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、乙酰
、环
酸酯、氧、脱酸酯、酰、环
基甲酸酯和环合等反应合成目标合物。
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、乙酰、环酸酯、氧、脱酸酯、酰、环基甲酸酯和环合等反应合成目标合物。
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