## Abstract The ^1^H NMR spectra of 26 nitrated aminopyridines were measured and interpreted. Chemical shift assignments were based on existing chemical shift rules for substituted pyridines and spectral comparison with compounds of similar structure. Some __o__βaminonitropyridines were found to gi
1H NMR spectra of pyranocoumarins
β Scribed by Paolo Manzini; Paolo Rodighiero; Giovanni Pastorini; Adriano Guiotto
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 164 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
The 'H NMR spectra of variously annulated pyranocoumarins are reported. The complete assignment of chemical shifts was achieved by using coupling constants and the shift effects induced by the introduction of methyl groups at various positions on the pyranocoumarin nucleus, and by comparison with the spectra of known compounds.
π SIMILAR VOLUMES
## Abstract The ^1^H NMR Spectra of 28 substituted phenazines have been measured and analysed with computer assistance. Substituent increments of chemical shifts were calculated for methoxy, carbomethoxy and methyl derivatives. The influence of these substituents on coupling constants has been exam
An analysis of the 'H NMR spectra of polyhydroxycarboxylates is presented. Conclusions with regard to the configuration and the conformation are drawn from chemical shifts and vicinal coupling constants.
The 'HNMR spectra of variously annulated methylfurocournarins are reported. The assignment of the chemical shifts for all the protons was achieved by using coupling constants, and shift effects induced by the introduction of methyl groups at various positions on the furocoumarin nucleus.
Carbon-1 3 spectral assignments of five pyrano[3,2-c] [l]benzopyran-5(2H) -ones, five pyrano[2,3-c] [l ]benzopyran-5(2H)ones and five 2-methylfuro[2,3-c] [ l ] benzopyran-4-ones and of 2-methylfuro[3, 2-c] [l]benzopyran-4-one and 4-(2-chloroallyl)-3-hydroxycoumarin were made from mutual correlations