Weng Yunxiang, Min Lin, Shan Lidong, Li Hongchen, Wang Xinyan, Hu Yuefei
Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing 100084, P. R. China.
J Org Chem. 2021 Jan 1;86(1):199-206. doi: 10.1021/acs.joc.0c02015. Epub 2020 Dec 7.
A general and efficient synthesis of fully substituted 4-aminodixazoles was developed based on the strategies of amide activation and umpolung reaction. In this method, 1,4,2-dioxazol-5-ones were introduced as a rare type of umpolung reagent bearing a nucleophilic -atom that could be used well together with the activating agent TfO. Because 1,4,2-dioxazol-5-ones played triple roles as an umpolung reagent, a substrate, and a weak base, the method proceeded smoothly under extremely convenient conditions.
基于酰胺活化和极性翻转反应策略,开发了一种通用且高效的全取代4-氨基二恶唑的合成方法。在该方法中,引入了1,4,2-二恶唑-5-酮作为一种罕见的带有亲核原子的极性翻转试剂,它可以与活化剂三氟甲磺酸根很好地配合使用。由于1,4,2-二恶唑-5-酮同时扮演了极性翻转试剂、底物和弱碱这三种角色,该方法在极其简便的条件下顺利进行。