A short,three-component total synthesis of 12-hydroxyeicosa-5,8,14(Z), 10(E)-tetraenoic acid (12-HETE) via the corresponding ketone
- 1 January 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (45) , 5115-5118
- https://doi.org/10.1016/s0040-4039(01)81538-0
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- The stereochemistry and biosynthesis of hybridalactone, an eicosanoid fromTetrahedron Letters, 1984
- Dicyclohexylphosphide as an auxiliary ligand for thermally stable heterocuprates with considerably improved reactivity. The beneficent effect of lithium bromide on cuprate reactivityThe Journal of Organic Chemistry, 1984
- A new general method for the synthesis of lipoxygenase products: preparation of ±5-HETETetrahedron Letters, 1983
- Chemistry of higher order, mixed organocuprates. 5. On the choice of the copper(I) salt for the formation of R2CuLiThe Journal of Organic Chemistry, 1983
- A new general synthetic route to bridged carboxylic ortho estersTetrahedron Letters, 1983
- Irreversible inhibition of prostaglandin and leukotriene biosynthesis from arachidonic acid by 11,12-dehydro- and 5,6-dehydroarachidonic acids, respectivelyJournal of the American Chemical Society, 1982
- Stereospecific total synthesis of 11(R)-HETE (2), lipoxygenation product of arachidonic acid via the prostaglandin pathwayJournal of the American Chemical Society, 1981
- Chemical and enzymic syntheses of 5-HPETE, a key biological precursor of slow-reacting substance of anaphylaxis (SRS), and 5-HETEJournal of the American Chemical Society, 1980
- Total synthesis of (S)-12-hydroxy-5,8,14-cis,-10-trans-eicosatetraenoic acid (Samuelsson's HETE)Journal of the American Chemical Society, 1978
- Stereospecific synthesis of trisubstituted and tetrasubstituted olefins. Conjugate addition of dialkylcopper-lithium reagents to .alpha.,.beta.-acetylenic estersJournal of the American Chemical Society, 1969