13C NMR spectra of some symmetrically 2,2′-disubstituted stilbenes: conjugational and conformational effects-Reference-Cited by-同舟云学术

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13C NMR spectra of some symmetrically 2,2′-disubstituted stilbenes: conjugational and conformational effects

Published:1992-03 Issue: Volume:267 Page:405-410
ISSN:0022-2860
Container-title:Journal of Molecular Structure
language:en
Short-container-title:Journal of Molecular Structure

Author:

Vikić-Topić Dražen,Mintas Mladen,Raos Nenad

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference13 articles.

1. The Preparation of Some Unsymmetrically 2,2′ -Disubstituted Stilbenes

2. Effect ofortho substituents in the electron impact induced fragmentation of 2,2′-disubstituted stilbenes

3. CF long range coupling for estimating molecular conformations

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1. Complete1H and13C NMR spectral assignment ofcis- andtrans- 3-{2-[2-(4-methylphenyl)ethenyl]phenyl]}sydnones;Magnetic Resonance in Chemistry;2004

2. 1 H NMR and UV–Vis spectroscopy of chlorine substituted stilbenes: conformational studies;Journal of Molecular Structure;2000-10

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