Enantiospecific synthesis of the fluoro and epimeric derivatives of 5′-noraristeromycin
Abstract
The synthesis of derivatives of 5′-noraristeromycin 1 in which its C-4′ hydroxy group has been (i) replaced by a fluorine atom (5) and (ii) inverted (6) is described starting from the diacetate of (Z)-cyclopentene-3,5-diol.