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Total synthesis of sordaricin
Lewis N Mander1, Regan J Thomson
1Research School of Chemistry, Australian National University, Canberra, ACT 0200, Australia. mander@rsc.anu.edu.au
Organic Letters
|April 12, 2003
Abstract:
[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.