The M y proton-coupled 15N NMR spectra of pyrimidine with natural isotope abundance and of bis-labelled [1,3-"N2]p~dine, obtained using single pulse experiments, are described. The "N and 'H spectra are analysed for "J, 'J and 4J(NH) as well as N,N and H,H coupling constants.
Low-temperature 15N NMR spectra of reduced 1,3-heterocyclic systems
✍ Scribed by Yoshito Takeuchi; Trevor A. Crabb
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 155 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The "N NMR spectra of the Ginside cis-fused conformer of perhydropyrido[1,2-~][1,3]thiazine shows a shielding of the nitrogen of 23.0 ppm relative to the trans-fused conformer. In contrast, "N shifts for the cisand trans-fused conformers of perhydro-oxazolo[3,4-a]pyridine and perhydrothiazolo[3,4-a]pyridine show corresponding shieldings of only 0.6 and 2.5 ppm, respectively.
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