Accessibility navigation


Diastereoselective formation of 2-aryl-3-arenesulfonyl 4-ethyl-1,3-oxazolidines: an X-ray crystallographic and 1H NMR study

Kumar, G. B., Patel, H. V., Shah, A. C., Trenkle, M. and Cardin, C. J. ORCID: https://orcid.org/0000-0002-2556-9995 (1996) Diastereoselective formation of 2-aryl-3-arenesulfonyl 4-ethyl-1,3-oxazolidines: an X-ray crystallographic and 1H NMR study. Tetrahedron: Asymmetry, 7 (12). pp. 3391-3396. ISSN 0957-4166

Full text not archived in this repository.

It is advisable to refer to the publisher's version if you intend to cite from this work. See Guidance on citing.

To link to this item DOI: 10.1016/S0957-4166(96)00446-6

Abstract/Summary

N-Arylsulfonamides of (R)- and (S)-2-amino-1-butanol, on condensation with aromatic aldehydes produced diastereomerically pure 2-aryl-3-arenesulfonyl 4-ethyl-1,3-oxazolidines. The absolute configurations of one enantiomeric pair have been determined from two fully refined X-ray structures, supplemented by nmr data.

Item Type:Article
Refereed:Yes
Divisions:Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry
ID Code:23770
Publisher:Elsevier

University Staff: Request a correction | Centaur Editors: Update this record

Page navigation