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67649379533
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note
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2) were prepared by adopting and modifying the method described in the literature [33]. A solution of 2-pyridinecarboxaldehyde (1 mmol, 0.107 g) in 10 ml of ethanol was added to a solution of 3-aminobenzotrifluoride (1 mmol, 0.160 g) or 3-amino-4-chlorobenzotrifluoride (1 mmol, 0.195 g) dissolved in 10 ml of absolute ethanol while stirring. The resulting mixture was refluxed at 80 °C until the completion of reaction (checked by TLC). The resultant brown coloured liquid was purified by using column chromatography (9:1; ether: chloroform). The solvent was then removed by rotary evaporator to receive brown coloured oily product.
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33
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0034875643
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Iovel I., Golomba L., Belyakov S., Kemme A., and Lukevics E. Appl. Organomet. Chem. 15 (2001) 733
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Lukevics, E.5
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34
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67649362412
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note
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2 (1 mmol, 0.284 g) in 10 ml dichloromethane and stirred for 2 h at room temperature. The volume of solvent was reduced to 4 ml under vacuum. The pale brown coloured complexes were developed by diffusion of diethyl ether into the filtrate.
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35
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4143137875
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Scales S.J., Zhang H., Chapman P.A., McRory C.P., Derrah E.J., Vogels C.M., Saleh M.T., Decken A., and Westcott S.A. Polyhedron. 23 (2004) 2169
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Decken, A.8
Westcott, S.A.9
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37
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33846837475
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Dey, D.K.5
Batten, S.R.6
Jensen, P.7
Yap, G.P.A.8
Mitra, S.9
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0742269665
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Crouse K.A., Chew K.B., Tarafder M.T.H., Kashollah A., Ali A.M., Yamin B.M., and Fun H.K. Polyhedron. 23 (2004) 161
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Yamin, B.M.6
Fun, H.K.7
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41
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67649387016
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note
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General procedure for the amination of aryl halide: 0.05 mmol of copper(I) catalyst was added to 4 mmol of respective aryl amine, 8 mmol of iodobenzene, 12 mmol of KOt-Bu in toluene and the reaction mixture was stirred for 12 h at 90° under nitrogen atmosphere. The reaction mixture was then cooled to room temperature and the solution was filtered to remove the precipitated base. The product was isolated by column chromatography using (9:1) ether: chloroform system to afford desired product.
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26244455979
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Moriwaki, K.1
Satoh, K.2
Takada, M.3
Ishino, Y.4
Ohno, T.5
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