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0031550854
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15
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0037186830
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Merino P., Mates J.A., Revuelta J., Tejero T., Chiacchio U., Romeo G., Iannazzo D., and Romeo R. Tetrahedron Asymmetry 13 (2002) 173
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Chiacchio, U.5
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Iannazzo, D.7
Romeo, R.8
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17
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33747148937
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2.
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20
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33747108506
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The X-Ray CIF files have been deposited at the Cambridge Crystallographic Data Center and allocated with the deposition numbers CCDC 278435 for compound [(S,S,S,S)-11b] and CCDC 278473 for compound [(3R,3aS)-10e].
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21
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0000075203
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Oppolzer W., Kurth M., Reichlin D., Chapuis C., Mohnhaupt M., and Moffatt F. Helv. Chim. Acta 64 (1981) 2802
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Oppolzer, W.1
Kurth, M.2
Reichlin, D.3
Chapuis, C.4
Mohnhaupt, M.5
Moffatt, F.6
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22
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33747120993
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13C-NMR (50 MHz) δ171.2 s, 169.1 s, 150.5 s, 127.6 d, 2C, 125.1 d, 2C, 125.0 d, 81.6 s, 78.3 s, 76.9 d, 75.6 d, 56.9 t, 49.7 t, 42.5 t, 41.1 t, 39.6 d, 34.6 t, 34.1 t, 31.0 t, 27.6 q, 3C, 26.7 q, 26.5 q, 26.4 d 23.7 s, 21.5 q. [(S,S)-8c′] was obtained in mixture with regioisomers (10c)
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23
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0032493775
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Ferreira M.L.G., Pinheiro S., Perrone C.C., Costa P.R.R., and Ferreira V.F. Tetrahedron Asymmetry 9 (1998) 2671
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Ferreira, M.L.G.1
Pinheiro, S.2
Perrone, C.C.3
Costa, P.R.R.4
Ferreira, V.F.5
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24
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33747123722
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Adduct [(R,R)-8d] was recovered in mixture with regioisomers (10d) after chromatography.
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26
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0000617968
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Kim K.S., Kim B.H., Park W.M., Cho S.J., and Mhin B.J. J. Am. Chem. Soc. 115 (1993) 7472
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(1993)
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, pp. 7472
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Kim, K.S.1
Kim, B.H.2
Park, W.M.3
Cho, S.J.4
Mhin, B.J.5
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27
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85004245724
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Imaki K., Niwa H., Sakuyama S., Okada T., Toda M., and Hayashi M. Chem. Pharm. Bull. 29 (1981) 2699
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Imaki, K.1
Niwa, H.2
Sakuyama, S.3
Okada, T.4
Toda, M.5
Hayashi, M.6
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28
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33747103159
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13C NMR (50 MHz) δ174.1 s, 171.2 s, 2C, 171.1 s, 81.6 s, 80.6 s, 68.9 t, 58.1 d, 55.9 q, 55.5 t, 52.7 d, 31.7 t, 29.0 t, 27.8 q, 3C, 24.8 t, 21.6 t.
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32
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33747138011
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13C NMR (100 MHz) δ171.6 s, 170.0 s, 152.6 s, 134.9 s, 129.4 d (2C), 128.9 d (2C), 127.5 d, 82.1 s, 78.7, s, 76.5 d, 67.0 t, 57.3 t, 55.2 d, 43.8 t, 37.8 t, 34.5 t, 27.8 q, 24.0 t.
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