...
首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >NEW PREPARATION OF TRIDENTATE BIS-OXAZOLINE CARBAZOLE LIGAND EFFECTIVE FOR ENANTIOSELECTIVE NOZAKI-HIYAMA REACTION
【24h】

NEW PREPARATION OF TRIDENTATE BIS-OXAZOLINE CARBAZOLE LIGAND EFFECTIVE FOR ENANTIOSELECTIVE NOZAKI-HIYAMA REACTION

机译:对映体选择性Nizaki-Hyyama反应的三苯甲基双-恶唑啉咔唑配体的新制备

获取原文
获取原文并翻译 | 示例

摘要

A new preparation of the tridentate bis-oxazoline carbazole ligand 1 is described.This method features direct formation of the amide,which is a precursor of the ligand 1,via the Pd-catalyzed amidation and following BF3·OEt2 mediated oxazoline formation.This method required only 2 steps from the aryl iodide to form the bis-oxazoline ligand;hence,it would be generally used for preparing other bis-oxazoline ligands.
机译:描述了一种新的三齿双恶唑啉咔唑配体1的制备方法。该方法的特点是通过Pd催化的酰胺化反应,并在BF3·OEt2介导的恶唑啉形成后直接形成酰胺,它是配体1的前体。从芳基碘化物仅需两个步骤即可形成双恶唑啉配体;因此,通常用于制备其他双恶唑啉配体。

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