1673-159X

CN 51-1686/N

脯氨酸衍生的咪唑手性离子液的合成及其在不对称Micheal反应中的应用

Synthesis of Imidazole Chiral Ionic Liquids Derived from Proline and Its Application in Asymmetry Micheal Reaction

  • 摘要: 离子液体(IL)具有较高的化学稳定性和溶解性、低毒、低挥发、不可燃、可循环等优点;天然氨基酸是一种重要的手性源分子,其中-脯氨酸是揭开有机小分子催化序幕的“明星分子”。鉴于此,本文以天然脯氨酸为手性源,设计并合成了一种结构新颖的咪唑类手性离子液,并将其应用于催化不对称Micheal加成,结果表明该新型脯氨酸衍生的咪唑类手性离子液具有良好的不对称催化性能和循环使用性能。

     

    Abstract: Ionic liquid (IL) has many advantages, such as high chemical stability and solubility, low toxicity, low volatile, non-combustible, recyclable etc. Natural amino acid is a kind of chiral source molecules, and L-proline is the star molecules because it reveals the organocatalysis prelude. In view of these, we synthesized a novel imidazole chiral ionic liquid with L-proline as chiral source. This new chiral ionic liquid was applied to catalyze the asymmetric Micheal addition. The results show that this imidazole chiral ionic liquid derived from proline has good asymmetric catalytic and recycling performance.

     

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