首页> 外文期刊>Bulletin of the Korean Chemical Society >Superior Effect of Ultrasonic Homogenization to Mechanical Agitation on Accelerating Reaction Rates in Asymmetric Ring Opening of Epoxides
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Superior Effect of Ultrasonic Homogenization to Mechanical Agitation on Accelerating Reaction Rates in Asymmetric Ring Opening of Epoxides

机译:超声均匀化对加速反应率的超声均匀化对环氧化物不对称开环加速反应速率的效果

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Double-layered mesoporous silica was prepared for use as an efficient support for the encapsulation of chiral salen Co-BF3 complexes in the pore channels. The heterogenized chiral salen complex was applied successfully to the asymmetric ring opening (ARO) of terminal epoxides using water, alcohols, and carboxylic acids as nucleophiles. Although the homogeneous salen catalyst exhibited higher catalytic activity than the heterogenized catalyst in ARO reactions as expected, the heterogeneous salen catalysts exhibited high catalytic activities that were sufficient for practical applications. This study evaluated the unique contribution of ultrasonic irradiation as a powerful mixing medium to improve the kinetics in comparison to conventional mechanical agitation during the ARO reactions. Both the homogeneous and heterogeneous chiral salen complexes catalyzed enantioselectively the racemic or chiral epoxides under ultrasonication. The adoption of ultrasonic irradiation in the catalysis resulted in a superior mixing effect to vigorous mechanical stirring. The reaction time was shortened to obtain the highest enantiomeric excess (% ee) when ultrasonic irradiation was applied to the reaction system. Through the ARO reaction of epoxide by phenol derivatives, the highly enantio-enriched beta-blockers could be synthesized easily from racemic terminal epoxides or chiral ones using chiral cobalt-salen catalysts. The regioselective ARO reaction of (R)ECH with propionic or butyric acid proceeded smoothly at room temperature under ultrasonic exposure in the presence of the heterogenized catalyst. The corresponding glycidyl alkylates were produced with excellent optical purity of up to 98% ee. The chiral cobalt-salen complexes encapsulated in MCM-41 retained its catalytic activity and enantioselectivity for three recycles. Consequently, the heterogeneous chiral catalysts anchored in MCM-41 offered the practical advantages of facile reuse through simple recovery from the reactant and products.
机译:制备双层介孔二氧化硅,以用作孔通道中的手性盐酸Co-BF3复合物的有效载体。使用水,醇和羧酸作为亲核试剂成功地应用于末端环氧化物的不对称环开口(ARO)的异源性手性盐化合物。尽管均匀的盐催化剂如预期的那样表现出比异丙化反应中的异质化催化剂更高的催化活性,但是异质的盐催化剂表现出高催化活性,这足以进行实际应用。该研究评估了超声波照射作为强大的混合培养基的独特贡献,以改善动力学与常规机械搅拌在ARO反应期间。均匀和异质的手性盐选络合物催化在超声波下对外消旋或手性环氧化物致致致致致倾向。在催化中采用超声波照射导致剧烈混合效果以剧烈的机械搅拌。当超声辐射施加到反应体系时,缩短反应时间以获得最高对映体过量(%EE)。通过苯酚衍生物环氧化物的ARO反应,使用手性钴 - 盐催化剂可以容易地从外消旋末端环氧化物或手性中合成高肾上腺β-嵌体。 (R)ech与丙酸或丁酸的区域反应在超声催化剂存在下在室温下平稳地进行。相应的缩水甘油基烷基化物以优异的光学纯度生产高达98%EE。包封在MCM-41中的手性钴 - 盐复合物保留其催化活性和对映的辅助切片,用于三次回收。因此,在MCM-41中锚定的异质性手性催化剂通过从反应物和产物的简单回收来提供容易再利用的实际优点。

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