The synthesis of 2-deoxy-2-fluoro-α-D[6-3H]glucopyranosyl uridine-5′-diphosphate, with the late introduction of the radiolable, has been achieved from 3,4-di-O-benzyl-2-deoxy-2-fluoro-α-D-glucosyl diphenyl phosphate, by an oxidation-reduction sequence, followed by protecting group removal and morpholidate coupling to uridine-5′-monophosphate.
|Number of pages||3|
|Journal||Australian Journal of Chemistry|
|Publication status||Published - 2 Aug 2002|
ASJC Scopus subject areas