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
、环碳酸酯、
、脱碳酸酯、酰、环
基甲酸酯和环合
合成目标合物。
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、乙酰、环碳酸酯、、脱碳酸酯、酰、环基甲酸酯和环合合成目标合物。
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