School of Chemical and Biomedical Engineering, Nanyang Technological University, 62 Nanyang Drive, N1.2-B1-14, Singapore 637459, Singapore.
J Org Chem. 2022 Sep 16;87(18):12115-12131. doi: 10.1021/acs.joc.2c01270. Epub 2022 Aug 31.
A one-pot, three-component cascade reaction between unprotected sugars, primary amines, and 3-oxoacetonitriles gave N-substituted 2,3,5-functionalized pyrroles or N-substituted 2,3,4-functionalized pyrroles in excellent yields and selectivities. The selectivity of the reaction was achieved by simple control of the sequence of substrate addition. The reaction showed a wide substrate scope, and various types of sugars, primary amines, and oxoacetonitriles reacted smoothly. The work demonstrates a highly desired simple reaction for embedding nitrogen into sugars to produce valuable N-heterocyclic compounds that are amenable to further modifications to natural products and drug intermediates.
一锅法、三组分级联反应将未保护的糖、伯胺和 3-氧代乙腈反应,以极好的收率和选择性得到 N-取代的 2,3,5-三取代吡咯或 N-取代的 2,3,4-三取代吡咯。通过简单控制底物添加顺序实现了反应的选择性。该反应底物范围广泛,各种类型的糖、伯胺和氧代乙腈都能顺利反应。该工作展示了一种非常理想的将氮嵌入糖中以生成有价值的含氮杂环化合物的简单反应,这些化合物可以进一步修饰为天然产物和药物中间体。