...
首页> 外文期刊>Catalysis Communications >Enantioselective cross dehydrogenative coupling reaction catalyzed by Rose Bengal incorporated-Cu(I)-dimeric chiral complexes
【24h】

Enantioselective cross dehydrogenative coupling reaction catalyzed by Rose Bengal incorporated-Cu(I)-dimeric chiral complexes

机译:玫瑰孟加拉掺入-Cu(I) - 二二甲基综合催化催化催化催化的致注色的交叉脱氢偶联反应

获取原文
获取原文并翻译 | 示例
           

摘要

A novel dimeric chiral Cu(I) amino alcohol based in-situ generated catalyst in combination with Rose Bengal as a photo-redox catalyst were used for the first time for asymmetric cross dehydrogenative coupling of N-aryl tetrahydroisoquinoline with terminal alkynes enroute for propargylic amines synthesis using molecular oxygen as a terminal oxidant. This methodology provides an atom economical and green way to access diversified optically active alkynylation product selectively at Cl-position of N-aryl tetrahydroisoquinoline under moderate conditions with high enantioselectivity (up to 99%) and excellent yield (up to 90%).
机译:首次将一种新型的二聚手性铜(I)氨基醇原位生成催化剂与作为光氧化还原催化剂的孟加拉玫瑰相结合,用于N-芳基四氢异喹啉与末端炔烃的不对称交叉脱氢偶联,以分子氧为末端氧化剂合成丙炔胺。该方法提供了一种原子经济的绿色方法,在温和条件下,在N-芳基四氢异喹啉的Cl位置选择性地获得多种光学活性炔化产物,具有高对映选择性(高达99%)和优异的产率(高达90%)。

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