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Asymmetric transfer hydrogenation of ketones promoted by manganese(I) pre-catalysts supported by bidentate aminophosphines
Catalysis Communications ( IF 3.7 ) Pub Date : 2020-05-11 , DOI: 10.1016/j.catcom.2020.106040
Karim Azouzi , Antoine Bruneau-Voisine , Laure Vendier , Jean-Baptiste Sortais , Stéphanie Bastin

A series of commercially available chiral amino-phosphines, in combination with Mn(CO)5Br, has been evaluated for the asymmetric reduction of ketones, using isopropanol as hydrogen source. With the most selective ligand, the corresponding manganese complex was synthesized and fully characterized. A series of ketones (20 examples) was hydrogenated in the presence of 0.5 mol% of the manganese pre-catalyst at 30 °C, affording the chiral alcohols in high yields with enantiomeric excesses up to 99%.



中文翻译:

二齿氨基膦负载的锰(I)预催化剂促进的酮的不对称转移加氢

使用异丙醇作为氢源,已评估了一系列与Mn(CO)5 Br组合使用的手性氨基膦类化合物的酮的不对称还原。用最具选择性的配体合成了相应的锰配合物并进行了充分表征。将一系列酮(20个实例)在0.5摩尔%的锰预催化剂存在下于30°C氢化,以高收率得到手性醇,对映体过量最高可达99%。

更新日期:2020-05-11
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