Structure elucidation of the oxidation products of 2-arylidene-1-indanones and 2-arylidene-1-benzosuberones

Gábor Tóth, Judit Halász, Sándor Boros, Albert Lévai, Csaba Nemes, Tamás Patonay

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

The relative configuration and stereochemistry of spiroepoxides prepared by dimethyldioxirane, alkaline hydrogen peroxide and m-chloroperoxybenzoic acid and of dione by-products were elucidated by various 1H and 13C NMR methods.

Original languageEnglish
Pages (from-to)932-936
Number of pages5
JournalMagnetic Resonance in Chemistry
Volume34
Issue number11
DOIs
Publication statusPublished - Nov 1 1996

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Keywords

  • C NMR
  • Conformation
  • H NMR
  • Molecular modelling
  • Spiroepoxides

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)

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