...
首页> 外文期刊>Advanced synthesis & catalysis >Efficient Modular Synthesis of Isomeric Mono- and Bispyridyl[2.2]paracyclophanes by Palladium-Catalyzed Cross- Coupling Reactions
【24h】

Efficient Modular Synthesis of Isomeric Mono- and Bispyridyl[2.2]paracyclophanes by Palladium-Catalyzed Cross- Coupling Reactions

机译:钯催化的交叉偶联反应高效模块化合成异构体单和双吡啶基[2.2]对环环烷

获取原文
获取原文并翻译 | 示例

摘要

Pyridyl-substituted [2.2]paracyclophanes build a multifunctional structural motif that is useful in material chemistry, catalysis and for luminescent structures. Nonetheless, there is still a lack of general methods for the synthesis of these structures tolerating easily accessible bromides as well as different isomeric pyridyl groups. Hence the coupling of functionalized [2.2]paracyclophanes with various substituted and functionalized pyridyl derivatives was achieved using Stille, Suzuki and Kumada coupling conditions. Hereby the Stille coupling of a [2.2]paracyclophane is presented as a versatile reaction for the formation of heteromeric [2.2]paracyclophane-containing biaryl structures.
机译:吡啶基取代的[2.2]对环环烷烃可形成多功能的结构基序,可用于材料化学,催化和发光结构。尽管如此,仍然缺乏用于合成这些易于耐受的溴化物以及不同的异构吡啶基的结构的通用方法。因此,使用Stille,Suzuki和Kumada偶联条件实现了官能化的[2.2]对环环烷与各种取代的和官能化的吡啶基衍生物的偶联。因此,[2.2]对环环烷的斯蒂勒偶联被呈现为用于形成包含异聚[2.2]对环环烷的联芳基结构的通用反应。

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