A convenient and inexpensive conversion of an aziridine to an oxazolidinone
- 14 July 2003
- journal article
- research article
- Published by Elsevier BV in Tetrahedron Letters
- Vol. 44 (29), 5457-5460
- https://doi.org/10.1016/s0040-4039(03)01325-x
Abstract
No abstract availableThis publication has 26 references indexed in Scilit:
- A Novel Synthesis of 5-Functionalized Oxazolidin-2-ones from Enantiomerically Pure 2-Substituted N-[(R)-(+)-α-Methylbenzyl]aziridinesThe Journal of Organic Chemistry, 2002
- Iron Carbonyl Promoted Conversion of an Aziridine and an Amine Oxide to a 1,2-DiamineOrganometallics, 2002
- Novel Stereoselective Synthesis of Functionalized Oxazolidinones from Chiral AziridinesThe Journal of Organic Chemistry, 2002
- Electrosynthesis of cyclic carbamates from aziridines and carbon dioxideChemical Communications, 2000
- N,Se-Acetals: Preparation and use in diastereoselective radical reactionsHelvetica Chimica Acta, 1998
- 1,3-Oxazolidin-2-ones from 1H-aziridines by a novel stratagem which mimics the direct insertion of CO2Journal of the Chemical Society, Perkin Transactions 1, 1991
- Regioselective cycloaddition of 1,2‐disubstituted aziridines to heterocumulenes catalyzed by organoantimony halidesEuropean Journal of Inorganic Chemistry, 1989
- A General Method for Stereo- and Regio- Specific Oxyamination of OlefinsSynthetic Communications, 1988
- Reaction of Carbon Dioxide with 1-Phenylaziridine Catalyzed by Organo-antimony and -tin CompoundsBulletin of the Chemical Society of Japan, 1985
- A new synthetic route to 2-oxazolidonesJournal of the Chemical Society, Chemical Communications, 1976