Synthesis of the first example of a nucleoside analogue bearing a 5'-deoxy-D-D-allo-septanose as a seven-membered ring sugar moiety

摘要

The first example of a nucleoside analogue bearing a 5'-deoxy-β-D-allo-septanose as a seven-membered ring sugar moiety, namely 9-(5-deoxy-β-o-allo-septanosyl)-adenine, is reported. This compound was synthesized in 14 steps from the commercially available D-glycero-o-gu/o-1,4-lactone. When evaluated in cell culture experiments against a broad range of viruses, it did not exhibit any significant antiviral effect or cytotoxicity.