Unsymmetric-1,3-disubstituted imidazolium salt for palladium-catalyzed Suzuki-Miyaura cross-coupling reactions of aryl bromides
Yu, HW; Shi, JC; Zhang, H; Yang, PY; Wang, XP; Jin, ZL
刊名journal of molecular catalysis a-chemical
2006-05-02
卷号250期号:1-2页码:15-19
关键词palladium imidazol-2-ylidene Suzuki-Miyaura reaction aryl bromides catalysis
英文摘要a series of 1-(ferrocenylethyl)-3-substituted-imidazolium salts [3-substitute=2,6-di(iso-propyl)phenyl (1a), 2,4,6-trimethylphenyl (1b), tertbutyl (1c), i-ad (1d), cyclohexyl (1e)] have been synthesized from a racemic ferrocertylethyl acetate and the corresponding n-substituted imidazole in high yields (70-94%). a combination of pd(oac)(2) and 1a-d was found to form an excellent catalyst system for the suzuki-miyaura cross-coupling reactions of aryl bromides with phenylboronic acid in the presence of cs2co3 (c) 2006 elsevier b.v. all rights reserved.
WOS标题词science & technology ; physical sciences
类目[WOS]chemistry, physical
研究领域[WOS]chemistry
关键词[WOS]heterocyclic carbene ligands ; room-temperature ; chlorides ; complexes ; amination ; biaryls
收录类别SCI
语种英语
WOS记录号WOS:000237318000004
公开日期2015-11-17
内容类型期刊论文
源URL[http://159.226.238.44/handle/321008/140237]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
作者单位1.Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
2.Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116012, Peoples R China
推荐引用方式
GB/T 7714
Yu, HW,Shi, JC,Zhang, H,et al. Unsymmetric-1,3-disubstituted imidazolium salt for palladium-catalyzed Suzuki-Miyaura cross-coupling reactions of aryl bromides[J]. journal of molecular catalysis a-chemical,2006,250(1-2):15-19.
APA Yu, HW,Shi, JC,Zhang, H,Yang, PY,Wang, XP,&Jin, ZL.(2006).Unsymmetric-1,3-disubstituted imidazolium salt for palladium-catalyzed Suzuki-Miyaura cross-coupling reactions of aryl bromides.journal of molecular catalysis a-chemical,250(1-2),15-19.
MLA Yu, HW,et al."Unsymmetric-1,3-disubstituted imidazolium salt for palladium-catalyzed Suzuki-Miyaura cross-coupling reactions of aryl bromides".journal of molecular catalysis a-chemical 250.1-2(2006):15-19.
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