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.
|Number of pages||6|
|Publication status||Published - 2006 Dec 1|
ASJC Scopus subject areas
- Organic Chemistry