期刊文献+

Ni催化Suzuki反应的研究进展 被引量:5

Progress of Ni-catalyzed Suzuki reaction
下载PDF
导出
摘要 综述了近年来镍催化的Suzuki偶联反应的研究进展。回顾了各类卤代芳香烃、磺酸芳基酯、有机硼等底物参与的Suzuki反应在反应条件方面的改进,随着催化剂、配体、还原剂的活性提高,反应条件越来越温和。比较了镍催化剂与钯催化剂的催化能力,镍催化剂向着稳定、高效、价廉的方向发展,且比钯催化剂适用范围广,是钯催化剂的理想替代品。介绍了新型的含氮杂环卡宾及非均相镍催化剂的发展现状及其特点。 The progress of Ni-catalyzed Suzuki cross-coupling reaction is reviewed. For all kinds of haloarenes, arene sulfonates and organoborates, with the enhancement of the activity catalyst, ligand and reducing agent, the reaction conditions become milder. The catalytic capacities of Pd catalyst and Ni catalyst are compared, and Ni catalyst is found to become more stable, effective and cheap. Furthermore, Ni catalyst can catalyze more substrates, hence, it is an ideal substitute of Pd catalyst. Lastly, the development of Ni catalyst of heterocyclic carbenes, heterogeneous catalyst and their advantages are summarized.
出处 《化工进展》 EI CAS CSCD 北大核心 2007年第5期615-623,共9页 Chemical Industry and Engineering Progress
关键词 催化剂 SUZUKI反应 Ni catalyst Suzuki cross-coupling reaction
  • 相关文献

参考文献57

  • 1Miyaura N,Yanagi T,Suzuki A.The palladium-catalyzed cross-coupling reaction of phenylboronic acid with haloarenes in the presence of bases[J].Synth.Commun.,1981,11(7):513-519.
  • 2Miyaura N,Suzuki A.Palladium-catalyzed cross-coupling reactions of organoboron compounds[J].Chem.Rev.,1995,95(7):2457-2483.
  • 3Suzuki A.Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles[J].J.Organomet.Chem.,1995-1998,1999,576:147-168.
  • 4Kotha S,Lahiri K,Kashinath D.Recent applications of the suzuki-miyaura cross-coupling reaction in organic synthesis[J].Tetrahedron,2002,58:9633-9695.
  • 5Hassan J,Sevignon M,Gozzi C,et al.Aryl-aryl bond formation one century after the discovery of the ullmann reaction[J].Chem.Rev.,2002,102(5):1359-1469.
  • 6Percec V,Bae J Y,Hill D H.Aryl mesylates in metal catalyzed homocoupling and cross-coupling reactions.2.suzuki-type nickel-catalyzed cross-coupling of aryl arenesulfonates and aryl mesylates with arylboronic acids[J].J.Org.Chem.,1995,60(4):1060-1065.
  • 7Saito S,Sakai M,Miyaura N.A synthesis of biaryls via nickel[0]-catalyzed cross-coupling reaction of chloroarenes with phenylboronic acids[J].Tetrahedron Lett.,1996,37(17):2993-2996.
  • 8Tang Z Y,Hu Q S.Triphenylphosphine as a ligand for room-temperature Ni(0)-catalyzed cross-coupling reactions of aryl chlorides with arylboronic acids[J].J.Org.Chem.,2006,71(5):2167-2169.
  • 9Saito S,Saori Oh-tani,Miyaura N.Synthesis of biaryls via a nickel(0)-catalyzed cross-coupling reaction of chloroarenes with arylboronic acids[J].J.Org.Chem.,1997,62(23):8024-8030.
  • 10Indolese A F.Suzuki-type coupling of chloroarenes with arylboronic acids catalysts by nickel compounds[J].Tetrahedron Lett.,1997,38(20):3513-3516.

二级参考文献3

共引文献8

同被引文献24

引证文献5

二级引证文献15

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部