| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5277755 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
The absolute stereochemistry of plakortone E, a cytotoxic metabolite of the Caribbean sponge, was established to be 1, by the synthesis of the racemic C-8 epimer (±)-2 and then of (â)-1 itself, which was identical with the natural compound.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Megumi Akiyama, Yuichi Isoda, Masato Nishimoto, Maiko Narazaki, Hiroaki Oka, Atsuhito Kuboki, Susumu Ohira,