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Structure of a norbornane‐fused pentacyclic isoxazoline

descriptionPublicationkeyboard_double_arrow_right Article 01 Dec 1990 Hungary English Publisher:WileyJournal:Magnetic Resonance in Chemistry, volume 28, pages 1,023-1,026 (issn: 0749-1581, eissn: 1097-458X,

Authors: Sohár Pál; Kövesdi István; Frimpong-Manso Samuel; Stájer Géza; Bernáth Gábor;

doi: 10.1002/mrc.1260281205

Structure of a norbornane‐fused pentacyclic isoxazoline

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Abstract

AbstractThe steric structure of a pentacyclic adduct formed as a by‐product in a retro‐Diels‐Alder reaction was elucidated by 1H and 13C NMR spectroscopy, making use of double resonance and differential nuclear Overhauser effect measurements.

Country

Hungary

Related Organizations

University of Szeged
Hungary
Albert Szent-Györgyi Medical University
Romania
Egis Group
France
Egis Pharmaceuticals (Hungary)
Hungary

Keywords

03.02. Klinikai orvostan

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