Configurational and conformational analysis of norbornane‐and norbornene‐fused 4,1‐oxazepinones

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Abstract

The preferred conformations and, for the 3‐methyl‐substituted analogues also the configurations of the C‐3 atom, for 3‐unsubstituted and 3‐methyl‐substituted di‐exo‐ and di‐endo‐annellated oxazepinone derivatives fused with a norbornane or norbornene skeleton were determined by 1H and 13C NMR spectroscopy, including the use of DNOE measurements.

Original languageEnglish
Pages (from-to)856-859
Number of pages4
JournalMagnetic Resonance in Chemistry
Volume25
Issue number10
DOIs
Publication statusPublished - 1987

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Keywords

  • H and C NMR DNOE measurements
  • configurations and conformations of norbornane/ene fused oxazepinones
  • Stereostructures

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)

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