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,水解、乙酰化、环碳酸酯化、
化、脱碳酸酯化、酰化、环
基甲酸酯化和环合等反应合成目标化合物。