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