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,解、乙酰化、环碳酯化、氧化、脱碳酯化、酰化、环氨基甲酯化和环应成目标化物。
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