Structure of a norbornane‐fused pentacyclic isoxazoline

P. Sohár, István Kövesdi, Samuel Frimpong‐Manso, G. Stájer, G. Bernáth

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

The 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.

Original languageEnglish
Pages (from-to)1023-1026
Number of pages4
JournalMagnetic Resonance in Chemistry
Volume28
Issue number12
DOIs
Publication statusPublished - 1990

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Keywords

  • DNOE DEPT
  • Pentacyclic isoxazoline fused with norbornane‐norbornene skeleton
  • Stereostructure by NMR H and C NMR spectra
  • Synthesis by double cycloaddition

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)

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