Abstract
(Chemical Equation Presented) Stereoselective synthesis of the C23-C34 fragment of symbiodinolide, which possesses the originally proposed stereochemistry, and its diastereomers was achieved in 19 steps from L-aspartic acid, respectively. Comparison of spectroscopic data of the synthetic products with those of the degraded product of symbiodinolide led to a structural revision of the C23-C34 fragment.
Original language | English |
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Pages (from-to) | 4797-4803 |
Number of pages | 7 |
Journal | Journal of Organic Chemistry |
Volume | 74 |
Issue number | 13 |
DOIs | |
Publication status | Published - Jul 3 2009 |
ASJC Scopus subject areas
- Organic Chemistry