文献类型： 外文期刊
作者： Mu, Yangxiu 1 ; Yang, Minghua 2 ; Li, Fengxia 1 ; Iqbal, Zafar 1 ; Jiang, Rui 1 ; Hou, Jing 1 ; Guo, Xin 3 ; Yang, Zhixia 1 ;
作者机构： 1.Ningxia Acad Agr & Forestry Sci, Agr Resource & Environm Inst, Yinchuan 750002, Ningxia, Peoples R China
2.Lishui Univ, Dept Chem, Lishui 323000, Peoples R China
3.North Minzu Univ, Dept Pharmaceut Engn, Sch Chem & Chem Engn, Yinchuan 750002, Ningxia, Peoples R China
期刊名称：NEW JOURNAL OF CHEMISTRY （ 影响因子：3.288； 五年影响因子：3.153 ）
ISSN： 1144-0546
年卷期： 2021 年 45 卷 11 期
页码：
收录情况： SCI
摘要： An efficient sulfuration of isoquinolin-1(2H)-ones at the C-4 position is reported by employing ethyl sulfinates, and the corresponding products are obtained in moderate to excellent yields in the presence of iodine. This synthetic strategy provides a range of thioether-isoquinolin-1(2H)-ones while tolerating a number of functional groups on the isoquinoline nitrogen atom and benzene ring. In addition, pyridin-2(1H)-one is also reacted smoothly and afforded the corresponding thioether product in moderate yield. A plausible mechanism is suggested based on the preliminary mechanistic studies.
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