首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Tandem Aza-Michael–Aldol Reactions: One-Pot Synthesis of Functionalized Piperidine Derivatives
【24h】

Tandem Aza-Michael–Aldol Reactions: One-Pot Synthesis of Functionalized Piperidine Derivatives

机译:串联Aza-Michael-Aldol反应:一锅合成功能化哌啶衍生物

获取原文
获取原文并翻译 | 示例
           

摘要

A series of novel functionalized piperidine derivatives were conveniently prepared by three-component tandem aza-Michael–Aldol reactions of α,β-unsaturated enones with substituted sulfonamides in the presence of DBU. The structures of the compounds synthesized were characterized by spectral data and X-ray crystal diffraction.
机译:在DBU存在下,通过α,β-不饱和烯酮的三组分串联aza-Michael-Aldol反应与取代的磺酰胺方便地制备了一系列新颖的官能化哌啶衍生物。合成的化合物的结构通过光谱数据和X射线晶体衍射表征。

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