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Progress in synthesis of clarithromycin

  • Jing Guo Sun*
  • , Jian Hua Liang
  • , Zhi Hua Deng
  • , Guo Wei Yao
  • *此作品的通讯作者
  • Beijing Institute of Technology

科研成果: 期刊稿件 › 文章 › 同行评审

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
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

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