摘要
Clarithromycin (6-methylerythromycin A, 1) is one of the most important macrolide antibiotics. As the second generation of erythromycin, it is a broad-spectnnn antibiotic with strong antibacterial activity and more favorable phannacokinetic behavior. It has been attracted much attention and shows a bright future in the application and development. The present review describes its synthesis and development, including its discovery, the arts of selective 6-OH-methylation synthesis, various techniques of introduction and elimination of the protective group, diverse routes of clarithromycin preparation and latest synthetic techniques.
源语言 | 英语 |
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页(从-至) | 951-963 |
页数 | 13 |
期刊 | Chinese Journal of Organic Chemistry |
卷 | 22 |
期 | 12 |
出版状态 | 已出版 - 1 12月 2002 |