Abstract
4-O-Acetyl-2,3-dideoxy-3-tetrabromophthalimido-D-threo-pentopyranosyl chloride (4) was synthesized from the mixture 1-3 by treatment with hydrogen chloride in acetic acid. The structure is confirmed by reaction of 4 to give 4-O-acetyl-3-tetrabromophthalimido-1,2,3-trideoxy-D-threo-pent-1-eno-pyranose (5) and 4-O-acetyl-2,3-dideoxy-3-tetrabromophthalimido-1-[9-(6-phenylamino -2-methylpurinyl)]-ß-D-threo-pentopyranose (6).
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