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The five-membered furan­ose ring of three fluoro- or chloro-substituted 1′-de­oxy-1′-phenyl-β-D-ribo­furan­oses has a conformation between a C2′-endo,C3′-exo twist and a C2′-endo envelope. The ribo­furan­ose groups are connected by O—H...O hydrogen bonds to symmetry-related mol­ecules to form layers. The orientation of the benzene ring is independent of the substitution pattern of the ring and depends mainly on crystal-packing effects.
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