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
合成目标
合物。