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CCC, which can be substantial, is primarily responsible for this difference.
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C1,C6 values in 3-deoxy-D-ribo-hexopyranoses (αp, 3.0 Hz; βp, 3.4 Hz) exhibit the same truncation as observed in the D-allopyranoses. An axial O3 elicits the same remote effect on the coupling as does an axial hydrogen. The effect thus correlates with the presence of an equatorial electronegative substituent at C3, which enhances the coupling, and not strictly to a change in the C3-O3 bond orientation.
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