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