Enantioselective synthesis of a new fluoro-substituted HMG-COA reductase inhibitor
- 1 January 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (38) , 5115-5118
- https://doi.org/10.1016/s0040-4039(01)93462-8
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Synthesis of a novel HMG-COA reductase inhibitorTetrahedron Letters, 1988
- A novel short and efficient asymmetric synthesis of statine analoguesTetrahedron Letters, 1988
- Tetrahedron report number 221Tetrahedron, 1987
- Therapeutic Response to Lovastatin (Mevinolin) in Nonfamilial HypercholesterolemiaJAMA, 1986
- 3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 3. 7-(3,5-Disubstituted-[1,1'-biphenyl]-2-yl)-3,5-dihydroxy-6-heptenoic acids and their lactone derivativesJournal of Medicinal Chemistry, 1986
- Convenient two-step stereospecific hydroxy-substitution with retention in β-hydroxy-δ-lactones. 4 ()-heterosubstituted mevinolin and -analogsTetrahedron Letters, 1986
- (R)- and (S)-2-acetoxy-1,1,2-triphenylethanol - effective synthetic equivalents of a chiral acetate enolateTetrahedron Letters, 1984
- STEREOSELECTIVE SYNTHESIS OF MESO(OR ERYTHRO) 1,3-DIOLS FROM β-HYDROXYKETONESChemistry Letters, 1980
- The synthesis of fluorinated carbohydratesPublished by Walter de Gruyter GmbH ,1973
- The Carbon-Fluorine Bond in Compounds of Biological InterestScience, 1969