Stereospecific Total Synthesis of Dimorphecolic Acid, 5(S)-HETE, and 12(S)-HETE
- 5 October 1988
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 17 (10), 1785-1788
- https://doi.org/10.1246/cl.1988.1785
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- A highly efficient kinetic resolution of γ- and β- trimethylsilyl secondary allylic alcohols by the sharpless asymmetric epoxidationTetrahedron, 1988
- A highly efficient synthesis of optically pure γ-iodo allylic alcohols and their conversion into various optically active allylic alcoholsTetrahedron Letters, 1987
- Synthesis and physiological activities of both enantiomers of coriolic acid and their geometric isomersTetrahedron Letters, 1987
- A highly efficient synthesis of γ-halo allylic alcohols and propargylic alcohols with high optical purity. Practical method for synthesis of the prostaglandin ω-chainTetrahedron Letters, 1987
- A Convenient Synthesis of (±)-Dimorphecolic Acid and Its AnalogsBulletin of the Chemical Society of Japan, 1986
- A stereoselective synthesis of coriolic acid and dimorphecolic acidTetrahedron, 1986
- Circulating hydroxy fatty acids in familial Mediterranean fever.Proceedings of the National Academy of Sciences, 1985
- Stereospecific synthesis of 5S-HETE, 5R-HETE and their transformation to 5(±)HPETETetrahedron Letters, 1983
- ISOLATION, PROPERTIES, AND STRUCTURAL FEATURES OF DIVALENT CATION IONOPHORES DERIVED FROM BEEF HEART MITOCHONDRIAfn1Annals of the New York Academy of Sciences, 1975
- Nucleophilic ethynyl group equivalent and its use in conjugate addition to .alpha.,.beta.-enonesJournal of the American Chemical Society, 1974