Synthesis of 6,9α-oxido-11α, 15α-dihydroxyprosta-()5, ()13-dienoic acid, an isomer of PGI2 (vane's PGX)
- 1 January 1977
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 18 (40) , 3529-3532
- https://doi.org/10.1016/s0040-4039(01)83284-6
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Synthesis and stereochemistry of prostacyclin and synthesis of 6-ketoprostaglandin F1.alpha.Journal of the American Chemical Society, 1977
- Nomenclature announcementProstaglandins, 1977
- Synthesis of Vane's prostaglandin X, 6,9.alpha.-oxido-9.alpha.,15.alpha.-dihydroxyprosta-(Z)5,(E)13-dienoic acidJournal of the American Chemical Society, 1977
- The chemical structure of prostaglandin X (prostacyclin)Prostaglandins, 1976
- Arterial walls generate from prostaglandin endoperoxides a substance (prostaglandin X) which relaxes strips of mesenteric and coeliac arteries and inhibits platelet aggregationProstaglandins, 1976
- A lipid peroxide inhibits the enzyme in blood vessel microsomes that generates from prostaglandin endoperoxides the substance (prostaglandin X) which prevents platelet aggregationProstaglandins, 1976
- Arterial walls are protected against deposition of platelet thrombi by a substance (prostaglandin X) which they make from prostaglandin endoperoxidesProstaglandins, 1976
- An enzyme isolated from arteries transforms prostaglandin endoperoxides to an unstable substance that inhibits platelet aggregationNature, 1976
- Superoxide ion as a synthetically useful oxygen nucleophileTetrahedron Letters, 1975
- Protection of hydroxyl groups as tert-butyldimethylsilyl derivativesJournal of the American Chemical Society, 1972