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Structure of norbornene-fused 3,1-oxazine double cycloadducts
Authors:Pál Sohár  Gábor Bernáth  Géza Stájer  Angela E. Szabo
Affiliation:1. Spectroscopic Department, EGIS Pharmaceuticals, P.O.B. 100, H-1475 Budapest, Hungary;2. Institute of Pharmaceutical Chemistry, Albert Szent-Györgyi Medical University, P.O.B. 121, H-6701 Szeged, Hungary
Abstract:
Pentacyclic isoxazolines were obtained by the cycloaddition of benzonitrile oxide to norbornene-azetidinone-fused 3,1-oxazines. The constitutions of two of the isomers obtained, and the configurations and conformations of all products, were determined by means of 1H and 13C NMR spectroscopy and DNOE experiments.
Keywords:Pentacyclic norbornane/ene-azetidinone-fused 3,1-oxazines, synthesis by cycloaddition  1H and 13C NMR  DNOE, regioselectivity
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