Natural abundance 13C and 15N NMR studies were carried out on a series of N -methylated and N -tert -butylated tetrazoles. Longrange 13C,1H and 15N,1H NMR coupling constants together with 1J (15N,13C) allowed unequivocal assignments of 13C and 15N chemical shifts for isomeric 1,5-and 2,5-disubstitut
15N NMR spectra of wyosine (Y-nucleoside) triacetate and its 7-methyl congener. Chemical shifts and 15N,1H coupling constants
✍ Scribed by C. Glemarec; G. Remaud; J. Chattopadhyaya
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 380 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The 15N chemical shifts and 15N,'H coupling constants of wyosine (Y-nucleoside) triacetate were obtained through both fully proton-coupled and selectively decoupled 15N N M R spectra at natural isotopic abun-dance, using modified INEPT pulse sequences. The spectra were analysed for 2J, and 4J(NH) values. The results were compared with those for the parent compounds.
K E Y W O R D S 1 5 N NMR Wyosine INEPT N,H coupling constants 15N chemical shifts
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