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,、乙酰化、
碳
酯化、氧化、脱碳
酯化、酰化、
氨基甲
酯化和
反应
成目标化
物。