...
首页> 外文期刊>Catalysis Letters >Palladium-Catalyzed Decarboxylative Csp(2)-Csp(2) Cross-Coupling Reactions: An Efficient Route for Synthesis of Azaisoflavone Derivatives
【24h】

Palladium-Catalyzed Decarboxylative Csp(2)-Csp(2) Cross-Coupling Reactions: An Efficient Route for Synthesis of Azaisoflavone Derivatives

机译:钯催化的脱羧Csp(2)-Csp(2)交叉偶联反应:合成氮杂黄酮衍生物的有效途径

获取原文
获取原文并翻译 | 示例
           

摘要

An efficient and step-economical ligand-free palladium-catalyzed decarboxylative functionalization of quinolinone-3-carboxylic acids has been well developed. Note that the reaction could proceed smoothly under an argon atmosphere at relatively low temperature by using Pd(OAc)(2) as the catalyst and Ag2CO3 as the oxidant. In this protocol, various functionalities were compatible under the reaction condition, and a series of biologically important azaisoflavone derivatives were obtained in moderate to high yields.
机译:喹啉酮-3-羧酸的有效且无步骤经济的无配体钯催化的脱羧官能化已经得到很好的发展。注意,通过使用Pd(OAc)(2)作为催化剂和Ag2CO3作为氧化剂,该反应可以在相对较低的氩气气氛下平稳进行。在该协议中,各种功能在反应条件下均兼容,并且以中等至高收率获得了一系列生物学上重要的氮杂异黄酮衍生物。

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