Combine the difluorinated carbocyclic analogs with a suitable sugar moiety (e.g., ribose or deoxyribose) to form the nucleoside structure. This may involve glycosidic bond formation.
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(2R,3R)-2,3-dibenzyloxypent-4-enal
BARIUM OXIDE
1,3,4,6-tetra-O-acetyl-2-O-(diphenylphosphoryl)-α-D-glucopyranose
