Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5220753 | Tetrahedron | 2011 | 16 Pages |
Abstract
A stereocontrolled synthesis of a fully elaborated GHIJ-ring fragment of gambieric acids, which are potent antifungal polycyclic ether natural products, has been accomplished. The synthesis features convergent assembly of the tetracyclic polyether skeleton through aldol coupling/cyclodehydration/reductive etherification processes and stereoselective construction of the J-ring side chain by a CeCl3-promoted Julia-Kocienski olefination.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Koichi Tsubone, Keisuke Hashizume, Haruhiko Fuwa, Makoto Sasaki,