Method The target compound was synthesized from clarithromycin via hydrolyzation,acetylation,cyclic carbonatation,oxidation,decarbonatation,acylation,cyclic carbamatation and cyclization.
方法以克拉霉素始
料,经水解、乙酰
、环碳酸
、氧
、脱碳酸
、酰
、环氨基甲酸
环合等反应合成目标
合物。