Synthesis of a conformationally locked AZT analogue, 3′-azido-3′-deoxy-2′-O,4′-C-methylene-5-methyluridine
作者:Satoshi Obika、Jun-ichi Andoh、Tomomi Sugimoto、Kazuyuki Miyashita、Takeshi Imanishi
DOI:10.1016/s0040-4039(99)01324-6
日期:1999.8
A bicyclic 3′-azido-3′-deoxythymidine (AZT) analogue with a locked N-conformation, 3′-azido-3′-deoxy-2′-O,4′-C-methylene-5-methyluridine (1a), and its 3′-amino derivative, 3′-amino-3′-deoxy-2′-O,4′-C-methylene-5-methyluridine (1b), were successfully synthesized from D-glucose. The conformation of 1a was also discussed by means of 1H NMR measurements and a molecular modeling (PM3) study.
具有锁定N构象的双环3'-叠氮基3'-脱氧胸苷(AZT)类似物3'-叠氮基3'-脱氧-2'- O,4' - C-亚甲基-5-甲基尿苷(1a)由D-葡萄糖成功合成了其3'-氨基衍生物3'-氨基-3'-脱氧-2'- O,4' - C-亚甲基-5-甲基尿苷(1b)。还通过1 H NMR测量和分子模型(PM3)研究讨论了1a的构象。