Replacement of the Ribofuranose Oxygen of 2-5A Derivatives by Methylene: Synthesis of an Aristeromycin Analogue of 2-5A Core 5'-Monophosphate (5'-O-Phosphoryladenylyl)(2'->5')adenylyl(2'->5')adenosine

Article abstract of DOI:10.1021/jm00147a048

The ribofuranose oxygens of the the three adenosine residues of the 5'-monophosphate of the 2-5A core 5')adenylyl(2'->5')adenosine> were replaced by methylenes through the synthesis of an aristeromycin <9-<(1R,2S,3R,4R)-2,3-dihydroxy-4-(hydr