Molecules 2012, 17(10), 12121-12139; doi:10.3390/molecules171012121
Article

Suzuki-Miyaura Reactions Catalyzed by C2-Symmetric Pd-Multi-Dentate N-Heterocyclic Carbene Complexes

1,2email, 2email, 2,* email and 1,* email
Received: 20 September 2012; in revised form: 6 October 2012 / Accepted: 9 October 2012 / Published: 16 October 2012
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Suzuki-Miyaura coupling reactions are promoted by Pd complexes ligated with C2-symmetric multi-dentate N-heterocyclic carbenes derived in situ from Pd(OAc)2 and imidazolium salts. Good to excellent yields were obtained for aryl bromides as substrates. Turnover numbers of up to 105 could be achieved with 5 × 10−4 mol% of Pd(OAc)2/1 × 10−3 mol% NHC precatalyst in 24 h.
Keywords: imidazolium salt; N-heterocyclic carbene; palladium; Suzuki-Miyaura coupling; catalysis
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MDPI and ACS Style

Jiang, L.; Shan, F.; Li, Z.; Zhao, D. Suzuki-Miyaura Reactions Catalyzed by C2-Symmetric Pd-Multi-Dentate N-Heterocyclic Carbene Complexes. Molecules 2012, 17, 12121-12139.

AMA Style

Jiang L, Shan F, Li Z, Zhao D. Suzuki-Miyaura Reactions Catalyzed by C2-Symmetric Pd-Multi-Dentate N-Heterocyclic Carbene Complexes. Molecules. 2012; 17(10):12121-12139.

Chicago/Turabian Style

Jiang, Lan; Shan, Fengjun; Li, Zhengning; Zhao, Defeng. 2012. "Suzuki-Miyaura Reactions Catalyzed by C2-Symmetric Pd-Multi-Dentate N-Heterocyclic Carbene Complexes." Molecules 17, no. 10: 12121-12139.


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