## Abstract The complete ^1^H, ^13^C and ^15^N NMR signals assignment of adenosine derivatives differently substituted at C^6^‐position was achieved using one‐ and two‐dimensional experiments (gs‐COSY, gs‐NOESY, gs‐HSQC and gs‐HMBC). Copyright © 2011 John Wiley & Sons, Ltd.
Restriction of the C6N6 bond rotation of adenosine compounds investigated by1H- and15N-NMR spectra
✍ Scribed by Uzawa, Jun ;Anzai, Kentaro
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 164 KB
- Volume
- 1988
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
If khc C6-N6 bond of an adenosine compound has a partial double bond character as is the case of the 3,5'-cycloadenosine compound 2, the C6-N" bond rotation is restricted, as is observed by 'Hand "N-NMR spectra. ' ) K. Anzai, M. Matsui, Agric. Bid. Chem. Jpn. 37 (1973) 301; *) The signal for acyl-N= is not detected in the "N-INEPT NMR [I 45/88]
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