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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. (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

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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:Faculty of Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry
ID Code:23770
Publisher:Elsevier

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