...
  • 主题
高级搜索  >
历史搜索 清空历史
首页> 外文期刊>Catalysis Communications >Transition metal-free and base-mediated transformation arylation of unactivated benzene with aryl halides in presence of N,N '-bis(salicylidene) ethylenediamine as organocatalyst
【24h】

Transition metal-free and base-mediated transformation arylation of unactivated benzene with aryl halides in presence of N,N '-bis(salicylidene) ethylenediamine as organocatalyst

机译：在N，N'-BIS（水杨烯）乙二胺作为有机催化剂存在下，无催化苯的无催化苯的无致活化苯的转化芳族

获取原文
获取原文并翻译 | 示例
           
页面导航
  • 摘要
  • 著录项
  • 相似文献
  • 相关主题

摘要

Direct transition metal-free arylation of benzene has been achieved using a combination of various aryl halides and N,N'-bis(salicylidene)ethylenediamine as a new ligand and catalyst. This facile one-pot reaction is reported as a new C-H functionalization protocol for the synthesis of biaryls. In this research, 18-crown-6 and several Schiff-bases were tested and among them, N,N'-bis(salicylidene)ethylenediamine was found to be a great catalyst for this cross-coupling.
机译：使用各种芳基卤化物和N，N'-BIS（水杨酸）乙二胺作为新配体和催化剂，实现了直接过渡无金属芳基苯的苯。 将该容易的单壶反应报告为合成前列的新型C-H官能化方案。 在本研究中，测试了18冠-6和几个席夫碱，其中N，N'-BIS（水杨烯）乙二胺被发现是该交叉偶联的巨大催化剂。

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