Synthesis of 2′-Substituted Inosine Analogs via Unusual Masking of the 6-Hydroxyl Group
摘要:
2'-Modified inosine analogs have been synthesized from 6-chloropurine riboside via 6-dimethylaminopurine or 6-benzyloxypurine intermediates. The dimethylaminopurine intermediate was obtained via an unusually facile dimethylamine transfer from dimethylformamide.