Canudo-Barreras Guillermo, Herrera Raquel P, Concepción Gimeno M
Laboratorio de Organocatálisis Asimétrica, Dpto. de Química Orgánica, Instituto de Síntesis Química y Catálisis Homogénea (ISQCH), CSIC-Universidad de Zaragoza, C/ Pedro Cerbuna N12, E-50009, Zaragoza, Spain.
Dpto. de Química Inorgánica, Instituto de Síntesis Química y Catálisis Homogénea (ISQCH), CSIC-Universidad de Zaragoza, C/ Pedro Cerbuna N12, E-50009, Zaragoza, Spain.
Chemistry. 2024 Oct 11;30(57):e202402812. doi: 10.1002/chem.202402812. Epub 2024 Sep 23.
This study introduces a sustainable and pioneering cascade synthesis of 1,3-thiazolidine derivatives under eco-friendly conditions. The methodology transcends traditional approaches yielding complex novel compounds with unique N,S-heterocyclic structures. By operating at room temperature, utilizing green solvents, and minimizing excess of reactants, this procedure offers an innovative pathway for sustainable chemical development. Notably, this method not only prioritizes sustainability but also delivers high-purity products with exceptional yields. The simplicity of the process, requiring only a simple filtration and featuring short reaction times, underscores its efficiency and utility.
本研究介绍了一种在环保条件下可持续且具有开创性的1,3-噻唑烷衍生物级联合成方法。该方法超越了传统方法,可生成具有独特N,S-杂环结构的复杂新型化合物。通过在室温下操作、使用绿色溶剂并尽量减少反应物过量,该过程为可持续化学发展提供了一条创新途径。值得注意的是,该方法不仅优先考虑可持续性,还能以优异的产率提供高纯度产品。该过程简单,仅需简单过滤且反应时间短,突出了其效率和实用性。