期刊文献+

Suzuki偶联反应催化剂及其作用机理研究进展 被引量:3

Research Progress of Suzuki Cross-Coupling Reaction Catalyst and Its Action Mechanism
下载PDF
导出
摘要 Suzuki偶联反应,是指在温和条件下,卤代苯与苯硼酸类化合物经钯催化剂作用发生交叉偶联,生成新C-C键的反应,其在药物研发与合成中具有重要的应用.钯基催化剂是Suzuki偶联反应的关键,开发低成本、新型高活性催化剂并探究其作用机理对于该反应的广泛应用具有重要意义.通过对钯基催化剂种类、应用范围及其可能的催化机理相关研究进行的分析,可为设计新型Suzuki偶联反应的钯基纳米催化剂提供有效信息. Suzuki cross-coupling refers to the reaction,in which halobenzene and benzenic boric acid are catalyzed by palladium catalyst to generate a new C-C bond under mild conditions.Suzuki cross-coupling reaction plays a key role in drug development and synthesis.With palladium-based catalyst being the key factor of Suzuki coupling reaction,it is of great significance to develop a new type of catalyst with low cost and high activity,as well as to explore its catalytic mechanism.The aim of this paper is to review the types,application ranges and possible catalytic mechanism of palladium catalysts,which is helpful for the design of novel palladium-based nano-catalysts for Suzuki coupling reaction.
作者 胡建平 严潇 罗亚飞 梁立 甘亚 刘嵬 谢涛 吴志祥 唐典勇 HU Jianping;YAN Xiao;LUO Yafei;LIANG Li;GAN Ya;LIU Wei;XIE Tao;WU Zhixiang;TANG Dianyong(School of Pharmacy and Bioengineering,Chengdu University,Chengdu 610106,China;Sichuan Industrial Institute of Antibiotics,Chengdu University,Chengdu 610052,China;Collaborative Innovation Center of Targeted Therapeutics and Innovation, Chongqing University of Arts and Sciences,Chongqing 402160,China)
出处 《成都大学学报(自然科学版)》 2019年第2期115-123,共9页 Journal of Chengdu University(Natural Science Edition)
基金 国家自然科学基金(11247018、31870655) 四川省教育厅重点科研计划(17ZA0194)资助项目
关键词 SUZUKI偶联反应 钯基催化剂 反应机理 催化剂设计 Suzuki cross coupling reaction palladium-based catalyst reaction mechanism catalyst design
  • 相关文献

参考文献4

二级参考文献60

  • 1FEUERSTEIN M,LAURENTI D, BOUGEANT C, et al.Palladium tetraphosphine catalysed cross coupling of aryl bromides with arylboronic acids:remarkable influence of the nature of the ligand [ J ].Chemical Communications,2001,325N326.
  • 2FEUERSTEIN M, DOUCET H, STANTELLI M.Tetraphosphine/ palladium-catalysed Suzuki cross-coupling with sterically hin- dered aryl bromides and arylboronic acids [J].Tetrahedron Let- ters,2001,42:6667~6670.
  • 3FEUERSTEIN M, DOUCET H, STANTELLI M.Efficient coupling of heteroaryl bromides with arylboronic acids in the presence of a palladium tetraphosphine catalyst [J].Tetrahedron Letters,2001, 42:5659~5662.
  • 4FEUERSTEIN M, DOUCET H, SANTELLI M.Palladium eataly sed cross-coupling of aryl chlorides with arylboronic acids in the presence of a newtetraphosphine ligand[J].Synlett,2001, 1458.
  • 5ARDUENGO A J, HARLOW R L, KINE M.A stable crystalline carbine[J ].Journal of the American Chemical Society,1991,113. 361~363.
  • 6HERRMANN W A, REIS1NGER C P, SPIEGLER M.Chelating N-heterocyclic carbene ligands in palladium-catalyzed heck- type reactions [ J ].Journal of Organometal|ic Chemistry, 1998,557:93~96.
  • 7BOHM V P W, CSTOTFMAYR C W K, HERRMANN W A, et al.N-Heterocyclic carbene complexes of palladium(0): synthesis and application in the Suzuki cross-coupling reaction[J].Jour- nal of Organometallic Chemistry,2000,595:186~190.
  • 8HERRMANN W A , GSTOTFMAYER C W K, BOHM V P W, et al.A defined N-heterocyclic carbene Complex for the palladi- um-catalyzed suzuki cross-couplingof aryl chlorides at ambient temperatures[J].Angewandte Chemie International Edition,2002, 41:1363-1365.
  • 9ARENTSEN K, CADD1CK S, CLOKE G N, et al.Suzuki Miyau- ra cross-coupling of aryl and alkyl halides using palladium/imi- dazolium salt protocols[J].Tetrahedron Letters,2004,45:3511 ~ 3515.
  • 10MARION N, NAVARRO O, NOLAN S P, et al.Modified (NHC) Pd (allyl)Cl (NHC =N-Heterocyclic Carbene) complexes forroom-temperature Suzuki-Miyaura and Buchwald-Hartwig Re- actionslJ l.Journal of the American Chemical Society,2006,128: 4101-4111.

共引文献25

同被引文献8

引证文献3

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