Optically active structural isomers (1b - f and dst-1b - f) of 3′,4′-di-(O)-(-)-camphanoyl-(+)-khellactone (DCK) were synthesized and their anti-human immunodeficiency virus (HIV) activity was investigated. The value of the sensitivity index (SI) of 1b was greater than that of DCK.
- Anti-human immunodeficiency virus
- Asymmetric dihydroxylation
- New Mosher's method
ASJC Scopus subject areas
- Drug Discovery