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33847673625
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NMR spectroscopy:
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33847627067
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X-ray crystallography:
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33847607036
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note
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3.
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24
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33847659629
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note
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+, ion-exchange resin) did not improve matters since the α-ribofuranoside was always obtained as the main product.
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25
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33847643260
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0000845917
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1H NMR coupling constants of ring protons of 4 are highly indicative of an all-equatorial substitution pattern. Furthermore, spectral data are nearly identical to those reported for the methyl glycoside:
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1H NMR coupling constants of ring protons of 4 are highly indicative of an all-equatorial substitution pattern. Furthermore, spectral data are nearly identical to those reported for the methyl glycoside:. Sofia M.J., Hunter R., Chan T.Y., Vaughan W., Dulina R., Wang H., and Gange D. J. Org. Chem. 63 (1998) 2802-2803
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30
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33847621198
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note
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It was found that silylation of C-4 could not be fully suppressed in larger scale reactions.
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31
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33847690696
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note
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This compound is very unstable and was used in the next step without purification.
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33
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0033591922
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20444433905
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Asensio J.L., Hidalgo A., Bastida A., Torrado M., Corzana F., Luis Chiara J.L., García-Junceda E., Canãda J., and Jiménez-Barbero J. J. Am. Chem. Soc. 127 (2005) 8278-8279
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40
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33847660065
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note
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Unpublished results.
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42
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33847651784
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note
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1H NMR.
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44
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33847609626
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note
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1,3-Bis-(2,4,6-trimethylphenyl)-(2-imidazolidene)dichloro(O-isopropoxyphenylmethylene)ruthenium.
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