Stereoselective total synthesis of the presumed biosynthetic precursor to lipoxins A and B: methyl (7E,9E,11Z,13E,5S,6S,15S)-5,6-epoxy-15-hydroxyicosa-7,9,11,13-tetra-enoate and its 5,6-methano analogue
- 1 January 1986
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 24,p. 1816-1817
- https://doi.org/10.1039/c39860001816
Abstract
Stereoselective and highly efficient total syntheses of the presumed biosynthetic precursor of lipoxins A and B and its 5,6-methano analogue are described.Keywords
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