...
首页> 外文期刊>Bulletin of the Korean Chemical Society >Synthesis of Imidazo[1,5-a]quinolines and Imidazo[5,1-a]isoquinolines via the In-Mediated Allylation of Reissert Compounds
【24h】

Synthesis of Imidazo[1,5-a]quinolines and Imidazo[5,1-a]isoquinolines via the In-Mediated Allylation of Reissert Compounds

机译:通过介导的Reissert化合物烯丙基化合成咪唑并[1,5-a]喹啉和咪唑并[5,1-a]异喹啉

获取原文
获取原文并翻译 | 示例
           

摘要

Allylindium reagents have been used extensively for the introduction of allyl group in a Barbier type manner to various electrophiles.Although many reactive electrophiles such as aldehydes and imines have been used in the indium-mediated allylations, the reaction of less reactive nitrile has not been reported much except the first successful results of Yamamoto group and our recent papers.
机译:烯丙基化试剂已被广泛用于以Barbier型方式将烯丙基引入各种亲电子试剂中。尽管许多反应性亲电试剂(如醛和亚胺)已用于铟介导的烯丙基化反应中,但尚未报道反应性较低的腈的反应。除了Yamamoto集团的第一个成功成果和我们最近的论文。

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