A novel, general, totally stereoselective one-pot synthesis of cis-3-substituted 4-formylazetidin-2-ones
- 1 February 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (6) , 803-806
- https://doi.org/10.1016/s0040-4039(00)74892-1
Abstract
No abstract availableThis publication has 35 references indexed in Scilit:
- A mild four-carbon homologation of 4-formyl-azetidinonesTetrahedron Letters, 1989
- An asymmetric synthesis of carbapenem antibiotic (+)-PS-5 from ethyl 3-hydroxybutanoateThe Journal of Organic Chemistry, 1988
- The asymmetric synthesis of β-lactam antibiotics-v. Application of chiral α,β-epoxyimines in ketene-imine cycloaddition reactions leading to homochiral 3-aminoazetidinones.Tetrahedron Letters, 1988
- Asymmetric synthesis of (1'R,3R,4R)-4-acetoxy-3-[1'-((tert-butyldimethylsilyl)oxy)ethyl]-2-azetidinone and other 3-(1'-hydroxyethyl)-2-azetidinones from (S)-(+)-ethyl 3-hydroxybutanoate: formal total synthesis of (+)-thienamycinJournal of the American Chemical Society, 1987
- A formal synthesis of aspartame via the oxaziridine - amide rearrangementTetrahedron Letters, 1987
- Enantioselective Syntheses of Carbapenem AntibioticsHETEROCYCLES, 1987
- Stereospecific synthesis of a chiral intermediate for the preparation of thienamycin, penems, and carbapenems: use of the nitro group as a hydroxy protecting groupJournal of the Chemical Society, Perkin Transactions 1, 1986
- An enantioselective approach to carbapenem antibiotics: formal synthesis of (+)-thienamycinTetrahedron Letters, 1985
- OBTENTION D’UN α-AMINO ALDEHYDE OPTIQUEMENT ACTIP EN SERIE β-LACTAMEChemistry Letters, 1984
- Synthesis of Carbapenem AntibioticsHETEROCYCLES, 1982