...
首页> 外文期刊>Chemistry of heterocyclic compounds >Benzyl-4,5-dihydroisoxazoles from benzylcyclo-propanes: Regioselective insertion of an n=o fragment into the three-membered carbocycle of benzylcyclopropanes by the action of nitrous acid
【24h】

Benzyl-4,5-dihydroisoxazoles from benzylcyclo-propanes: Regioselective insertion of an n=o fragment into the three-membered carbocycle of benzylcyclopropanes by the action of nitrous acid

机译:来自苄基环素 - 丙烷的苄基-4,5-二羟基异恶唑:通过亚硝酸的作用,将n = o片段的区域插入苄基环丙烷的三元碳循环中

获取原文
获取原文并翻译 | 示例
           

摘要

The action of equimolar amounts of nitrous acid formed in situ on benzylcyclopropanes with electron-donor and electron-withdrawing substituents in the aromatic part of the substrate lead, at certain temperatures, exclusively to the insertion of an N=O fragment into the three-membered carbocycle with subsequent formation of a heterocyclic isoxazoline (4,5-dihydroisoxazole) system.
机译:在某些温度下,在苄基环丙烷原位对苄基环丙烷在苄基环丙烷上形成的亚苄酸与电子 - 供给芳族铅中的芳香部分中的取代基,专门用于将n = o片段插入三个元素 碳纤维随后形成杂环异恶唑啉(4,5-二羟基异恶唑)体系。

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