A new synthesis of β-phenylaminothioesters and β-lactams base-induced ring-opening of 2-phenyl-3-aryl-5-phenyl-thioisoxazolidines
- 1 January 1993
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 49 (47) , 10965-10976
- https://doi.org/10.1016/s0040-4020(01)80250-7
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- An efficient C2-homologation of aromatic aldehydes via 5-hydroxyisoxazolidinesTetrahedron, 1991
- The ester enolate-imine condensation route to .beta.-lactamsChemical Reviews, 1989
- N,O-heterocyclics13;-14conversion of isoxazolidines into α,β enonesTetrahedron, 1984
- Generation of the enolate of acetaldehyde from non-carbonyl substances and its C-alkylation, O-acylation and O-silylationTetrahedron Letters, 1977
- Carbon acids. 8. The trimethylammonio group as a model for assessing the polar effects of electron-withdrawing groupsThe Journal of Organic Chemistry, 1976
- Carbon acids. 9. The effects of divalent sulfur and divalent oxygen on carbanion stabilitiesThe Journal of Organic Chemistry, 1976
- Evolution de quelques isoxazolidines en milieu basiqueTetrahedron, 1974
- Tetrahydrofuran decomposition. Condensation of solvent fragment with benzophenone and trityllithiumThe Journal of Organic Chemistry, 1973
- Cycloreversions of anions from tetrahydrofurans. Convenient synthesis of lithium enolates of aldehydesThe Journal of Organic Chemistry, 1972
- Condensation of 2-Aryl-1,3-dioxolanes with Alkyllithium Reagents. A New Synthesis of Alkyl Aryl Ketones from Aromatic Aldehydes1The Journal of Organic Chemistry, 1965