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、
、环碳酸酯、氧、脱碳酸酯、、环
基甲酸酯和环
等反应成目标
。
碳饱和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、、环碳酸酯、氧、脱碳酸酯、、环基甲酸酯和环等反应成目标。
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