...
首页> 外文期刊>Angewandte Chemie >LiCl-Mediated Preparation of Functionalized Benzylic Indium(III)Halides and Highly Chemoselective Palladium-Catalyzed Cross-Coupling in a Protic Cosolvent
【24h】

LiCl-Mediated Preparation of Functionalized Benzylic Indium(III)Halides and Highly Chemoselective Palladium-Catalyzed Cross-Coupling in a Protic Cosolvent

机译:LiCl介导的功能化苯甲酸铟(III)卤化物与质子助溶剂中高度化学选择性钯催化的交叉偶联反应的制备

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The development of palladium-catalyzed cross-coupling reactions has revolutionized the formation of carbon-carbon bonds.These coupling reactions have found many applications in natural product synthesis,material science,and medicinal chemistry.The Suzuki reaction,which involves organoboron compounds,has been widely used because of the ready availability of boronic esters and their excellent compatibility with many functional groups during the cross-coupling reaction.Typically,functional groups bearing acidic protons,ketones,and aldehydes are compatible with these coupling reactions.However,the low reactivity of boronic acids may require harsh reaction conditions or sophisticated ligand systems.Furthermore,some classes of boronic acid derivatives such as functionalized benzylic boronic acids are more difficult to prepare.
机译:钯催化交叉偶联反应的发展彻底改变了碳-碳键的形成。这些偶联反应已在天然产物合成,材料科学和药物化学中得到了许多应用。涉及有机硼化合物的Suzuki反应已得到广泛应用。由于硼酸酯的易得性及其在交叉偶联反应中与许多官能团的优异相容性而被广泛使用。通常,带有酸性质子,酮和醛的官能团与这些偶联反应相容。硼酸可能需要苛刻的反应条件或复杂的配体体系。此外,某些类型的硼酸衍生物(例如官能化的苄基硼酸)更难以制备。

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