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13
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84986676568
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It should be noted that enantiomerically pure compound, 6-epi-COTC ((-)-7), possesses the same absolute stereostructure as the ketocarbasugar, (-)-Gabosine A:
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It should be noted that enantiomerically pure compound, 6-epi-COTC ((-)-7), possesses the same absolute stereostructure as the ketocarbasugar, (-)-Gabosine A:. Bach G., Breiding-Mack S., Grabley S., Hammann P., Huetter K., Thiericke R., Uhr H., Wink J., and Zeeck A. Liebigs Ann. Chem. (1993) 241
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Zeeck, A.9
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19
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34548863515
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note
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Crystallographic data (excluding structure factors) for (±)-11 have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 630924. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [fax: +44 0 1223336033 or e-mail: deposit@ccdc.cam.ac.uk].
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20
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34548853841
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note
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3. Independent reflections (12,286), R1 = 0.0576, wR2 = 0.0821 for 1364 reflections with I > 2σ(I).
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24
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0034620235
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Xia J., Abbas S.A., Locke R.D., Piskorz C.F., Alderfer J.L., and Matta K.L. Tetrahedron Lett. 41 (2000) 169
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Matta, K.L.6
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25
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34548842889
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note
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+) requires 265.0683).
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27
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37049088912
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Hudlicky T., Luna H., Olivo H.F., Andersen C., Nugent T., and Price J.D. J. Chem. Soc., Perkin Trans. 1 (1991) 2907
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Nugent, T.5
Price, J.D.6
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28
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34548862486
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Personal communication: Boyd, D. R.; Sharma, N. D. (unpublished data).
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30
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0023130372
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Carmichael J., DeGraff W.G., Gazdar A.F., Minna J.D., and Mitchell J.B. Cancer Res. 47 (1987) 936
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