Preparation and NMR determination of structures of tri‐, tetra‐ and pentacyclic isoindolone derivatives

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

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

From the reactions of 3‐endo‐benzoyl‐6‐exo‐phenylbicyclo[2.2.1] heptane‐2‐endo‐carboxylic acid (2) and α,ω‐diamines or o‐aminophenol/thiophenol, different tri‐, tetra‐ and pentacyclic phenyl‐substituted norbornane‐condensed heterocycles were prepared. With ethylenediamine, 2 furnished two isomeric imidazolo[2,1‐a]isoindolones. In the formation of one of them, an end→oexo isomerizaton was observed. The stereostructures (configurations and conformations) of the compounds were elucidated by 1H and 13C NMR spectroscopy, with the aid of routine spectra and also DR, DNOE, DEPT, COLOC and 2D‐HSC measurements.

Original languageEnglish
Pages (from-to)705-710
Number of pages6
JournalMagnetic Resonance in Chemistry
Volume32
Issue number12
DOIs
Publication statusPublished - 1994

Fingerprint

ethylenediamine
Diamines
Nuclear magnetic resonance spectroscopy
Conformations
Nuclear magnetic resonance
Derivatives
Acids
thiophenol
Isoindol-1-one

Keywords

  • C NMR
  • H NMR
  • 2D‐HSC
  • COLOC
  • DEPT
  • DNOE
  • DR
  • NMR
  • Norbornane‐fused O,N‐heterocycles
  • Reaction mechanism
  • Stereostructure

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)

Cite this

Preparation and NMR determination of structures of tri‐, tetra‐ and pentacyclic isoindolone derivatives. / Sohár, P.; Frimpong‐Manso, Samuel; Stájer, G.; Bernáth, G.

In: Magnetic Resonance in Chemistry, Vol. 32, No. 12, 1994, p. 705-710.

Research output: Contribution to journalArticle

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