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2
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0028443226
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Hashimoto, M.; Isono, T.; Mano, K. Ber. Bunsenges. Phys. Chem. 1994, 98, 793.
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(1994)
Ber. Bunsenges. Phys. Chem
, vol.98
, pp. 793
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Hashimoto, M.1
Isono, T.2
Mano, K.3
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4
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0041937568
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Steinberg, G. M.; Poziomek, E. J.; Hackley, B. E., Jr J. Org. Chem. 1961, 26, 368.
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(1961)
J. Org. Chem
, vol.26
, pp. 368
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Steinberg, G.M.1
Poziomek, E.J.2
Hackley Jr, B.E.3
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6
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37549004176
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Ph.D. Dissertation, University of Innsbruck, Innsbruck, Austria
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Solchinger, A. Ph.D. Dissertation, University of Innsbruck, Innsbruck, Austria, 2006.
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(2006)
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Solchinger, A.1
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7
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37549014697
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A patent claim, although without any experimental proof, has been published: Hayashi, M, Tanouchi, T, Takatsuki; Kawamura, M. I, Kajiwara, I, Iguchi, Y, Takatsuki. German Patent 2917456, 1979
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A patent claim, although without any experimental proof, has been published: Hayashi, M.; Tanouchi, T.; Takatsuki; Kawamura, M. I.; Kajiwara, I.; Iguchi, Y.; Takatsuki. German Patent 2917456, 1979.
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8
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37549014332
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2O, (e) amberlyst/acetone.
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2O, (e) amberlyst/acetone.
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9
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37549004557
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2.
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2.
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10
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37549043331
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Reaction conditions: 4 equiv of DIBAL in hexane solution, 3 h stirring at -70 °C, hydrolysis by dropwise addition of dry methanol at -70 °C.
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Reaction conditions: 4 equiv of DIBAL in hexane solution, 3 h stirring at -70 °C, hydrolysis by dropwise addition of dry methanol at -70 °C.
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11
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37549020494
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Spectroscopic data for 3a: 1H NMR (300 MHz, CD 3SOCD3, δ3.24 (s, 3H, H3C-O, 4.16-4.32 (m, 2H, CH2-N, 4.78 (s, 1H, HO-CHOCH3, 6.67 (br s, 1H, OH, 7.15-7.27 (m, 2H, benzimidazole, 7.59-7.64 (m, 2H, benzimidazole, 8.15 (s, 1H, benzimidazole, 13C NMR (300 MHz, CD3SOCD 3, δ48.97 (CH2-N, 53.81 (H3C-O, 95.07 (HOCH-OCH3, 110.76, 119.23, 121.36, 122.20, 134.31, 143.17, 144.72 (benzimidazole, IR ATR, 3088w, 1499s, 1461m, 1376m, 1260m, 1098m, 1116s, 968m, 883m, 873m, 752s, 636m, 551m cm-1
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-1.
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12
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37549066720
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Spectroscopic data for 3b: 1H NMR (300 MHz, CD 3SOCD3, δ 1.43 (s, 6H, H3C-C, 3.18 (s, 3H, H3C-O, 4.41 (s, 1H, HO-CH-OCH3),6.65 (br s, 1H, OH, 6.82 (s, 1H, imidazole, 7.22 (s, 1H, imidazole),7.66 (s, 1H, imidazole, 13C NMR (300 MHz, CD3SOCD3, δ 23.06 H3C-C, 54.57 (H3C-O, 60.24 (H3C-C, 100.20 (HO-CH-OCH3, 117.91, 127.28, 135.57 (imidazole, IR ATR, 2996w, 1497s, 1389m, 1271s, 1231s, 1124s, 1077s, 1058s, 1027m, 1008s, 921m, 825s, 754s, 664s cm-1
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-1.
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13
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37549072010
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int = 0.0355], final R indices (133 parameters) for 1187 independent reflections [I< 2σ(I)] are R1 = 0.0393, wR2 = 0.0917, GOF = 1.054.
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int = 0.0355], final R indices (133 parameters) for 1187 independent reflections [I< 2σ(I)] are R1 = 0.0393, wR2 = 0.0917, GOF = 1.054.
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14
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0038621565
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Chen, C.-L.; Su, C.-Y.; Cai, Y.-P.; Zhang, H.-X.; Xu, A.-W.; Kang, B.-S.; zur Loye, H.-C. Inorg. Chem. 2003, 42, 3738.
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(2003)
Inorg. Chem
, vol.42
, pp. 3738
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Chen, C.-L.1
Su, C.-Y.2
Cai, Y.-P.3
Zhang, H.-X.4
Xu, A.-W.5
Kang, B.-S.6
zur Loye, H.-C.7
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15
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37549001517
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Crystal data for 4b: C14H22N 4O3 × 2 CH2Cl2 (464.21, orthorhombic, space group Pbcn, a, 1782.14(7, b, 727.22(4, c, 1738.81(9) pm, V, 2.25351(19) nm3, Z, 4, Dc, 1.368 Mg/m 3, μ(Mo-Kα, 0.548 mm-1, T= 233(2) K, 1767 independent reflexes [Rint, 0.0368, final R indices (132 parameters) for 1397 independent reflections [I < 2σI, are R1, 0.0509, wR2, 0.1293, GOF, 1.061
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int = 0.0368], final R indices (132 parameters) for 1397 independent reflections [I < 2σ(I)] are R1 = 0.0509, wR2 = 0.1293, GOF = 1.061.
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