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Complete 1 H and 13 C NMR spectral assignment of cis ‐ and trans ‐ 3‐{2‐[2‐(4‐methylphenyl)ethenyl]phenyl]}sydnones
Author(s) -
Butković Kristina,
Marinić Željko,
ŠindlerKulyk Marija
Publication year - 2004
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/mrc.1488
Subject(s) - chemistry , chloroform , benzene , deuterium , nmr spectra database , carbon 13 nmr , acetone , deuterium nmr , nuclear magnetic resonance spectroscopy , proton nmr , spectral line , medicinal chemistry , stereochemistry , organic chemistry , physics , quantum mechanics , astronomy
Abstract 1 H and 13 C NMR spectra of cis ‐ and trans ‐3‐{2‐[2‐(4‐methylphenyl)ethenyl]phenyl]}sydnones, the first stilbene‐substituted mezoionic oxadiazolium rings, were fully assigned combining the information in various solvents, such as deuterated benzene, acetone and chloroform, using 2D NMR techniques. Copyright © 2004 John Wiley & Sons, Ltd.