Stereoselective synthesis of enantiopure 4,5-disubstituted pyrrolidin-2-ones by consecutive cuprate addition and N-acyliminium coupling
- 5 December 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (51) , 7969-7972
- https://doi.org/10.1016/s0040-4039(00)74791-5
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Asymmetric conjugate additions to chiral bicyclic lactams. Synthesis of aracemic trans-2,3-disubstituted pyrrolidinesThe Journal of Organic Chemistry, 1992
- (R)-1-Acetyl-5-isopropoxy-3-pyrrolin-2-one: a versatile chiral dienophile from (S)-malic acidThe Journal of Organic Chemistry, 1992
- Novel stereoselective synthesis of (−)-enterolactone employing chiral unsaturated lactamTetrahedron, 1992
- A potential carbapenem intermediate from L-glutamic acidTetrahedron Letters, 1991
- Regioselective Functionalization of Medium-Ring LactamsSynlett, 1990
- Stereocontrolled Access to all-transα,β,γ-Substituted Pyrrolidinones and Pyrrolidines of High Optical Purity from D-Pyroglutamic AcidSynlett, 1990
- Applications of Higher-Order Mixed Organocuprates to Organic SynthesisSynthesis, 1987
- Organocopper conjugate addition reaction in the presence of trimethylchlorosilaneTetrahedron Letters, 1986
- Conjugate addition of organocopper reagents to n-tosylated α, β-unsaturated amidesTetrahedron Letters, 1985
- Organocopper Conjugate Addition-Enolate Trapping ReactionsSynthesis, 1985