首页> 外文期刊>Journal of Catalysis >Chiral macrocyclic salen Mn(III) complexes catalyzed enantioselective epoxidation of non-functionalized alkenes using NaOCl and urea H _2O_2 as oxidants
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Chiral macrocyclic salen Mn(III) complexes catalyzed enantioselective epoxidation of non-functionalized alkenes using NaOCl and urea H _2O_2 as oxidants

机译:NaOCl和尿素H _2O_2作为氧化剂,手性大环赛伦Mn(III)配合物催化非官能化烯烃的对映选择性环氧化

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摘要

Two new chiral Mn(III) macrocyclic salen complexes 1a and 1b were prepared for the enantioselective epoxidation of non-functionalized alkenes. A 5 mol% loading of these catalysts in the presence of pyridine N-oxide as an axial base and sodium hypochlorite or urea hydrogen peroxide adduct as oxidant worked well to give respective epoxides in high yields and ee (up to >95% in selected cases). The catalyst 1b with urea hydrogen peroxide adduct as an oxidant was recovered by precipitation with hexane and was reused up to four times with retention of enantioselectivity.
机译:制备了两个新的手性Mn(III)大环萨伦配合物1a和1b,用于非官能化烯烃的对映选择性环氧化。在吡啶N-氧化物作为轴向碱,次氯酸钠或尿素过氧化氢加合物作为氧化剂的情况下,这些催化剂的5摩尔%负载效果很好,从而可以高收率和ee生成各自的环氧化物(在某些情况下高达> 95% )。通过用己烷沉淀回收具有脲过氧化氢加合物作为氧化剂的催化剂1b,并在保留对映选择性的情况下重复使用多达四次。

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