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17 NMR analysis of this mixture was further complicated by the formation of a new chiral center of the aminoacetal.
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18 Daniels, P.J.L., Mallams, A.K., Wright, J.J., J. Chem. Soc. Chem. Commun., 1973, 675-676; Arcamone, F., Bargiotti, A., Cassinelli, G., Redaelli, S., Hanessian, S., Di Marco, A., Casasza, A.M., Dasdia, T., Necco, A., Reggiani, P., Supino, R., J. Med. Chem., 1976, 19, 733-734; Tsai, T.Y.R., Jin, H., Wiesner, K., Can. J. Chem., 1984, 62, 1403-1405; Wiesner, K., Tsai, T.Y.R., Jin, H., Helv. Chim. Acta, 1985, 68, 300-314.
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19 Tanemura, K., Suzuki, T., Horaguchi, T., J. Chem. Soc. Chem. Commun., 1992, 979-980.
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35
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0010403339
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note
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3,2eq 2.5 Hz, H-3B).
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36
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0010366275
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note
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3) 192.05, 150.31, 143.62, 132.92, 130.30, 117.69, 109.98, 99.68, 97.78, 94.32, 81.85, 77.50, 71.19, 68.76, 68.03, 66.05, 64.27, 61.89, 60.97, 60.69, 55.14, 51.96, 49.21, 44.02, 27.74, 26.76, 24.91, 19.23, 18.31, 14.75.
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37
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0010397646
-
-
note
-
3) 192.22, 151.38, 150.63, 142.98, 133.45, 130.44, 129.20, 120.17, 102.56, 99.77, 97.28, 93.46, 80.82, 71.12, 70.38, 69.03, 68.18, 66.97, 61.66, 60.89, 57.18, 54.90, 51.95, 47.54, 25.33, 19.26, 18.38, 17.55.
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23 Krishnamurthy, G., Ding, W.D., O'Brien, L., Ellestad, G.A., Tetrahedron, 1994, 50, 1341-1349.
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