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Progress in synthesis of clarithromycin

  • Jing Guo Sun*
  • , Jian Hua Liang
  • , Zhi Hua Deng
  • , Guo Wei Yao
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Pages (from-to)951-963
Number of pages13
JournalChinese Journal of Organic Chemistry
Volume22
Issue number12
Publication statusPublished - 1 Dec 2002

Keywords

  • Clarithromycin
  • Review
  • Synthesis

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