Method The target compound was synthesized from clarithromycin via hydrolyzation,acetylation,cyclic carbonatation,oxidation,decarbonatation,acylation,cyclic carbamatation and cyclization.
方法以克拉霉素为起始原料,经水、乙酰
、环碳
、氧
、脱碳
、酰
、环氨基甲
和环
等反应
成目标
物。