𝔖 Bobbio Scriptorium
✦   LIBER   ✦

1H and 13C NMR study of substituted 3-OH pyridines

✍ Scribed by D.G. De Kowalewski; C. De Los Santos


Book ID
107803281
Publisher
Elsevier Science
Year
1990
Tongue
English
Weight
480 KB
Volume
221
Category
Article
ISSN
0022-2860

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Stereochemical study of hexahydro[1,3]th
✍ Didier Barbry; Guy Ricart; Daniel Couturier πŸ“‚ Article πŸ“… 1981 πŸ› John Wiley and Sons 🌐 English βš– 625 KB

## Abstract Configurations and preferred conformations of a number of hexahydro[1,3]thiazolo[3,2‐__a__]pyridines have been assigned on the basis of their ^1^H and ^13^C NMR spectra. The conformational preferences of these compounds have been interpreted in terms of the minimization of dipolar type

1H, 13C and 17O NMR study of substituted
✍ Erkki Kolehmainen; Katri Laihia; Danuta Rasala; Ryszard Gawinecki πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 English βš– 492 KB πŸ‘ 1 views

## Abstract ^1^H, ^13^C and ^17^O NMR spectra for 22 substituted nitropyridines were measured and their ^1^H NMR spectra were analysed. The most significant variations in the NMR parameters are found for isomeric hydroxy derivatives, owing to the possibility of keto–enol tautomerism. The prevalence

1H, 13C and 15N NMR and IR studies of ha
✍ P. Cmoch; H. Korczak; L. Stefaniak; G. A. Webb πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 85 KB πŸ‘ 1 views

The tetrazole-azide tautomerization of some halogen-substituted tetrazolo [1,5-a]pyridines was examined by IR spectroscopy at ambient temperature and by 1 H, 13 C and 15 N NMR spectroscopy at various temperatures. The tetrazolopyridines can exhibit equilibrium between the azide and the tetrazole for

1H and 13C NMR spectra of 3-substituted
✍ Δ½ubomΓ­r Zalibera; Viktor Milata; DuΕ‘an IlavskΓ½ πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 180 KB πŸ‘ 2 views

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 inΓ‘uence of the substituent on the shifts of carbon atoms of these compounds, which are model compounds for antibacterial drugs