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., 5:3 (1995), 96

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Mendeleev Communications, 1995, Volume 5, Issue 3, Pages 96–97
DOI: https://doi.org/10.1070/MC1995v005n03ABEH000473 (Mi mendc5047)

This article is cited in 4 scientific papers (total 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

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DOI: https://doi.org/10.1070/MC1995v005n03ABEH000473

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.

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Document Type: Article

Language: English

Citation: 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., 5:3 (1995), 96–97

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https://www.mathnet.ru/eng/mendc/v5/i3/p96

This publication is cited in the following 4 articles:

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