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Issue 12, 1995

1H and 13C NMR characterization of new oleuropein aglycones

Rita Limiroli,   Roberto Consonni,   Gianluca Ottolina,   Vincenzo Marsilio,   Giorgio Bianchi  and  Lucia Zetta  

Abstract

Enzymatic hydrolysis of oleuropein carried out in a NMR tube, gave two diastereoisomeric aglycones, which have been identified and characterized by proton and carbon NMR experiments in the same aqueous reaction medium. The stereostructures, assigned to the aglycones by NOESY spectroscopy and molecular dynamics calculation are those of two diastereoisomers, 4a and 4b.

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Article information

https://doi.org/10.1039/P19950001519
J. Chem. Soc., Perkin Trans. 1, 1995, 1519-1523
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1 H and 13C NMR characterization of new oleuropein aglycones

R. Limiroli, R. Consonni, G. Ottolina, V. Marsilio, G. Bianchi and L. Zetta, J. Chem. Soc., Perkin Trans. 1, 1995, 1519 DOI: 10.1039/P19950001519

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