## Abstract The transmission of electronic effects across the ferrocene analogues of chalcones [3‐aryl‐1‐ferrocenyl‐2‐propene‐1‐ones (series 1) and 1‐aryl‐3‐ferrocenyl‐2‐propene‐1‐ones (series 2)], as well as the conformations of both types of ferrocene analogues have been studied. The ferrocene an
Investigation of substituent effects on the 1H NMR spectra of chalcones
✍ Scribed by E. Solčániová; S. Toma
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 259 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^1^H NMR spectra of 26 substituted chalcones (3‐aryl‐1 phenyl‐2‐propene‐1‐ones and 1‐aryl‐3‐phenyl‐2‐propene‐1‐ones) have been studied. The chemical shifts of the α and β protons to the carbonyl group were correlated with Hammett s̀ parameters. To gain information on the effect of the transmission of the resonance and inductive contributions of the substituents on the chemical shifts of H‐α and H‐β, two parameter correlations with 𝒻 and 𝓇 parameters were also perfomed. The chemical shifts of the aromatic protons of the para‐disubstituted benzene ring correlated with the a~i~ substituent increments.
📜 SIMILAR VOLUMES
## Abstract Correlations with reactivity constants and quantum chemical parameters were used to characterize the substituent effects on the ^1^H NMR spectra of a series of __N__,__N__‐dimethylanilines and __N__,__N__‐diethylanilines. The results indicate that the variations of the chemical shifts o
## Abstract ^13^C chemical shifts for 23 __para__‐ and __meta__‐substituted chalcones of the types **1** and **2** have been determined. The aromatic shieldings are compared with previous results for other aromatic derivatives. Correlations of the ^13^C chemical shifts of vinyl carbons and carbonyl
a See footnote d in Table 1. 'H and "C NMR Spectra of 4 4 - ## Substituted Chalcones KIKUKO HAYAMIZU (to whom correspondence should be addressed), MASARU YANAGISAWA, TETSUKO ISHII,
## Abstract The complete ^1^H and ^13^C NMR spectral assignments of seven positional isomers of __N__,__N__‐dimethylsulfamoylquinolines 2–8 and quinoline have been made using 1D and 2D NMR techniques, including COSY, HMQC and HMBC experiments. Δδ~H~ and Δδ~C~ substituent effects induced by the sulf