Markovnikov selective hydroaminocarbonylation of alkenes over a porous monophoshine polymer supported palladium catalyst
文献类型：期刊论文
| 作者 | Li,Jiajun; Zhao,Kang; Cui,Xinjiang ; Wang,Lailai; Shi,Feng
|
| 刊名 | Catalysis Science & Technology
 |
| 出版日期 | 2024 |
| 卷号 | 14期号:17页码:4848-4853 |
| DOI | 10.1039/d4cy00742e |
| 英文摘要 | Here we develop a porous monophoshine polymer supported Pd catalyst (Pd/POL-m-3vPPh3) for hydroaminocarbonylation of aromatic alkenes with amines, showing excellent catalytic activity (up to 97% yield) and Markovnikov selectivity (up to 99%) for producing branched amides. This catalyst exhibits broad substrate compatibility, and is reused for two times with no significant decline in the performance and three times with no significant Pd leaching, as well as applied for the synthesis of naproxen. |
| 语种 | 英语 |
| 源URL | [http://ir.licp.cn/handle/362003/30722]  |
| 专题 | 兰州化学物理研究所_OSSO国家重点实验室 |
| 通讯作者 | Wang,Lailai; Shi,Feng |
| 作者单位 | 1.Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences 2.1.Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences，2.University of Chinese Academy of Sciences 3.Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences 4.Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences 5.Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences |
| 推荐引用方式 GB/T 7714 | Li,Jiajun,Zhao,Kang,Cui,Xinjiang,et al. Markovnikov selective hydroaminocarbonylation of alkenes over a porous monophoshine polymer supported palladium catalyst[J]. Catalysis Science & Technology,2024,14(17):4848-4853. |
| APA | Li,Jiajun,Zhao,Kang,Cui,Xinjiang,Wang,Lailai,&Shi,Feng.(2024).Markovnikov selective hydroaminocarbonylation of alkenes over a porous monophoshine polymer supported palladium catalyst.Catalysis Science & Technology,14(17),4848-4853. |
| MLA | Li,Jiajun,et al."Markovnikov selective hydroaminocarbonylation of alkenes over a porous monophoshine polymer supported palladium catalyst".Catalysis Science & Technology 14.17(2024):4848-4853. |
入库方式： OAI收割
来源：兰州化学物理研究所
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