首页> 外文期刊>Chemistry: A European journal >Direct Introduction of a Dimesitylboryl Group Using Base-Mediated Substitution of Aryl Halides with Silyldimesitylborane
【24h】

Direct Introduction of a Dimesitylboryl Group Using Base-Mediated Substitution of Aryl Halides with Silyldimesitylborane

机译:直接使用芳基卤化物与甲硅烷基二甲硅烷基硼烷的取代基直接引入二甲磺基基团

获取原文
获取原文并翻译 | 示例
           

摘要

The first dimesitylboryl substitution of aryl halides with a silylborane bearing a dimesitylboryl group in the presence of alkali-metal alkoxides is described. The reactions of aryl bromides or iodides with Ph2MeSi-BMes(2) and Na(OtBu) afforded the desired aryl dimesitylboranes in good to high yields and with high borylation/silylation ratios. Selective reaction of the sterically less-hindered C-Br bond of dibromoarenes provided monoborylated products. This reaction was used to rapidly construct a D-pi-A aryl dimesityl borane with a non-symmetrical biphenyl spacer.
机译:描述了在碱金属醇盐存在下用带有二甲基异丁烯基的甲硅烷基硼烷对芳基卤化物的第一次二甲基异丁烯基取代。芳基溴化物或碘化物与Ph2MeSi-BMes(2)和Na(OtBu)的反应以高到高的收率和高的硼化/甲硅烷基化比提供了所需的芳基二聚三聚戊二烯。二溴芳烃在空间上受阻较小的C-Br键的选择性反应提供了单硼化产物。该反应用于快速构建具有非对称联苯间隔基的D-pi-A芳基二甲硅烷基硼烷。

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