ASYMMETRIC NITROGEN - 81 - DIASTEREOMERIC DERIVATIVES OF 1-ALKOXY-2,2-BIS(TRIFLUOROMETHYL)AZIRIDINES - STRUCTURE AND ABSOLUTE-CONFIGURATION

Citation
Av. Prosyanik et al., ASYMMETRIC NITROGEN - 81 - DIASTEREOMERIC DERIVATIVES OF 1-ALKOXY-2,2-BIS(TRIFLUOROMETHYL)AZIRIDINES - STRUCTURE AND ABSOLUTE-CONFIGURATION, Russian chemical bulletin, 47(7), 1998, pp. 1359-1364
Citations number
16
Categorie Soggetti
Chemistry
Journal title
ISSN journal
10665285
Volume
47
Issue
7
Year of publication
1998
Pages
1359 - 1364
Database
ISI
SICI code
1066-5285(1998)47:7<1359:AN-8-D>2.0.ZU;2-Z
Abstract
The H-1 NMR spectra of O-derivatives of 1-hydroxy-2,2-bis (trifluorome thyl)aziridine containing such substituents as EtO2CCH2, (R/S)-RO2CCH( Me) (R = Me, Pr-i, or Bu-t), (R/S)-H2NC(O)CH(Me), and (R)-H2NC(O)CH(Me ) were analyzed. Both of the diastereomerically pure amides of the lat ter type were isolated. The validity of the H-1 NMR criteria, which we re suggested for the determination of absolute configurations of diast ereomers of N-alkoxyaziridines, was confirmed by X-ray diffraction stu dy of the (R,R)-amide.