Method The target compound was synthesized from clarithromycin via hydrolyzation,acetylation,cyclic carbonatation,oxidation,decarbonatation,acylation,cyclic carbamatation and cyclization.
方法以拉霉素为起始原料,经水
、
化、环碳酸酯化、氧化、脱碳酸酯化、
化、环氨基甲酸酯化和环
等反应
成目标化
物。