...
首页> 外文期刊>Organic letters >Highly Regio- and Stereoselective Synthesis of Boron-Substituted Enynes via Copper-Catalyzed Borylation of Conjugated Diynes
【24h】

Highly Regio- and Stereoselective Synthesis of Boron-Substituted Enynes via Copper-Catalyzed Borylation of Conjugated Diynes

机译:通过共轭二炔的铜催化硼化反应高度取代硼和立体选择性的硼取代烯

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

A mild copper-catalyzed regio- and stereoselective monoborylation of conjugated diynes with bis(pinacolato)diboron that affords enynylboronates is reported. The reaction is efficient for different types of conjugated diynes including unsymmetrical diynes and produces enynylboron compounds with high and complementary regioselectivity compared with classical hydrometalation reactions. In particular, the reactions of internal conjugated diynes with a silyl substitution produced highly functionalized enynes with high regio- and stereoselectivity, which can be used in further transformations.
机译:据报道,轻度的铜催化的共轭二炔与双(频哪醇)二硼的区域选择性和立体选择性的单硼化,可以提供烯丙基硼酸酯。该反应对于包括不对称二炔在内的不同类型的共轭二炔有效,并且与传统的加氢金属化反应相比,生成的烯丙基硼化合物具有高和互补的区域选择性。特别地,内部共轭二炔与甲硅烷基取代的反应产生具有高区域选择性和立体选择性的高度官能化的烯炔,其可用于进一步的转化中。

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