| Literature DB >> 26828369 |
Karoline Gangestad Primdahl1, Yngve Stenstrøm2, Trond Vidar Hansen3, Anders Vik4.
Abstract
Short and stereoselective syntheses of the two hydroxylated polyunsaturated fatty acid metabolites, namely 5-(S)-HETE and 5-(S)-HEPE, are reported in 23% and 30% overall yields, respectively. In addition, synthesis of the polyunsaturated fatty acid natural product (+)-zooxanthellactone has been achieved in 19% overall yield. The three aforementioned compounds have been conveniently prepared in six steps, starting from the corresponding commercially available polyunsaturated fatty acids arachidonic acid, eicosapentaenoic acid and docosahexaenoic acid, respectively. All three hydroxylated polyunsaturated natural products were prepared using a biomimetic synthesis.Entities:
Keywords: 5-(S)-HDHA; 5-(S)-HEPE; 5-(S)-HETE; Polyunsaturated fatty acids; Stereoselective reduction of enone
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Year: 2016 PMID: 26828369 DOI: 10.1016/j.chemphyslip.2015.12.005
Source DB: PubMed Journal: Chem Phys Lipids ISSN: 0009-3084 Impact factor: 3.329