Stereostructural and NMR study of isomeric oxazines fused to the norbornane or norbornene skeleton

P. Sohár, István Pelczer, G. Stájer, G. Bernáth

Research output: Contribution to journalArticle

28 Citations (Scopus)

Abstract

Norbornane‐ or norbornene‐fused 2‐aryldihydro‐1,3‐oxazines, ‐1,3‐oxazin‐2‐ones and – 1,3‐oxazine‐2‐thiones were synthesized and studied by 1H and 13C NMR spectroscopy to reveal the spectral effects of the saturation of the skeleton, diexo or diendo ring annellation and isomerism in compounds containing the oxygen and nitrogen hetero atoms in isomeric positions.

Original languageEnglish
Pages (from-to)584-591
Number of pages8
JournalMagnetic Resonance in Chemistry
Volume25
Issue number7
DOIs
Publication statusPublished - 1987

Fingerprint

Norbornanes
Oxazines
Nuclear magnetic resonance spectroscopy
Nitrogen
Nuclear magnetic resonance
Oxygen
Atoms
2-norbornene

Keywords

  • H and C NMR
  • 2‐aryl‐dihydro‐1,3‐oxazines fused to norbornane/ene skeleton
  • diexo and diendo annellation
  • structural isomerism

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)

Cite this

Stereostructural and NMR study of isomeric oxazines fused to the norbornane or norbornene skeleton. / Sohár, P.; Pelczer, István; Stájer, G.; Bernáth, G.

In: Magnetic Resonance in Chemistry, Vol. 25, No. 7, 1987, p. 584-591.

Research output: Contribution to journalArticle

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