Method The target compound was synthesized from clarithromycin via hydrolyzation,acetylation,cyclic carbonatation,oxidation,decarbonatation,acylation,cyclic carbamatation and cyclization.
方法以素为起始原料,经水解、乙酰
、环碳酸酯
、氧
、脱碳酸酯
、酰
、环氨基甲酸酯
和环合等反应合成目标
合物。