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AgNOx as Nitrogen Source for [1+1+3] Cycloaddition of Isocyanides with Isocyanates: Selective Synthesis of 1,2,4-Triazoles
Organic Letters ( IF 4.9 ) Pub Date : 2024-07-22 , DOI: 10.1021/acs.orglett.4c02130
Baihui Liang 1 , Tingting Wen 1 , Xiangya Cai 1 , Yutong Hu 1 , Biao Nie 2 , Weijie Ren 1 , Jiehao Chen 1 , Tsz Woon Benedict Lo 3 , Xiuwen Chen 1 , Zhongzhi Zhu 1
Affiliation  

A novel [1+1+3] annulation of AgNOx, isocyanides, and isocyanates for the selective synthesis of 1,2,4-triazoles is presented herein. In this transformation, AgNOx and isocyanates are used as nitrogen sources instead of the traditional hydrazine or diazonium reagents. This process also involves N–O/C–H/C═N bond cleavage and the construction of new N–N/C–N bonds with a good substrate scope and functional group tolerance.

中文翻译:


AgNOx 作为异氰酸酯与异氰酸酯的 [1+1+3] 环加成反应的氮源:1,2,4-三唑的选择性合成



本文提出了一种用于选择性合成 1,2,4-三唑的 AgNOx、异氰化物和异氰酸酯的新型 [1+1+3] 环化。在此转化中,AgNOx 和异氰酸酯用作氮源,而不是传统的肼或重氮试剂。该过程还涉及 N-O/C-H/C=N 键断裂以及具有良好底物范围和官能团耐受性的新 N-N/C-N 键的构建。
更新日期:2024-07-24
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