摘要
New structural phospholipids 1.3-cyclic monoalkyl(acyl)-rac-glycerothiophosphates of uridine were synthesized. The strategy for the synthesis is using hexaethylphosphorous triamide, activated by a catalytic amount of iodine, as the phosphorylating reagent. Their structures were confirmed by (1)HNMR, (31)PNMR, IR and elemental analysis.
New structural phospholipids 1.3-cyclic monoalkyl(acyl)-rac-glycerothiophosphates of uridine were synthesized. The strategy for the synthesis is using hexaethylphosphorous triamide, activated by a catalytic amount of iodine, as the phosphorylating reagent. Their structures were confirmed by (1)HNMR, (31)PNMR, IR and elemental analysis.
