Structure of norbornene‐fused 3,1‐oxazine double cycloadducts

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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.

Original languageEnglish
Pages (from-to)872-876
Number of pages5
JournalMagnetic Resonance in Chemistry
Volume27
Issue number9
DOIs
Publication statusPublished - Sep 1989

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Keywords

  • DNOE, regioselectivity
  • H and C NMR
  • Pentacyclic norbornane/ene‐azetidinone‐fused 3,1‐oxazines, synthesis by cycloaddition

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)

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