Green and Sustainable Technology: Efficient Strategy for Synthesis of Biologically Active Pyrimidine Derivatives

IF 0.9 Q4 CHEMISTRY, PHYSICAL
B. Sahoo, B. R. Kumar, Krishna Chandra Panda, J. Sruti, A. Tiwari, S. Patra
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引用次数: 0

Abstract

Green chemistry is also referred as sustainable technology which involves the design, synthesis, processing and use of chemical substances by reducing or eliminating the chemical hazards. This strategy focuses on atom economy, use of safer solvents or chemicals, use of raw materials from renewable resources, consumption of energy and decomposition of the chemical substances to non-toxic material which are eco-friendly. So, this technology is utilized for the sustainable development of novel heterocyclic scaffold like pyrimidine derivatives. Pyrimidine is a six membered heterocyclic aromatic compound with two nitrogen atoms at positions 1 and 3 in the ring system. Among the other heterocyclic compounds, pyrimidine derivatives plays major role due to their diverse promising biological activities such as antimicrobial, antifungal, anti-viral, anti-tubercular, anti-diabetic, anti-hypertensive, anticancer, anthelmintic, antioxidant, anti-epileptic, antipsychotic, anti-anxiety, antimalarial, antihistaminic, anti-parkinsonian, analgesic and anti-inflammatory etc. The various green methods used for synthesis of pyrimidine derivatives include microwave assisted synthesis, ultrasound induced synthesis, ball milling technique, grinding technique, photo-catalysis. These processes enhance the rate of the reaction which leads to high selectivity with improved product yields as compared to the conventional synthetic methods. This review is focused on the green synthesis of biologically active pyrimidine derivatives.
绿色与可持续技术:生物活性嘧啶衍生物合成的高效策略
绿色化学也被称为可持续发展的技术,它涉及化学物质的设计、合成、加工和使用,以减少或消除化学危害。这一战略的重点是原子经济、使用更安全的溶剂或化学品、使用来自可再生资源的原材料、消耗能源和将化学物质分解为无害环境的无毒材料。因此,该技术可用于新型杂环支架如嘧啶衍生物的可持续开发。嘧啶是一种六元杂环芳香族化合物,在环系的1号和3号位置上有两个氮原子。在杂环类化合物中,嘧啶衍生物具有抗菌、抗真菌、抗病毒、抗结核、抗糖尿病、抗高血压、抗癌、驱虫药、抗氧化、抗癫痫、抗精神病、抗焦虑、抗疟疾、抗组胺、抗帕金森病、镇痛和抗炎等多种生物活性,具有重要作用。用于合成嘧啶衍生物的各种绿色方法包括微波辅助合成、超声诱导合成、球磨技术、研磨技术、光催化等。与传统的合成方法相比,这些方法提高了反应的速度,从而提高了产品收率和高选择性。本文对具有生物活性的嘧啶衍生物的绿色合成进行了综述。
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来源期刊
Current Organocatalysis
Current Organocatalysis CHEMISTRY, PHYSICAL-
CiteScore
2.00
自引率
0.00%
发文量
28
期刊介绍: Current Organocatalysis is an international peer-reviewed journal that publishes significant research in all areas of organocatalysis. The journal covers organo homogeneous/heterogeneous catalysis, innovative mechanistic studies and kinetics of organocatalytic processes focusing on practical, theoretical and computational aspects. It also includes potential applications of organocatalysts in the fields of drug discovery, synthesis of novel molecules, synthetic method development, green chemistry and chemoenzymatic reactions. This journal also accepts papers on methods, reagents, and mechanism of a synthetic process and technology pertaining to chemistry. Moreover, this journal features full-length/mini review articles within organocatalysis and synthetic chemistry. It is the premier source of organocatalysis and synthetic methods related information for chemists, biologists and engineers pursuing research in industry and academia.
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