Complete  1 H and  13 C NMR spectral assignment of  cis ‐ and  trans ‐ 3‐{2‐[2‐(4‐methylphenyl)ethenyl]phenyl]}sydnones | Zendy

Butković Kristina | Zendy; Marinić Željko | Zendy; ŠindlerKulyk Marija | Zendy

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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

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.

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