首页> 外文期刊>Chemical Communications >Tandem Nazarov cyclization-halovinylation of divinyl ketones under Vilsmeier conditions: synthesis of highly substituted cyclopentadienes
【24h】

Tandem Nazarov cyclization-halovinylation of divinyl ketones under Vilsmeier conditions: synthesis of highly substituted cyclopentadienes

机译:在维尔斯迈尔条件下串联纳扎罗夫二乙烯基酮的环化-卤代烷基化:高度取代的环戊二烯的合成

获取原文
获取原文并翻译 | 示例
       

摘要

A new Vilsmeier reagent-mediated Nazarov cyclization-halovinylation reaction of divinyl ketones was developed to provide a straightforward method for the synthesis of highly substituted cyclopentadienes with the advantages of simplicity of execution, readily available substrates, cheap reagents, and broad range of potential products and applications.
机译:开发了一种新的Vilsmeier试剂介导的二乙烯基酮的Nazarov环化-卤化反应,为合成高度取代的环戊二烯提供了一种简便易行的方法,其优点是操作简单,易于获得的底物,廉价的试剂以及广泛的潜在产品和应用程序。

著录项

  • 来源
    《Chemical Communications》 |2010年第13期|p.2247-2249|共3页
  • 作者单位

    Department of Chemistry, Northeast Normal University,Changchun 130024, China;

    Department of Chemistry, Northeast Normal University,Changchun 130024, China;

    Department of Chemistry, Northeast Normal University,Changchun 130024, China;

    Department of Chemistry, Northeast Normal University,Changchun 130024, China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 13:23:33

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