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新兴的噻唑及其衍生物的绿色合成途径:当前的观点。

Emerging green synthetic routes for thiazole and its derivatives: Current perspectives.

机构信息

Faculty of Pharmacy, Ramanbhai Patel College of Pharmacy, Charotar University of Science and Technology, Anand, Gujarat, India.

Department of Fiber and Polymer Science, North Carolina State University, Raleigh, North Carolina, USA.

出版信息

Arch Pharm (Weinheim). 2024 Feb;357(2):e2300420. doi: 10.1002/ardp.202300420. Epub 2023 Nov 27.

Abstract

This review article provides an overview of the green synthesis of thiazole derivatives, emphasizing sustainable and environmentally friendly methodologies. Thiazole derivatives possess significant value and find diverse applications across various fields. However, conventional synthesis methods often involve hazardous reagents and generate substantial waste, posing environmental concerns. The green synthesis of thiazole derivatives employs renewable starting materials, nontoxic catalysts, and mild reaction conditions to minimize environmental impact. Innovative techniques such as microwave irradiation, ultrasound synthesis, green solvents, a green catalyst-based approach, and mechanochemistry-mediated synthesis are employed, offering advantages in terms of scalability, cost-effectiveness, and purification simplicity. The resulting thiazole derivatives exhibit comparable or enhanced biological activities, showcasing the feasibility and practicality of green synthesis in drug discovery. This review paper underscores the importance of sustainable approaches in functional molecular synthesis and encourages further research in this domain.

摘要

本文综述了噻唑衍生物的绿色合成方法,重点介绍了可持续和环保的方法学。噻唑衍生物具有重要的价值,在各个领域有广泛的应用。然而,传统的合成方法通常涉及危险试剂,并产生大量废物,对环境造成影响。噻唑衍生物的绿色合成采用可再生起始原料、无毒催化剂和温和的反应条件,以最小化环境影响。采用了一些创新技术,如微波辐射、超声合成、绿色溶剂、基于绿色催化剂的方法和机械化学介导的合成,在可扩展性、成本效益和纯化简单性方面具有优势。所得到的噻唑衍生物表现出相当或增强的生物活性,展示了绿色合成在药物发现中的可行性和实用性。本文强调了在功能分子合成中采用可持续方法的重要性,并鼓励在这一领域进一步研究。

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