...
首页> 外文期刊>Journal of Fluorine Chemistry >A new tetrasubstituted alpha-fluoro cyclohexanone bearing a fluoroisopropyl group at C5
【24h】

A new tetrasubstituted alpha-fluoro cyclohexanone bearing a fluoroisopropyl group at C5

机译:一种新的四取代的α-氟环己酮,在C5处带有氟异丙基

获取原文
获取原文并翻译 | 示例
           

摘要

A new tetrasubstituted cyclohexanone 5 fluorinated at C2 and having a fluoroisopropyl group at C5 has been synthesized in five steps from 3-methyl cyclohexenone and the structure of both diastereomers fully assigned.It is shown that diastereomer Ia having the fluorine atom at C2 in the axial position (in the most populated conformer of this diastereomer) is major and is a good catalyst for epoxidation of trans-olefins by oxone while diastereomer IIe is not.Moreover,only 0.3 equiv.of 5-Ia are necessary and the ketone is totaly recovered after reaction (no Baeyer-Villiger).
机译:从3-甲基环己烯酮分五个步骤合成了在C2处氟化并在C5处具有氟异丙基的新的四取代环己酮5,表明两种非对映异构体Ia的轴向均在C2处具有氟原子。位置(在该非对映异构体的最稠密构象异构体中)是主要的,并且是氧杂环丁烷反式烯烃环氧化的良好催化剂,而非对映异构体IIe则是必要的。此外,仅0.3当量的5-Ia是必需的,并且可以完全回收酮反应后(无Baeyer-Villiger)。

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