Triaryl phosphine-functionalized N-heterocyclic carbene ligands for Heck reaction
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Wang, AE
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Nankai Univ, State Key Lab, Inst Elementoorgan Chem, Tianjin, Peoples R ChinaNankai Univ, State Key Lab, Inst Elementoorgan Chem, Tianjin, Peoples R China
Wang, AE
[1
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Xie, JH
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Nankai Univ, State Key Lab, Inst Elementoorgan Chem, Tianjin, Peoples R ChinaNankai Univ, State Key Lab, Inst Elementoorgan Chem, Tianjin, Peoples R China
Xie, JH
[1
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Wang, LX
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Nankai Univ, State Key Lab, Inst Elementoorgan Chem, Tianjin, Peoples R ChinaNankai Univ, State Key Lab, Inst Elementoorgan Chem, Tianjin, Peoples R China
Wang, LX
[1
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Zhou, QL
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Nankai Univ, State Key Lab, Inst Elementoorgan Chem, Tianjin, Peoples R ChinaNankai Univ, State Key Lab, Inst Elementoorgan Chem, Tianjin, Peoples R China
Zhou, QL
[1
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机构:
[1] Nankai Univ, State Key Lab, Inst Elementoorgan Chem, Tianjin, Peoples R China
A new type of triaryl phosphine-functionalized imidazolium salts 6 were prepared. Their palladium complexes, generated in situ, were successfully applied in the palladium-catalyzed Heck reaction. Using 1 mol% of Pd(dba)(2) and 10 mol% 6c in the presence of 2 equiv of K2CO3 in DMAc has proven to be highly efficient for the coupling of a wide array of aryl bromides and iodides with acrylates in excellent yield. The coupling of 4-bromotoluene with various styrene derivatives catalyzed by Pd/6c complex also gave good results. (C) 2004 Elsevier Ltd. All rights reserved.