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Issue 24, 1986
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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

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.

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Article information


J. Chem. Soc., Chem. Commun., 1986, 1816-1817
Article type
Paper

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

K. C. Nicolaou and S. E. Webber, J. Chem. Soc., Chem. Commun., 1986, 1816 DOI: 10.1039/C39860001816

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