...
首页> 外文期刊>Tetrahedron, Asymmetry: The International Journal for Repid Publication on all Aspects of Asymmetry in Orgainc, Inorganic, Organometallic, Physical and Bio-Organic Chemistry >N-allylation of anilides with chiral palladium catalysts: the first catalytic asymmetric synthesis of axially chiral anilides
【24h】

N-allylation of anilides with chiral palladium catalysts: the first catalytic asymmetric synthesis of axially chiral anilides

机译:用手性钯催化剂对苯甲酰胺进行N-烯丙基化:轴向手性苯甲酸酯的首次催化不对称合成

获取原文
获取原文并翻译 | 示例
           

摘要

The first catalytic asymmetric synthesis of axially chiral anilides has been carried out under palladium-catalyzed allylation reaction conditions with chiral phosphine ligands. Allylation of anilides bearing an ortho tert-butyl group with a palladium catalyst and (S)-BINAP as a chiral ligand gave axially chiral anilides in about 50% ee. (C) 2003 Elsevier Science Ltd. All rights reserved. [References: 20]
机译:在手性膦配体的钯催化的烯丙基化反应条件下,进行了轴向手性苯甲酸酯的首次催化不对称合成。用钯催化剂和(S)-BINAP作为手性配体对带有邻叔丁基的苯甲酸酯进行烯丙基化,得到轴向手性苯甲酸酯为约50%ee。 (C)2003 Elsevier ScienceLtd。保留所有权利。 [参考:20]

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