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Title: Studies directed toward the synthesis of 2'-deoxy-2'-substituted arabino nucleosides. Author: Pankiewicz KW, Nawrot B, Sochacka E, Watanabe KA. Journal: Nucleic Acids Symp Ser; 1987; (18):257-60. PubMed ID: 3697138. Abstract: Synthesis of the C-nucleoside, 5-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-1-methyluracil, isosteric to the potent antiviral and anticancer nucleoside, 1-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-1-methyluracil (2'-fluoro-5-methyl-ara-U or FMAU) was achieved by exploitation of the 4,5'-anhydro-nucleoside. Attempts at application of this ribosyl-to-arabinosyl pyrimidine transformation to 2,5'-anhydrouridine resulted in the formation of 2,2'-anhydro-5-substituted-arabinosyluracil.[Abstract] [Full Text] [Related] [New Search]