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1
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85163228082
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S. Darses, G. Michaud, J. Genêt, Eur. J. Org. Chem. 1999, 1875-1883.
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S. Darses, G. Michaud, J. Genêt, Eur. J. Org. Chem. 1999, 1875-1883.
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4
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14544288182
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V. Gallo, P. Mastrorilli, C. F. Nobile, R. Paolillo, N. Taccardi, Eur. J. Inorg. Chem. 2005, 582-588.
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Gallo, V.1
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Nobile, C.F.3
Paolillo, R.4
Taccardi, N.5
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5
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85163231431
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The role of the ionic liquid in generating the active species has already been ruled out in our system see ref.[3
-
[3]).
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6
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26844485585
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and references cited therein
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L. S. Santos, L. Knaack, J. O. Metzger, Int. J. Mass. Spectrom. 2005, 246, 84-104 and references cited therein.
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Santos, L.S.1
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25144508880
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Guo, H.1
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Sabino, A.A.1
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12
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13
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85163224424
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0-catalysed cross-coupling reactions between arenediazonium salts and potassium organotrifluoroborates appeared after submission of this manuscript: J. Masllorens, I. González, A. Roglans, Eur. J. Org. Chem. 2007, 158-166.
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0-catalysed cross-coupling reactions between arenediazonium salts and potassium organotrifluoroborates appeared after submission of this manuscript: J. Masllorens, I. González, A. Roglans, Eur. J. Org. Chem. 2007, 158-166.
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14
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85163223244
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1H NMR spectra of the reaction solution were poorly informative due to the overlap of phenyl signals coming from the ligand and the borate species.
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1H NMR spectra of the reaction solution were poorly informative due to the overlap of phenyl signals coming from the ligand and the borate species.
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15
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85163233607
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19F NMR spectrum of a methanol suspension of 4 was recorded at 50°C.
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19F NMR spectrum of a methanol suspension of 4 was recorded at 50°C.
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18
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85163225042
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See electronic supporting information (Figure S25).
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See electronic supporting information (Figure S25).
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19
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0000047592
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22
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85163234912
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Diazonium salts are known to undergo radical reactions with acetate ions that lead to decomposition products: H. Zollinger, Azo and Diazo Chemistry, Aliphatic and Aromatic Compounds, Interscience Publishers, London, 1961, p. 153
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Diazonium salts are known to undergo radical reactions with acetate ions that lead to decomposition products: H. Zollinger, Azo and Diazo Chemistry, Aliphatic and Aromatic Compounds, Interscience Publishers, London, 1961, p. 153.
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