首页> 外文期刊>Research on Chemical Intermediates >Formation of highly caged compounds through EMels-Alder cycloaddition of 3-bromo-7-(lbromomethyl)tetracyclo[5.3.1.0~(2,6).0~(4,8)]undeca-10(12)-ene-9,ll-dione with itself and with cyclopentadiene
【24h】

Formation of highly caged compounds through EMels-Alder cycloaddition of 3-bromo-7-(lbromomethyl)tetracyclo[5.3.1.0~(2,6).0~(4,8)]undeca-10(12)-ene-9,ll-dione with itself and with cyclopentadiene

机译:通过3-溴-7-(溴甲基)四环[5.3.1.0〜(2,6).0〜(4,8)] undeca-10(12)-ene-9的EMels-Alder环加成反应形成高笼状化合物,II-二酮本身与环戊二烯

获取原文
获取原文并翻译 | 示例
           

摘要

Diels-Alder reaction of the cage compound 2 with itself, leading to the highly caged compound 3, as well as with cyclopentadiene, leading to compounds 4 and 5, is described.
机译:描述了笼状化合物2与其自身的狄尔斯-阿尔德反应,导致高度笼蔽的化合物3,以及与环戊二烯的狄尔斯-阿尔德反应,导致化合物4和5。

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