研究论文

铁催化的N-芳基四氢异喹啉α-sp3-C—H键在空气中的氧化磷酸化

  • 张艳 ,
  • 罗莎 ,
  • 冯柏年
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  • 江南大学药学院 无锡 214122

收稿日期: 2014-08-21

  修回日期: 2014-09-28

  网络出版日期: 2014-10-09

基金资助

国家自然科学基金(No.21302067)和江苏省自然科学基金(No.BK20130120)资助项目.

Iron-Catalyzed Oxidative Phosphonation of α-sp3-C—H Bonds of N-Aryl Tetrahydroisoquinolines with Air as Oxidant

  • Zhang Yan ,
  • Luo Sha ,
  • Feng Bainian
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  • School of Pharmaceutical Science, Jiangnan University, Wuxi 214122

Received date: 2014-08-21

  Revised date: 2014-09-28

  Online published: 2014-10-09

Supported by

Project supported by the National Natural Science Foundation of China (No.21302067) and the National Natural Science Foundation of Jiangsu Province (No.BK20130120).

摘要

以FeCl3作为催化剂, 空气作为氧化剂, 在温和的条件下实现了叔胺氮的邻位碳原子上sp3-C—H键与亚磷酸二烷基酯、二芳基磷氧化合物的H—P键的交叉脱氢偶联. 安全、方便、环境友好、高效地合成了一系列具有重要生物活性α-氨基磷酸酯化合物.

本文引用格式

张艳 , 罗莎 , 冯柏年 . 铁催化的N-芳基四氢异喹啉α-sp3-C—H键在空气中的氧化磷酸化[J]. 有机化学, 2014 , 34(11) : 2249 -2254 . DOI: 10.6023/cjoc201408025

Abstract

An efficient cross-dehydrogenative-coupling (CDC) between sp3-C—H bond adjacent to a nitrogen atom of tertiary amine and H—P bonds of dialkyl phosphites and diaryl phosphate was developed using FeCl3 as catalyst and air as oxidant under mild reaction conditions. The safe, convenient, environmental and efficiently benign to synthesize a series of biologically important α-aminophosphonates.

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