Highly enantioselective and diastereoselective synthesis of β-amino acid esters and β-lactams from achiral esters and imines
- 1 September 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (39) , 5287-5290
- https://doi.org/10.1016/s0040-4039(00)92366-9
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- New chiral recognition of chiral tin(II) enolates toward cyclic acyl iminium species. Asymmetric total synthesis of (−)-supinidineTetrahedron Letters, 1988
- A stereocontrolled synthesis of the key intermediate of (+)-thienamycin from ()-(−)-3-hydroxybutyric acid estersTetrahedron Letters, 1987
- A new synthesis of β-lactams from lithium ester enolates andenolizable aldiminesTetrahedron Letters, 1987
- Stereocontrolled total synthesis of the chiral building block (3S,4R)-3- [(R)-1-hydroxyethyl]-4-acetyloxy-azetidin-2-one: a useful synthon for the synthesis of (+)-thienamycin, carbapenems and penems.Tetrahedron Letters, 1985
- Stereocontrolled synthesis of (+)-thienamycin from 3(R)-hydroxybutyric acidTetrahedron Letters, 1985
- Stereoselective synthesis of 3-(1-Hydroxyethyl)-2-azetidinonesfrom 3-hydroxybutyratesTetrahedron Letters, 1984
- N-Trimethylsilylimines: applications to the syntheses of .beta.-lactamsJournal of the American Chemical Society, 1984
- CC bond formation from schiff base and vinyloxyborane: Synthesis of β-amino acid derivativesTetrahedron Letters, 1981
- Preparation of .beta.-lactams by the condensation of lithium ester enolates with aryl aldiminesThe Journal of Organic Chemistry, 1980
- The Reformatsky Reaction with BenzalanilineJournal of the American Chemical Society, 1943