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0031851335
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Pleier, A-K.; Glas, H.; Grosche, M.; Sirsch, P.; Thiel, W. R. Synthesis, 2001, 55, Dahmani, Z.; Rahmouni, M.; Brugidou, R.; Bazureau, J. P.; Hamelin, J. Tetrahedron Lett., 1998, 39, 8453, Meziane, M. A. A.; Rahmouni, M.; Bazureau, J. P.; Hamelin, J. Synthesis, 1998, 967.
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14
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0005139972
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note
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In this project SmithSynthesizer™ available from Personal Chemistry AB was used. This instrument is fully automated, equipped with temperature and pressure control and can run up to 120 unattended reactions sequentially. The process vial is cooled actively by pressurized air after the irradiation.
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15
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0005134884
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note
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General procedure for the formation on 1a-13a: 2 mmol of 1-13 was mixed with 1.5-2.5 eq. of DMFDEA. DMF was added to a total volume of 5 ml. The reaction mixtures were exposed to microwaves at 180 °C for 5 min and then cooled to room temperature. The residue was split into ten portions for further synthesis without work-up.
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16
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0005185353
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note
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2), 6.82 (dd, 1H, ArH), 6.99 (dt, 1H, ArH), 7. 15 (dt, 1H, ArH), 7.28 (dd, 1H, ArH), 7.47 (m, 5H, ArH), 7.56 (s, 1H, ArH, pyrazole).
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19
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0005143915
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note
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3), 7.53 (m, 3H, phenyl), 7.70 (m, 2H, phenyl), 8.38 (dd, 2H, pyridyl), 8.80 (dd, 2H, pyridyl), 9.16 (s, 1H, pyrimidine).
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20
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0005134384
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note
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2), 7.18 (dd, 1H, ArH), 7.46 (m, 2H, ArH), 7.93 (dd, 1H, ArH), 8.13 (s, 1H, NH), 8.80 (s, 1H, CH).
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