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Application of NMI-TfCl-mediated amide bond formation in the synthesis of biologically relevant oxadiazole derivatives employing less basic (hetero)aryl amines
Molecular Diversity ( IF 3.9 ) Pub Date : 2021-07-22 , DOI: 10.1007/s11030-021-10275-7
Merla Arjuna Rajendra 1 , Muhammad Naseem 2 , Muthipeedika Nibin Joy 3 , K Sunil 1 , Ayyiliath Meleveetil Sajith 4 , Fares Howari 2 , Yousef Nazzal 2 , Cijo Xavier 2 , Mohammed B Alshammari 5 , Karickal Raman Haridas 4
Affiliation  

We herein report a modified methodology for the synthesis of some oxadiazoles linked to amides under mild conditions. The developed protocol using NMI-TfCl has been found to be effective and tolerant for the amide bond formation reaction of a series of electronically deactivating and sterically challenging amines. The antioxidant potential of the newly synthesized compounds has been evaluated at the later stage.

Graphic abstract



中文翻译:

NMI-TfCl 介导的酰胺键形成在使用弱碱性(杂)芳基胺合成生物学相关恶二唑衍生物中的应用

我们在此报告了一种改进的方法,用于在温和条件下合成一些与酰胺连接的恶二唑。已发现使用 NMI-TfCl 开发的协议对一系列电子失活和空间挑战性胺的酰胺键形成反应有效且耐受。新合成的化合物的抗氧化潜力已在后期进行了评估。

图形摘要

更新日期:2021-07-23
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