首页> 外文期刊>Organic & biomolecular chemistry >Binaphthyl-based chiral bifunctional organocatalysts for water mediated asymmetric List-Lerner-Barbas aldol reactions
【24h】

Binaphthyl-based chiral bifunctional organocatalysts for water mediated asymmetric List-Lerner-Barbas aldol reactions

机译:用于水介导的不对称List-Lerner-Barbas aldol反应的基于联萘基的手性双功能有机催化剂

获取原文
获取原文并翻译 | 示例
           

摘要

Novel binaphthyl-based chiral bifunctional organocatalysts were designed, synthesized and successfully applied to the asymmetric List-Lerner-Barbas aldol reaction in the presence of water. These organocatalysts were found to be effective catalysts for the reactions of symmetrical, unsymmetrical and cyclic ketones with different aldehydes to give the corresponding aldol products with higher yields (up to 98%) and very good ee's up to 99%. The catalytic system leads to higher yields and selectivities than the previously reported well-known proline based organocatalysts. In addition to the effect of solvent, additives, catalyst concentration, temperature and the substrate scope of the reactions were also investigated.
机译:设计,合成了新型的基于联萘基的手性双官能有机催化剂,并成功地将其用于在水存在下的不对称List-Lerner-Barbas aldol反应。发现这些有机催化剂对于对称,不对称和环状酮与不同醛的反应是有效的催化剂,从而以更高的产率(高达98%)和非常好的ee高达99%给出相应的羟醛产物。与先前报道的众所周知的基于脯氨酸的有机催化剂相比,该催化系统导致更高的产率和选择性。除了溶剂的影响外,还研究了添加剂,催化剂浓度,温度和反应的底物范围。

著录项

  • 来源
    《Organic & biomolecular chemistry》 |2016年第38期|9021-9032|共12页
  • 作者单位

    Supramolecular and Organometallic Chemistry Lab, School of Chemistry, Madurai Kamaraj University, Madurai-625 021, Tamil Nadu, India;

    Supramolecular and Organometallic Chemistry Lab, School of Chemistry, Madurai Kamaraj University, Madurai-625 021, Tamil Nadu, India;

    Supramolecular and Organometallic Chemistry Lab, School of Chemistry, Madurai Kamaraj University, Madurai-625 021, Tamil Nadu, India;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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