Prostaglandin Prodrugs III: Synthesis and Biological Properties of C9- and C15CIS-Monoesters of Dinoprost (Prostaglandin F2α)
Author:
Publisher
Elsevier BV
Subject
Pharmaceutical Science
Reference9 articles.
1. Prostaglandin prodrugs I: Stabilization of dinoprostone (prostaglandin E2) in solid state through formation of crystalline C1-phenyl esters
2. Prostaglandin Prodrugs II: New Method for Synthesizing Prostaglandin C1-Aliphatic Esters
3. Total Synthesis of Prostaglandins F2α and E2 as the Naturally Occuring Forms
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1. Studies on a novel series of acyl ester prodrugs of prostaglandin F2 alpha.;British Journal of Ophthalmology;1994-07-01
2. A safe and efficient method for conversion of 1,2- and 1,3-diols to cyclic carbonates utilizing triphosgene;Tetrahedron Letters;1993-01
3. Synthesis and biological activity of prostaglandin lactones;Journal of Medicinal Chemistry;1983-08
4. Prostaglandin Prodrugs VI: Structure-Thermodynamic Activity and Structure-Aqueous Solubility Relationships;Journal of Pharmaceutical Sciences;1980-04
5. ChemInform Abstract: PROSTAGLANDIN PRODRUGS. III: SYNTHESIS AND BIOLOGICAL PROPERTIES OF C9- AND C15-MONOESTERS OF DINOPROST (PROSTAGLANDIN F2α);Chemischer Informationsdienst;1979-12-25
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