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0042665307
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note
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3) δ 1.38 (t, 24H, J = 7.3 Hz), 2.32 - 2.45 (m, 16H), 4.89 - 4.94 (m, 4H), 7.64 (d, 4H, J = 8.1 Hz), 8.12 (t, 4H, J = 7.8 Hz), 9.06 (d, 4H, J = 7.3 Hz).
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14
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0043166275
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note
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With the purification by reprecipitation and column chromatography, the relative yield of the isomer I considerably increased (10 - 15%). For HPLC analyses, the reaction mixtures without the purification were used. The relative yield was calculated from the relative peak height of the isomer I for those of all isomers.
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-
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15
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0041663396
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note
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6) δ 0.90 (t, 24H, J = 7.6 Hz), 1.18 - 1.93 (m, 16H), 4.28 - 4.32(m, 4H), 6.93 (d, 4H, J = 8.1 Hz), 7.53 (t, 4H, J = 7.8 Hz), 8.97 (d, 4H, J = 7.6 Hz).
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-
-
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16
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0043166273
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note
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w = 0.138.
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-
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17
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0001607406
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M. Ashida, N. Uyeda, and E. Suito, Bull. Chem. Soc. Jpn., 39, 2616(1966); C. J. Brown, J. Chem. Soc., 1968, 2488.
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Ashida, M.1
Uyeda, N.2
Suito, E.3
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18
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0041663395
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M. Ashida, N. Uyeda, and E. Suito, Bull. Chem. Soc. Jpn., 39, 2616(1966); C. J. Brown, J. Chem. Soc., 1968, 2488.
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J. Chem. Soc.
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Brown, C.J.1
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19
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37049078999
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I. Chambrier, M. J. Cook, M. Helliwell, and A. K. Powell, J. Chem. Soc., Chem. Commun., 1992, 444; M. J. Cook, J. McMurdo, and A. K. Powell, J. Chem. Soc., Chem. Commun., 1993, 903.
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J. Chem. Soc., Chem. Commun.
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Chambrier, I.1
Cook, M.J.2
Helliwell, M.3
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20
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37049090125
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I. Chambrier, M. J. Cook, M. Helliwell, and A. K. Powell, J. Chem. Soc., Chem. Commun., 1992, 444; M. J. Cook, J. McMurdo, and A. K. Powell, J. Chem. Soc., Chem. Commun., 1993, 903.
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Cook, M.J.1
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