Abstract
(Matrix presented) 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.
Original language | English (US) |
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Pages (from-to) | 1321-1324 |
Number of pages | 4 |
Journal | Organic Letters |
Volume | 5 |
Issue number | 8 |
DOIs | |
State | Published - Apr 17 2003 |
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry