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Recent Advances in Green Synthesis of Functionalized Quinolines of Medicinal Impact (2018-Present)

机译:药用功能化喹啉绿色合成研究进展(2018-至今)

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The synthetic chemists are awakening to make substantial development in finding safer drugs against the rising communicable and non-communicable type of diseases. By replacing traditional methods to more sustainable and greener approaches, multicomponent reactions are the rapid and efficient tool for the synthesis of organic molecules of structural diversity and complexity. Heterocyclic chemistry transforms small set of precursors into series of molecules by multicomponent domino reactions. This review covers recent trends of last five years (2018-2022) in construction of potentially drug-like quinoline derivatives. The methods discussed here are preferable over conventional approaches being inexpensive, consuming lesser reaction time, atom economical, saving energy and manpower while avoiding toxic reagents/materials, chemical wastes and are environmental/occupational benign. The contributions covered here involve metallic, metal free strategies and other catalytic pathways including nanoparticles, ionic liquids and photocatalysis which are operationally safe and reliable.
机译:合成化学家正在觉醒,在寻找更安全的药物来对抗日益严重的传染性和非传染性疾病方面取得了重大进展。通过将传统方法替换为更可持续和更环保的方法,多组分反应是合成具有结构多样性和复杂性的有机分子的快速有效工具。杂环化学通过多组分多米诺骨牌反应将一小组前体转化为一系列分子。本综述涵盖了过去五年(2018-2022年)在构建潜在药物样喹啉衍生物方面的最新趋势。这里讨论的方法比传统方法更可取,价格低廉,消耗反应时间短,原子经济,节省能源和人力,同时避免有毒试剂/材料、化学废物,并且对环境/职业无害。这里涵盖的贡献涉及金属、无金属策略和其他催化途径,包括纳米颗粒、离子液体和光催化,这些途径在操作上是安全可靠的。

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