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0026642306
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4
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33846341550
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Yoshino, H.; Ueda, N.; Sugumi, H.; Niijima, J.; Kotake, Y.; Okada, T.; Koyanagi, N.; Watanabe, T.; Asada, M.; Yoshimatsu, K.; Iijima, A.; Nagasu, T.; Tsukahara, K.; Kitoh, K. Sulfonamide Derivatives. U.S. Patent 5,250,549, October 5, 1993.
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5
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Eisai Co., previously unpublished results.
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7
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13844280461
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For the synthesis of some glucuronides containing basic functional groups, see:. Kim S., Wu J.Y., Zhang Z., Tang W., Doss G.A., Dean B.J., DiNinno F., and Hammond M.L. Org. Lett. 3 (2005) 411-414
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19
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33947461023
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Compound 5 can be synthesized on multigram scale from 1,2,3,4-tetra-O-acetyl-β-d-glucuronic acid methyl ester in two steps:
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Compound 5 can be synthesized on multigram scale from 1,2,3,4-tetra-O-acetyl-β-d-glucuronic acid methyl ester in two steps:. Bollenback G.N., Long J.W., Benjamin D.G., and Lindquist J.A. J. Am. Chem. Soc. 77 (1955) 3310-3315
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21
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33846377884
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note
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Crystallographic data (excluding structure factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication numbers CCDC627190. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [fax: +44(0) 1223 336033 or e-mail: deposit@ccdc.cam.ac.uk].
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22
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33846386570
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note
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6 (39.5 ppm), 125 MHz): δ 169.5, 169.3, 169.0, 167.1, 162.5, 154.9, 146.7, 131.6, 131.4, 129.3, 126.8, 124.5, 117.3, 116.5, 114.2, 111.4, 96.8, 71.0, 70.9, 70.4, 69.0, 67.0, 55.6, 52.6, 20.3, 20.3, 20.2.
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24
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27444431718
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Lopez Arbeloa F., Banuelos J., Martinez V., Arbeloa T., and Lopez Arbeloa I. Int. Rev. Phys. Chem. 24 (2005) 339-374
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Lopez Arbeloa, F.1
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Arbeloa, T.4
Lopez Arbeloa, I.5
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26
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2342483165
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Klappa J.J., Geers S.A., Schmidtke S.A., Macmanus-Spencer L.A., and McNeill K. Dalton Trans. (2004) 883-891
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Klappa, J.J.1
Geers, S.A.2
Schmidtke, S.A.3
Macmanus-Spencer, L.A.4
McNeill, K.5
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