首页> 外文期刊>RSC Advances >Synthesis of primary N-arylthioglyoxamides from anilines, elemental sulfur and primary C–H bonds in acetophenones
【24h】

Synthesis of primary N-arylthioglyoxamides from anilines, elemental sulfur and primary C–H bonds in acetophenones

机译:用苯胺,元素硫和初级C-H键合的原发性正芳基乙醛酰胺的合成

获取原文
           

摘要

A simple method for coupling of anilines, acetophenones, and elemental sulfur to afford N -arylthioglyoxamides has been developed. Reactions proceeded in the presence of Na _(2) SO _(3) and DMSO, thus eliminating the need for transition metals and external oxidants. Functionalities such as halogen, ester, methylthio, and heterocycle groups were compatible with the conditions. Electron-poor acetophenones sometimes gave isosteric glyoxamides.
机译:已经开发了一种简单的苯胺,苯苯酮和元素硫偶联以提供N-芳基血红素酰胺的简单方法。在Na _(2)所以_(3)和DMSO存在下进行的反应,从而消除了过渡金属和外氧化剂的需要。卤素,酯,甲硫基和杂环基等功能与条件相容。电子贫苯烯酮有时会赋予旁边甲酰胺。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号