STEREOSELECTIVE RING TRANSFORMATION OF N-ALKYL AZIRIDINES INTO OXAZOLIDIN-2-ONES

Authors
SEPULVEDAARQUES J ARMEROALARTE T ACEROALARCON A ZABALLOSGARCIA E SOLESIO BY CARRERA JE
Citation
J. Sepulvedaarques et al., STEREOSELECTIVE RING TRANSFORMATION OF N-ALKYL AZIRIDINES INTO OXAZOLIDIN-2-ONES, Tetrahedron, 52(6), 1996, pp. 2097-2102
Citations number
12
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron → ACNP
ISSN journal
00404020
Volume
52
Issue
6
Year of publication
1996
Pages
2097 - 2102
Database
ISI
SICI code
0040-4020(1996)52:6<2097:SRTONA>2.0.ZU;2-1
Abstract
N-Alkyl aziridines react stereoselectively with di-tert-butyl dicarbon ate and sodium iodide in acetone to give oxazolidin-2-ones in excellen t yields.