Abstract
Stereoselective synthesis of the AB-ring fragment of gambieric acid A has been accomplished, wherein (i) an acetylide-aldehyde coupling for fragment assembly and (ii) construction of the tetrahydrofuran A-ring via a diastereoselective bromoetherification were successfully employed as key transformations.
Original language | English |
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Pages (from-to) | 139-144 |
Number of pages | 6 |
Journal | Heterocycles |
Volume | 72 |
DOIs | |
Publication status | Published - 2007 Apr 13 |