首页> 外文期刊>Advanced synthesis & catalysis >Synthesis of 2,4- and 2,5-Disubstituted Oxazoles via Metal-Catalyzed Gross-Coupling Reactions
【24h】

Synthesis of 2,4- and 2,5-Disubstituted Oxazoles via Metal-Catalyzed Gross-Coupling Reactions

机译:通过金属催化的总偶联反应合成2,4-和2,5-二取代的恶唑

获取原文
获取原文并翻译 | 示例
           

摘要

The rapid synthesis of 2,4- and 2,5-disub-stituted oxazoles via metal-catalyzed cross-coupling reactions is reported. The 4- or 5-position of the corresponding 4- or 5-halogenated 2-butylthiooxa-zoles was successfully functionalized via Suzuki-Miyaura, Sonogashira and Stille cross-coupling reactions. The 2-position of the 2-butylthiooxazoles obtained was further coupled to various organozinc reagents through palladium- or nickel-mediated cross-coupling reactions.
机译:据报道,通过金属催化的交叉偶联反应可以快速合成2,4-和2,5-二取代的恶唑。通过Suzuki-Miyaura,Sonogashira和Stille交叉偶联反应成功地官能化了相应的4-或5-卤代2-丁基硫代恶唑的4-或5-位。通过钯或镍介导的交叉偶联反应,将获得的2-丁基硫代恶唑的2-位进一步偶联至各种有机锌试剂。

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