A novel, double-asymmetric aldol approach to the synthesis of a 1β-methyl carbapenem antibiotic precursor
- 31 December 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (49) , 6461-6463
- https://doi.org/10.1016/s0040-4039(00)82373-4
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Stereoselective synthesis of 1-β-methylcarbapenemTetrahedron Letters, 1987
- A stereoselective approach to 1β-methylcarbapenem antibiotic starting from (Tetrahedron Letters, 1987
- A new approach to the chiral synthesis of the 1-.beta.-methylcarbapenem key precursor using an achiral ketone Sn(II) enolateThe Journal of Organic Chemistry, 1987
- Simple and highly diastereoselective synthesis of a 1β-methylcarbapenem key intermediate involving divalent tin enolatesTetrahedron Letters, 1986
- A stereocontrolled route to optically active 1-methyl carbapenemsTetrahedron 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
- A novel and efficient synthesis of the key intermediate of 1β-methylcarbapenem antibiotics from ()-methyl 3-hydroxy-2-methylpropionateTetrahedron Letters, 1986
- Synthetic carbapenem antibiotics III. 1-Methyl thienamycinTetrahedron Letters, 1985
- Synthetic Carbapenem Antibiotics. I. 1-b-MethylcarbapenemHETEROCYCLES, 1984