...
首页> 外文期刊>Organic letters >Br?nsted Acid Accelerated Pd-Catalyzed Direct Asymmetric Allylic Alkylation of Azlactones with Simple Allylic Alcohols:A Practical Access to Quaternary Allylic Amino Acid Derivatives
【24h】

Br?nsted Acid Accelerated Pd-Catalyzed Direct Asymmetric Allylic Alkylation of Azlactones with Simple Allylic Alcohols:A Practical Access to Quaternary Allylic Amino Acid Derivatives

机译:布朗斯台德酸促进的Pd催化的内酯与简单烯丙基醇直接不对称烯丙基烷基化:季铵烯丙基氨基酸衍生物的实用途径

获取原文
获取原文并翻译 | 示例
           

摘要

A Br?nsted acid accelerated Pd-catalyzed asymmetric allylic alkylation of azlactones with simple allylic alcohols under mild reaction conditions has been realized, which provides a direct and readily scalable approach for the synthesis of allcarbon quaternary allylic amino acid derivatives in excellent yields and good enantioselectivities.
机译:已经实现了布朗斯台德酸在温和的反应条件下与简单的烯丙基醇促进的Pd催化的内酯的Pd催化的不对称烯丙基烷基化反应,这为直接合成,易于扩展的全碳季铵基氨基酸衍生物的合成提供了直接且易于扩展的方法,具有优异的收率和良好的对映选择性。

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