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,经水解、乙酰、环碳酸酯
、
、
碳酸酯
、酰
、环
酸酯
和环合等反应合成目标
合物。