Studies directed toward the synthesis of 2'-deoxy-2'-substituted arabino nucleosides

Nucleic Acids Symp Ser. 1987:(18):257-60.

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.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Arabinonucleosides / chemical synthesis*
  • Indicators and Reagents

Substances

  • Arabinonucleosides
  • Indicators and Reagents