## Abstract Phenazopyridine hydrochloride (**1**), a drug in clinical use for many decades, and some derivatives were studied by one‐ and two‐dimensional ^1^H, ^13^C and ^15^N NMR methodology. The assignments, combined with DFT calculations, reveal that the preferred protonation site of the drug is
1H, 13C and 15N NMR assignments for N6-isopentenyladenosine/inosine analogues
✍ Scribed by Silvana Casati; Ada Manzocchi; Roberta Ottria; Pierangela Ciuffreda
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 97 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2641
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✦ Synopsis
Abstract
The complete ^1^H, ^13^C and ^15^N NMR signals assignments of some new isopentenyladenosine analogues were achieved using one‐ and two‐dimensional experiments (gs‐NOESY, gs‐HMQC and gs‐HMBC). Copyright © 2010 John Wiley & Sons, Ltd.
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