A series of 14 3-substituted 4-oxoquinolones with or without a substituent (methyl, ethyl) in position 1 were prepared. Literature and measured data were used to study the inÑuence of the substituent on the shifts of carbon atoms of these compounds, which are model compounds for antibacterial drugs
1H and 13C NMR study of some (E)-3′-and 4′substituted stilben-4-ols
✍ Scribed by Thomas H. Fisher; Tor P. Schultz
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 269 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
A series of ten (E)‐stilben‐4‐ols, HOPhCHCHPhX, with X = H, 4′‐Cl, 4′‐F, 4′‐Me, 4′;‐OMe, 3′‐Me, 3′‐OMe, 3′‐OH, 3′‐F and 3′,4‐diOMe, were studied using one‐ and two‐dimensional NMR techniques. Interpretation of these spectra led to definitive assignments of all carbon and hydrogen chemical shifts. ^1^H chemical shift increments were quantitatively determined for the five substituents studied, and the para A~i~ value of the styryl group was found to be more deshielding than those recorded in previous reports.
📜 SIMILAR VOLUMES
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 ^1^H and ^13^C NMR spectra of 22 2‐substituted 4,5‐dimethylfurans are reported. The __J__(C, H) values were used for signal assignments and for the identification of geometrical isomers of some derivatives.
## Abstract The assignment of all ring carbons of 37 derivatives of 1,3,4‐oxa‐ or thiadiazoles and of seven isosydnones is described. In some cases, ^13^C‐labelled compounds were used. The analysis of substituent effects and the calculation of charge densities of some of the derivatives suggest tha
Jordan 1,3,5-Tris(5-substituted-1,3,4-oxadiazol-2-yl)benzenes were prepared by the dehydration of the corresponding hydrazides. The structures of these compounds were elucidated by IR, 1H and 13C NMR spectroscopy.
## Abstract Dehydration of __N__,__N__′‐diacylalkanedioic acid dihydrazides with phosphoryl chloride gave 5,5′‐disubstituted‐2,2′‐(1,__n__‐alkanediyl)bis‐1,3,4‐oxadiazoles. The structures of these compounds were elucidated by ^1^H, ^13^C NMR, UV and IR spectroscopy.