Mander Lewis N, Thomson Regan J
Research School of Chemistry, Australian National University, Canberra, ACT 0200, Australia.
Org Lett. 2003 Apr 17;5(8):1321-4. doi: 10.1021/ol0342599.
[structure: see text] The total synthesis of sordaricin, the diterpene aglycone of an important class of antifungal compounds, is described. Two approaches were explored, the first of which utilized a possible biogenetic intramolecular [4 + 2] cycloaddition to form the complete carbon skeleton of the target molecule. A second approach using a tandem cycloreversion/intramolecular [4 + 2] cycloaddition sequence is also detailed.