Total Synthesis of Sordaricin
Year: 2003
Type: article
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.
Source: Organic Letters
DOI: 10.1021/ol0342599
Authors: Lewis N. Mander, Regan J. Thomson
Institution: Australian National University
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
OpenAlex ID: W2171830730
