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Microwave-assisted diastereoselective two-step three-component synthesis for rapid access to drug-like libraries of substituted 3-amino-β-lactams
Bioorganic & Medicinal Chemistry ( IF 3.5 ) Pub Date : 2017-11-16 , DOI: 10.1016/j.bmc.2017.11.014
Guido V. Janssen , Joyce A.C. van den Heuvel , Rik P. Megens , Jorg C.J. Benningshof , Huib Ovaa

Large, diverse compound libraries are an essential requisite in target-based drug development. In this work, a robust microwave-assisted synthesis for the diastereoselective generation of 3-saccharinyl-trans-β-lactams is reported. The method is optimised for combinatorial library synthesis in which decoration of the scaffold is varied on both the β-lactam and the saccharine moiety. Within the European Lead Factory (ELF) consortium, a library of 263 compounds was efficiently produced using the developed methodology.



中文翻译:

微波辅助非对映选择性两步三组分合成,可快速访问取代的3-氨基-β-内酰胺类药物库

大型多样的化合物库是基于靶标的药物开发的基本要求。在这项工作中,报道了用于3-糖精基-反式-β-内酰胺的非对映选择性生成的稳健的微波辅助合成。该方法针对组合文库合成进行了优化,在该文库中,β-内酰胺和糖精部分的骨架修饰均发生变化。在欧洲铅厂(ELF)联盟中,使用开发的方法有效地生产了263种化合物的库。

更新日期:2017-11-16
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