A highly convergent synthesis of mexiprestil: 16(R) 16-methoxy 16-methyl PGE1 methyl ester
- 31 December 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (51) , 6769-6772
- https://doi.org/10.1016/s0040-4039(00)82450-8
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Triply convergent synthesis of (-)-prostaglandin E2 methyl esterJournal of the American Chemical Society, 1988
- Prostaglandin synthesis. 16. The three-component coupling synthesis of prostaglandinsJournal of the American Chemical Society, 1988
- X-ray structure determination of mexiprostil, A new gastroprotective 16-methoxy-16-methyl-PGE1 analogueProstaglandins, 1988
- Three-Component Coupling Synthesis of Prostaglandins: The Aldol RouteBulletin of the Chemical Society of Japan, 1988
- Radical cyclization-trapping in the synthesis of natural products. A simple, stereocontrolled route to prostaglandin F2.alpha.Journal of the American Chemical Society, 1986
- Structure-activity studies of 16-methoxy-16-methyl prostaglandinsJournal of Medicinal Chemistry, 1986
- Prostaglandin Syntheses by Three‐Component Coupling. New Synthetic Methods (49)Angewandte Chemie International Edition in English, 1984
- Prostaglandin‐Synthesen durch Dreikomponenten‐KupplungAngewandte Chemie, 1984
- Synthesis of prostaglandin D1 and D2 via the three-component coupling processTetrahedron Letters, 1984
- A Facile One-step Synthesis ofcis-2-Cyclopentene- andcis-2-Cyclohexene-1,4-diols from the Corresponding CyclodienesSynthesis, 1974