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AgNO3 as Nitrogen Source for Cu-Catalyzed Cyclization of Oximes with Isocyanates: A Facile Route to N-2-Aryl-1,2,3-triazoles
Organic Letters ( IF 5.2 ) Pub Date : 2021-08-30 , DOI: 10.1021/acs.orglett.1c02323
Jingwen Liang 1 , Yingqi Rao 1 , Weidong Zhu 1 , Tingting Wen 1 , Junjie Huang 1 , Zhichao Chen 1 , Lu Chen 1 , Yibiao Li 1 , Xiuwen Chen 1 , Zhongzhi Zhu 1
Affiliation  

A versatile copper-catalyzed [3 + 1 + 1] annulation of oximes and isocyanates with AgNO3 is described. In this conversion, AgNO3 and isocyanates instead of conventional azide or diazonium reagents were used as the nitrogen source. This three-component transformation was achieved by cleaving N–O/C–H/C–N bonds and building C═N/N–N bonds, which provides a strategy to prepare N-2-aryl-1,2,3-triazoles with a good substrate and functional compatibility.

中文翻译:

AgNO3 作为氮源用于铜催化异氰酸酯环化肟类化合物:生成 N-2-Aryl-1,2,3-三唑的简便途径

描述了一种多功能的铜催化 [3 + 1 + 1] 肟和异氰酸酯与 AgNO 3的环化。在该转化中,AgNO 3和异氰酸酯代替传统的叠氮化物或重氮试剂被用作氮源。这种三组分转化是通过裂解 N-O/C-H/C-N 键和构建 C=N/N-N 键来实现的,这为制备N -2-芳基-1,2,3-提供了一种策略三唑类具有良好的底物和功能相容性。
更新日期:2021-09-17
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