...
首页> 外文期刊>European journal of organic chemistry >An eco-friendly asymmetric organocatalytic conjugate addition of malonates to α,β-unsaturated aldehydes: Application on the synthesis of chiral indoles
【24h】

An eco-friendly asymmetric organocatalytic conjugate addition of malonates to α,β-unsaturated aldehydes: Application on the synthesis of chiral indoles

机译:丙二酸酯向α,β-不饱和醛的生态友好型不对称有机催化共轭加成:在手性吲哚合成中的应用

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The asymmetric Michael addition of malonates to α,β-unsaturated aldehydes using a modified J?rgensen-Hayashi organocatalyst in EtOH:brine solvent media is reported. The procedure proceeds smoothly to afford the corresponding Michael adducts in good yields with excellent enantioselectivities. The resulting Michael adducts represent excellent building blocks for the synthesis of chiral indoles. The asymmetric Michael reaction using a modified J?rgensen-Hayashi organocatalyst in EtOH:brine solvent media is reported. This procedure afforded the corresponding Michael adducts in good yields and with excellent enantioselectivities. The resulting adducts were further used as chiral building blocks for the synthesis of indoles.
机译:据报道,在EtOH:盐水溶剂介质中,使用改性的Jrrgensen-Hayashi有机催化剂将丙二酸酯不对称地添加到α,β-不饱和醛上。该过程顺利进行,以良好的对映选择性很好地提供了相应的迈克尔加合物。所得的迈克尔加合物代表了合成手性吲哚的极好基石。报道了在EtOH:盐水溶剂介质中使用改性的Jrrgensen-Hayashi有机催化剂进行的不对称迈克尔反应。该方法以良好的产率和优异的对映选择性提供了相应的迈克尔加合物。所得的加合物被进一步用作手性合成吲哚的结构单元。

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