## Abstract The 270 MHz n.m.r. spectra of phosphoserine (PSer) have been measured and completely analysed for seven pD values. The resulting vicinal coupling constants ^3^__J__(HαHβ) and ^3^__J__(PHβ) are used to discuss the conformations of PSer with respect to the (Hα)CαCβ(O) and (Cα)CβO(P)
Conformational study of phosphoserine in aqueous solution. I—13C n.m.r. results
✍ Scribed by L. Pogliani; D. Ziessow; Ch. Krüger
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 353 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^13^C chemical shifts and coupling constants of phosphoserine in aqueous solutions were studied as a function of pH values. Carboxyl and α‐amino titration shifts agree with those observed in amino acids. The analysis of the coupling constants indicates that for rotation about the (C)CO(P) axis the trans conformer predominates for all pH values. The fractional population of the gauche conformer reaches a maximum at pH=8.
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## Abstract The ^13^C n.m.r. spectra of a variety of purines and 8‐azapurines have been studied in aqueous basic medium; the shifts were measured using dioxane as reference, and corrected to the TMS scale. The compounds studied include adenine, hypoxanthine, 6‐mercaptopurine, guanine, xanthine, 8‐a
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