Metal directed stereoselective synthesis of 3-(1′-hydroxyethyl)-2-azetidinones from ethyl 3-hydroxybutyrate
- 31 December 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (23) , 3267-3270
- https://doi.org/10.1016/s0040-4039(00)89040-1
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- The ester enolate-imine condensation route to .beta.-lactamsChemical Reviews, 1989
- Formal total synthesis of 1.beta.-methylcarbapenem via a novel route to deoxyamino sugarsThe Journal of Organic Chemistry, 1989
- Literature Review of the Ester Enolate Imine CondensationHETEROCYCLES, 1989
- Complete stereoselective synthesis of chiral intermediates for thienamycin and related antibioticsJournal of the Chemical Society, Chemical Communications, 1988
- A stereocontrolled synthesis of 3-(1′-hydroxyethyl)-2-azetidinones through trimethylsilyl trifluoromethanesulphonate catalyzed condensation of silyl ketene acetal derived from ethyl 3-hydroxybutyrate and imineTetrahedron Letters, 1987
- 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
- On the stereochemical course of vinyloxyborane—imine condensation -the stereoselective formation of threo β-amino acid derivatives-Tetrahedron Letters, 1986
- 3-(1′-hydroxyethyl)-2-azetidinones from 3-hydroxybutyrates and n-arylaldiminesTetrahedron Letters, 1985