A highly stereoselective synthesis of a key intermediate of 1β-methylcarbapenems employing the reformatsky reaction of 3-(2-bromopropionyl)-2-oxazolidone derivatives
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (52) , 6625-6628
- https://doi.org/10.1016/s0040-4039(00)96930-2
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Stereoselective synthesis of 1-β-methylcarbapenemTetrahedron Letters, 1987
- A stereoselective approach to 1β-methylcarbapenem antibiotic starting from ()-(−)-3-hydroxybutyric acid esterTetrahedron Letters, 1987
- Stereocontrolled synthesis of an important intermediate for the preparation of 1.beta.-methylcarbapenem antibioticsThe Journal of Organic Chemistry, 1987
- Simple and highly diastereoselective synthesis of a 1β-methylcarbapenem key intermediate involving divalent tin enolatesTetrahedron Letters, 1986
- Simple, stereocontrolled synthesis of 1β-methylcarbapenem antibiotics from 3()-hydroxybutyric acidTetrahedron Letters, 1986
- Lewis acid mediated condensation of chiral imide enolates. A general approach to the synthesis of chiral carbapenem precursorsJournal of the American Chemical Society, 1986
- Highly diastereoselective alkylation onto 4-acetoxy-2-azetidinones employing tin(II) enolates of 3-acyl C-4-chiral 1,3-thiazolidine-2-thionesJournal of the American Chemical Society, 1986
- Synthetic study of 1-substituted carbapenem antibioticsTetrahedron Letters, 1985
- A FACILE, STEREOCONTROLLED ENTRY TO KEY INTERMEDIATES FOR THIENAMYCIN SYNTHESIS FROM ETHYL (S)-3-HYDROXYBUTANOATEChemistry Letters, 1985
- Synthetic Carbapenem Antibiotics. I. 1-b-MethylcarbapenemHETEROCYCLES, 1984