A facile synthesis of (−)-prostaglandin E1 via a three-component coupling process
- 31 December 1982
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 23 (39) , 4057-4060
- https://doi.org/10.1016/s0040-4039(00)88695-5
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Observations on the stereochemistry of aldol reaction products. Crystal and molecular structure of erythro-4-(benzoyloxy)-3-tert-butyl-4-phenylbutan-2-oneThe Journal of Organic Chemistry, 1981
- A short, economical, and stereoselective route to prostaglandins by vicinal alkylation of cyclopentadieneJournal of the American Chemical Society, 1981
- Nickel-catalyzed conjugate addition of alkenylzirconium species to .alpha.,.beta.-unsaturated ketonesJournal of the American Chemical Society, 1980
- A convergent total synthesis of (.+-.)-prostaglandin F2.alpha. via conjugate addition and regiospecific enolate trappingThe Journal of Organic Chemistry, 1979
- Asymmetric synthesis via axially dissymetric molecules. 2. A highly efficient synthesis of prostaglandin intermediates possessing the 15S configurationJournal of the American Chemical Society, 1979
- Simple total synthesis of prostaglandins from 4-cumyloxy-2-cyclopentenoneJournal of the American Chemical Society, 1975
- Regiospecific Intramolecular Aldol Condensation Induced by Conjugate Addition of lithium dimethylcuprate to ζ‐Oxo‐α, β‐enones preliminary communication [1]Helvetica Chimica Acta, 1975
- Alkylation of enolate ions generated regiospecifically via organocopper reactions. Synthesis of decalin sesquiterpene valerane and of prostaglandin model systemsJournal of the American Chemical Society, 1975
- Regiospecific Acylation, Alkylation, and Aldol Condensation using magnesium enolates resulting from the conjugate addition of grignard reagents to α, β‐unsaturated ketonesHelvetica Chimica Acta, 1974
- Regiospecific alkylation of organocopper enolatesThe Journal of Organic Chemistry, 1973