduction of acetophenones
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Ruthenium(II) complexes derived from C-2-symmetric ferrocene-based chiral bis(phosphinite) ligands: synthesis and catalytic activity towards the asymmetric reduction of acetophenones

机译:C-2-对称二茂铁基手性双(次膦酸酯)配体的钌(II)配合物:对苯乙酮的不对称还原的合成和催化活性

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摘要

Chiral secondary alcohols are very important building blocks and valuable synthetic intermediates both in organic synthesis and in the pharmaceutical industry for producing biologically active complex molecules. A series of new chiral Ru-phosphinite complexes (1, 2, 3, 4, 5, 6, 7, 8) were prepared from chiral C-2-symmetric ferrocenyl phosphinites and corresponding chloro complex, [Ru((6)-p-cymene)(-Cl)Cl](2). The complexes were characterized using conventional spectroscopic methods. The binuclear complexes were tested as pre-catalysts and were found to be good pre-catalysts for the asymmetric transfer hydrogenation of substituted acetophenones in basic 2-propanol at 82 degrees C, providing the corresponding optically active alcohols with almost quantitative conversion and modest to high enantioselectivities (46-97%). Amongst the all complexes, complex 6 gave the highest ee of 97% in the reduction of 2-methoxyacetophenone to (S)-1-(2-methoxyphenyl)ethanol at 82 degrees C. Copyright (c) 2015 John Wiley & Sons, Ltd.
机译:在有机合成和制药工业中,手性仲醇是非常重要的结构单元和有价值的合成中间体,用于生产具有生物活性的复合分子。由手性C-2-对称二茂铁基亚膦酸酯和相应的氯配合物[Ru((6)-p)制备一系列新的手性Ru-次膦酸酯络合物(1、2、3、4、5、6、7、8) -cymene)(-Cl)Cl](2)。使用常规光谱法表征复合物。该双核络合物已作为前催化剂进行了测试,被发现是在82°C下碱性2-丙醇中取代的苯乙酮不对称转移氢化的良好预催化剂,提供了几乎定量转化且适度转化为高分子量的相应旋光醇。对映选择性(46-97%)。在所有配合物中,配合物6在82摄氏度下将2-甲氧基苯乙酮还原为(S)-1-(2-甲氧基苯基)乙醇时,ee最高,为97%。版权所有(c)2015 John Wiley&Sons,Ltd 。

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