Stereochemical characterization of some mono- and diaryl substituted ethylene oxides by NMR spectroscopy

NMR spectra of several styrene, stilbene and stilbazole oxides have been determined, and chemical shifts and coupling constants have been correlated with cis‐and trans‐configurations. Assignments have been made for all protons, and double resonance technique and 13CH coupling constants have been us...

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Veröffentlicht in:Organic Magnetic Resonance 1970-08, Vol.2 (4), p.379-388
Hauptverfasser: Ceccarelli, Giulio, Berti, Giancarlo, Lippi, Giorgio, Macchia, Bruno
Format: Artikel
Sprache:eng
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Zusammenfassung:NMR spectra of several styrene, stilbene and stilbazole oxides have been determined, and chemical shifts and coupling constants have been correlated with cis‐and trans‐configurations. Assignments have been made for all protons, and double resonance technique and 13CH coupling constants have been used in some particular cases. An explanation is proposed for the observation that chemical shifts of oxirane protons are higher for cis than for trans isomers.
ISSN:0030-4921
1097-458X
DOI:10.1002/mrc.1270020409