Synthesis of polychlorinated biphenyls and their metabolites with a modified Suzuki-coupling
I Kania-Korwel, S Parkin, LW Robertson, HJ Lehmler
Index: Kania-Korwel, Izabela; Parkin, Sean; Robertson, Larry W.; Lehmler, Hans-Joachim Chemosphere, 2004 , vol. 56, # 8 p. 735 - 744
Full Text: HTML
Citation Number: 23
Abstract
A modified procedure for the synthesis of polychlorinated biphenyls (PCBs) utilizing the Suzuki-coupling, a palladium-catalyzed cross-coupling reaction, is described. The coupling of (chlorinated) benzene boronic acids with bromochlorobenzenes, using Pd (dppf) 2Cl2 (dppf= 1, 1′-bis (diphenylphosphino) ferrocene) as the catalyst and aqueous sodium carbonate as the base, gave the desired PCB congeners in moderate to good yields. ...
Related Articles:
Physical, spectral and chromatographic properties of all 209 individual PCB congeners
[Chemosphere, , vol. 31, # 2 p. 2687 - 2705]
Reactivity features of polychlorobiphenyl congeners in the nucleophilic substitution reactions
[Russian Journal of General Chemistry, , vol. 82, # 1 p. 138 - 143]
Reactivity features of polychlorobiphenyl congeners in the nucleophilic substitution reactions
[Russian Journal of General Chemistry, , vol. 82, # 1 p. 138 - 143]