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

Research output: Contribution to journalArticle

1 Citation (Scopus)


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
Issue number10
Publication statusPublished - 1987


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

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)

Fingerprint Dive into the research topics of 'Configurational and conformational analysis of norbornane‐and norbornene‐fused 4,1‐oxazepinones'. Together they form a unique fingerprint.

  • Cite this