Total synthesis of (-)-Pramanicin

Shin ya Aoki, Taro Tsukude, Yukari Miyazaki, Ken ichi Takao, Kin ichi Tadano

Research output: Contribution to journalArticle

11 Citations (Scopus)


The total synthesis of natural (-)-pramanicin, a highly oxygenated γlactam-type antifungal agent, is described. The enantiospecific total synthesis of this natural product commenced with 5-deoxy-1,2-O-isopropylidene-α-d-xylofuranose as an enantiopure starting material.

Original languageEnglish
Pages (from-to)49-54
Number of pages6
Issue number1
Publication statusPublished - 2006 Dec 1

ASJC Scopus subject areas

  • Analytical Chemistry
  • Pharmacology
  • Organic Chemistry

Fingerprint Dive into the research topics of 'Total synthesis of (-)-Pramanicin'. Together they form a unique fingerprint.

  • Cite this

    Aoki, S. Y., Tsukude, T., Miyazaki, Y., Takao, K. I., & Tadano, K. I. (2006). Total synthesis of (-)-Pramanicin. Heterocycles, 69(1), 49-54.