首页> 外文期刊>Chemistry: A European journal >Efficient synthesis of biologically interesting 3,4-diaryl-substituted succinimides and maleimides: Application of iron-catalyzed carbonylations
【24h】

Efficient synthesis of biologically interesting 3,4-diaryl-substituted succinimides and maleimides: Application of iron-catalyzed carbonylations

机译:有效合成生物学上有趣的3,4-二芳基取代的琥珀酰亚胺和马来酰亚胺:铁催化羰基化的应用

获取原文
获取原文并翻译 | 示例
           

摘要

A straightforward two-step synthesis of trans-3,4-disubstituted succin imides through a palladium-catalyzed Sonogashira reaction and an iron-catalyzed double carbonylation is described. In situ oxidative dehydrogenation gave the corresponding 3,4-diarylmaleimides. By starting from readily available aryl and hetgeroaryl halides, a variety of new analogues and derivatives of bioactive 3,4-bisindolylmaleimides are obtained in good yield and selectivity.
机译:描述了通过钯催化的Sonogashira反应和铁催化的双羰基化的反式3,4-二取代的琥珀酰亚胺的直接两步合成法。原位氧化脱氢得到相应的3,4-二芳基马来酰亚胺。通过从容易获得的芳基和杂芳基卤化物开始,以良好的产率和选择性获得了多种新的具有生物活性的3,4-二吲哚基马来酰亚胺的类似物和衍生物。

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