Method The target compound was synthesized from clarithromycin via hydrolyzation,acetylation,cyclic carbonatation,oxidation,decarbonatation,acylation,cyclic carbamatation and cyclization.
方法以拉霉素为起始原料,经水解、
酰化、环碳酸酯化、氧化、脱碳酸酯化、酰化、环氨基甲酸酯化
环合等反应合成目标化合物。