首页> 外文期刊>European journal of organic chemistry >Highly enantioselective henry reaction catalyzed by C_2-symmetric modular BINOL-oxazoline Schiff base copper(II) complexes generated in situ
【24h】

Highly enantioselective henry reaction catalyzed by C_2-symmetric modular BINOL-oxazoline Schiff base copper(II) complexes generated in situ

机译:原位生成的C_2对称模块化BINOL-恶唑啉席夫碱铜(II)配合物催化高度对映亨利反应

获取原文
获取原文并翻译 | 示例
           

摘要

A 16-member library of C_2-symmetric modular chiral BINOL-oxazoline Schiff base copper(II) complex catalysts generated in situ was easily generated in a one-pot, three-component manner. This approach avoided the need for isolation and characterization of ligands and greatly improved the catalyst screening efficiency. This modular catalyst library was evaluated in the asymmetric Henry reaction, for which good yields (up to 98%) and good to excellent enantioselectivities (up to 98% ee) were obtained under mild conditions. A new modular library of C_2-symmetric chiral BINOL-oxazoline Schiff base copper(II) complex catalysts was generated in situ in a one-pot, three-component manner. This library greatly improves catalystscreening efficiency and was used in the asymmetric Henry reaction, for which good yields and good to excellent enantioselectivities were obtained under mild conditions.
机译:原位生成的C_2对称模块化手性BINOL-恶唑啉席夫碱铜(II)络合物的16元文库很容易以一锅,三组分的方式生成。该方法避免了分离和表征配体的需要,并大大提高了催化剂的筛选效率。在不对称亨利反应中评估了该模块化催化剂库,在温和条件下可获得良好的收率(高达98%)和良好的对映选择性(高达98%ee)。以一锅,三组分的方式原位生成了新的C_2-对称手性BINOL-恶唑啉席夫碱铜(II)配合物模块库。该文库极大地提高了催化剂的筛选效率,并用于不对称的亨利反应中,在温和条件下可获得良好的收率和良好至优异的对映选择性。

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