Chen Mei-Tong, Li Yao-Rong, Wang Zhao-Qi, Jiang Shan, Jia Zan-Hui, Zhang Da-Wei
The Second Hospital of Jilin University, Changchun 130041, China.
College of Plant Science, Jilin University, Changchun 130062, China.
Pharmaceuticals (Basel). 2025 Aug 10;18(8):1179. doi: 10.3390/ph18081179.
Isoxazole-based molecules constitute a crucial category of heterocyclic compounds with wide-ranging applications across pharmaceutical development, advanced materials, and pesticide synthesis. Traditional synthetic approaches for isoxazole derivatives frequently encounter challenges such as extended reaction periods, severe operating conditions, and reliance on toxic solvents. As an eco-friendly alternative, sonochemistry has emerged as a promising approach for organic synthesis, offering enhanced reaction efficiency, reduced energy consumption, and improved yields. In this context, this review introduces the recent advancements in ultrasound-assisted strategies for the synthesis of isoxazole-scaffolds and their derivatives. Various methodologies are discussed, including multi-component reactions, catalytic systems, and solvent-free protocols. The integration of ultrasound not only accelerates reaction kinetics but also minimizes byproduct formation and enables the use of green solvents or catalysts. Key advantages such as shorter reaction durations, higher atom economy, and operational simplicity are emphasized. This work underscores the potential of sonochemical techniques to revolutionize isoxazole-based molecule synthesis, aligning with the principles of sustainable and green chemistry.
基于异恶唑的分子是一类至关重要的杂环化合物,在药物研发、先进材料和农药合成等领域有着广泛应用。传统的异恶唑衍生物合成方法常常面临反应时间长、操作条件苛刻以及依赖有毒溶剂等挑战。作为一种环保替代方法,声化学已成为有机合成中一种很有前景的方法,具有提高反应效率、降低能耗和提高产率等优点。在此背景下,本综述介绍了超声辅助合成异恶唑骨架及其衍生物策略的最新进展。讨论了各种方法,包括多组分反应、催化体系和无溶剂方案。超声的引入不仅加快了反应动力学,还减少了副产物的形成,并能够使用绿色溶剂或催化剂。强调了反应时间短、原子经济性高和操作简便等关键优势。这项工作强调了声化学技术在革新基于异恶唑的分子合成方面的潜力,符合可持续和绿色化学的原则。