...
首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Indazolium halides as efficient ligands for Pd-catalyzed Suzuki-Miyaura cross-coupling of aryl bromides with arylboronic acids
【24h】

Indazolium halides as efficient ligands for Pd-catalyzed Suzuki-Miyaura cross-coupling of aryl bromides with arylboronic acids

机译:吲哚鎓卤化物是钯催化芳基溴化物与芳基硼酸的Suzuki-Miyaura交叉偶联的有效配体

获取原文
获取原文并翻译 | 示例
           

摘要

The indazolium halides containing various N-substituents have been conveniently prepared and applied in the palladium-catalyzed Suzuki-Miyaura cross-coupling reactions of aryl bromides with arylboronic acids at mild reaction conditions. The cross-coupling reaction provides the desired products in good to high yields. The ease of synthesis and the modularity, and the broad range of aryl bromides and arylboronic acids make this type of ligand attractive and promising for transition metal catalysis. (C) 2016 Elsevier Ltd. All rights reserved.
机译:含有各种N取代基的in唑鎓卤化物已经方便地制备,并用于在温和的反应条件下,钯催化的Suzuki-Miyaura芳基溴与芳基硼酸的交叉偶联反应。交叉偶联反应以高至高收率提供所需产物。易于合成和模块化,以及范围广泛的芳基溴化物和芳基硼​​酸,使得这种类型的配体具有吸引力,并有望用于过渡金属催化。 (C)2016 Elsevier Ltd.保留所有权利。

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