E. Butkus, U. Berg, A. Stoncius, A. Zilinskas, “Chromatographic Separation and Absolute Configuration of Chiral Methyl 2-Oxobicyclo[3.2.1]octane-6-carboxylate”, Mendeleev Commun., 1995, Volume 5, Issue 3,Pages <nobr>96

This article is cited in 4 papers

Chromatographic Separation and Absolute Configuration of Chiral Methyl 2-Oxobicyclo[3.2.1]octane-6-carboxylate

E. Butkus^a, U. Berg^b, A. Stoncius^a, A. Zilinskas^a

^a Institute of Chemistry, Vilnius University, Vilnius, Lithuania
^b Department of Organic Chemistry, Centre for Chemistry and Chemical Technology, Lund University, Lund, Sweden

Abstract: Enantiomer separation of methyl exo-2-oxobicyclo[3.2.1]octane-6-carboxylate 2 has been achieved by liquid chromatography on swollen microcrystalline triacetylcellulose and the absolute configuration of (−)-2 and ( + )-2 assigned using circular dichroism spectra.

Language: English

DOI: 10.1070/MC1995v005n03ABEH000473