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Chiral Thiazolidine based Organocatalysts: Synthesis and Application in Asymmetric Aldol Reactions

机译:基于手性噻唑烷基的有机催化剂:在不对称醛醇反应中的合成和应用

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Several novel chiral organocatalysts derived from thiazolidines containing amide and thioureia functionalities were synthesized in good yields. These organocatalysts were tested in the asymmetric aldol reaction of acetone with p-nitrobenzaldehyde. Reaction parameters such as reaction time, catalyst loading and solvent were optimized. Products with conversions up to 84% and enantiomeric ratios (er) up to 84.5:15.5 (R:S) were obtained. The effect of several chiral and non-chiral additives on the reactivity and selectivity of the reaction was also evaluated. The reaction was extended to other aromatic aldehydes with the best organocatalyst and when p-bromobenzaldehyde was used, an er of 94.5:5.5 (R:S) was obtained.
机译:源自含有酰胺和硫脲官能团的甲硝素衍生的几种新型手性有机催化剂以良好的产率合成。 将这些有机催化剂在丙酮的不对称醛醇反应与p-硝基苯甲醛中进行测试。 优化反应参数,例如反应时间,催化剂负载和溶剂。 将转化的产品高达84%,对映体比(ER)高达84.5:15.5(R:S)。 还评价了几种手性和非手性添加剂对反应反应性和选择性的影响。 将反应延伸到具有最佳有机催化剂的其他芳香醛,并且当使用P-溴苯甲醛时,获得94.5:5.5(R:S)的ER。

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