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10
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85036682820
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Previous paper in this issue
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Previous paper in this issue
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11
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85036677490
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note
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6 ) are given. ( Bruker AC 200 spectrometer, δ in ppm, TMS as internal standard ). 1b: 8.82 (s, 1H); 7.87 (t, J=5.7Hz, 1H); 5.4 (b.s., 2H); 3.32 (m, 2H); 2.20 (m, 2H). 1c: 8.7 (b.s., 2H); 8.19 (t, J=5.7Hz, 1H); 5.0 (b.s., 2H); 3.44 (m, 2H); 2.57 (t, J=6.5Hz, 2H). 1d: 8.0 (b.s., 1H); 8.1 (b.s., 1H); 8.84 (m, 1H); 3.48 (q, J=6.7Hz, 2H); 2.61 (m, 2H). 1e: 9.55 (b.s., 1H); 9.1 (b.s., 1H); 8.6 (b.s., 1H), 8.26 (t, J=5.8Hz, 1H), 3.50 (m, 2H); 2.79 (s, 3H), 2.57 (m, 2H). 1g: 10.0 (b.s., 2H); 8.29(t, J=5.7Hz, 1H); 3.6-3.9 (m 4H); 3.48 (m, 2H); 2.68 (t, J=6.7Hz, 2H). 1h: 11.80 (b.s., 1H); 8.12 (t, J=5.8Hz, 1H); 6.87 (s, 2H); 3.42 (m, 2H); 2.81 (m, 2H). 1i: 8.12 (b.s., 1H); 7.65 (b.s., 1H); 7.2 (b.s., 4H); 3.1-3.4 (m, 4H). 1j: 8.12 (t, J=5.8Hz, 1H), 4.09 (t, 2H); 2.90 (t, 2H); 2.65 (s, 6H); 1.98 (m, 2H). 1k: 7.96 (t, J=5.9Hz, 1H); 7.34 (b.s., 2H); 3.33 (m, 2H); 2.30 (t, J=7.2Hz, 2H). 1l: 8.34 (t, J=6.0Hz, 1H); 3.40 (m, 2H); 2.72 (t, J=6.4Hz, 2H).1m: 8.08 (t, J=5.8Hz, 1H); 3.30 (m, 8H).
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12
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0000191854
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S. Patai Ed., John Wiley & Sons, N.Y.
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See e.g. :a) Gautier J. A.; Miocque, M.; Combet Farnoux, C. in The chemistry of amidine and imidates S. Patai Ed., John Wiley & Sons, N.Y. 1975, pp 283-348 ;
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Gautier, J.A.1
Miocque, M.2
Combet Farnoux, C.3
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0027473873
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Broggini, M.6
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D'Incalci, M.8
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19
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85036674794
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submitted for publication to
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Marchini, S.; Cozzi, P.; Beria, I.; Geroni, C.; Capolongo, L.; D'Incalci, M.; Broggini, M.; submitted for publication to AnticancerDrug Design.
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AnticancerDrug Design
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Marchini, S.1
Cozzi, P.2
Beria, I.3
Geroni, C.4
Capolongo, L.5
D'Incalci, M.6
Broggini, M.7
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