首页> 外文OA文献 >Highly Diastereo- and Enantioselective Michael Additions of 3-Substituted Oxindoles to Maleimides Catalyzed by Chiral Bifunctional Thiourea-Tertiary Amine
【2h】

Highly Diastereo- and Enantioselective Michael Additions of 3-Substituted Oxindoles to Maleimides Catalyzed by Chiral Bifunctional Thiourea-Tertiary Amine

机译:手性双官能硫脲-叔胺催化3-取代的吲哚向马来酰亚胺的高度非对映和对映选择性迈克尔加成反应

摘要

A highly diastereo- and enantioselective Michael addition reaction with respect to prochiral 3-substituted oxindoles and maleimides by a chiral bifunctional thiourea tertiary amine catalyst was investigated for the first time. The corresponding adducts, containing a quaternary center at the C3-position of the oxindole as well as a vicinal tertiary center, were generally obtained in good to high yields (up to 92%) with high to excellent diastereo- (up to 99:1 dr) and enantioselectivities (up to 99% ee).
机译:首次研究了手性双官能硫脲叔胺催化剂对前手性3-取代的羟吲哚和马来酰亚胺的高度非对映选择性和对映选择性迈克尔加成反应。相应的加合物通常在高至高收率(最高92%)和高至极好非对映体(最高99:1)的条件下获得,这些加合物在羟吲哚的C3位上具有一个四级中心以及一个邻级三级中心。 dr)和对映选择性(最高99%ee)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利

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