Amide as an efficient ligand in the palladium-catalyzed Suzuki coupling reaction in water/ethanol under aerobic conditions

Hai Yang Liu Kun Wang Hai Yan Fu Mao Lin Yuan Hua Chen Rui Xiang Li

引用本文: Hai Yang Liu,  Kun Wang,  Hai Yan Fu,  Mao Lin Yuan,  Hua Chen,  Rui Xiang Li. Amide as an efficient ligand in the palladium-catalyzed Suzuki coupling reaction in water/ethanol under aerobic conditions[J]. Chinese Chemical Letters, 2011, 22(6): 738-740. doi: 10.1016/j.cclet.2010.12.048 shu
Citation:  Hai Yang Liu,  Kun Wang,  Hai Yan Fu,  Mao Lin Yuan,  Hua Chen,  Rui Xiang Li. Amide as an efficient ligand in the palladium-catalyzed Suzuki coupling reaction in water/ethanol under aerobic conditions[J]. Chinese Chemical Letters, 2011, 22(6): 738-740. doi: 10.1016/j.cclet.2010.12.048 shu

Amide as an efficient ligand in the palladium-catalyzed Suzuki coupling reaction in water/ethanol under aerobic conditions

摘要: Amide, which is derived from proline and is inexpensive and air-stable, has been synthesized and characterized by 1H NMR,13C NMR, and MS.It was found to be an efficient ligand in the palladium-catalyzed Suzuki cross-coupling reaction.In the Pd/amide catalytic system, aryl bromides can be coupled with phenylboronic acid in ethanol/water(1:2;v/v)in excellent yields even with a low Pd loading of 0.01 mol%.Moreover, the scope of the reaction is broad, and a wide variety of functional groups are tolerant.

English

  • 加载中
计量
  • PDF下载量:  2
  • 文章访问数:  1570
  • HTML全文浏览量:  40
文章相关
  • 收稿日期:  2010-10-15
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

/

返回文章