Journal
ORGANIC LETTERS
Volume 5, Issue 8, Pages 1321-1324Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol0342599
Keywords
-
Categories
Ask authors/readers for more resources
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.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available