## Abstract 2,3,8,9,10,11‐Hexahydro‐7__H__‐dibenzo[__de,h__]quinolin‐7‐one, 5‐methoxy‐2,3,8,9,10,11‐hexahydro‐7__H__‐dibenzo[__de,h__]quinolin‐7‐one, 5‐methoxy‐6‐hydroxy‐1,2,3,7a,8,9,10,11,11a,11b‐decahydro‐7__H__‐dibenzo[__de,h__]quinolin‐7‐one, 5‐methoxy‐5,6,8,9,10,11‐hexahydro‐4__H__‐dibenzo[__d
Complete 1H and 13C NMR spectral assignment of α- and β-adenosine, 2′-deoxyadenosine and their acetate derivatives
✍ Scribed by P. Ciuffreda; S. Casati; A. Manzocchi
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 108 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2036
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✦ Synopsis
Abstract
^1^H and ^13^C NMR chemical shifts of α‐ and β‐anomers of adenosine, 2′‐deoxyadenosine and their acetate derivatives were completely and definitely assigned using the concerted application of one‐ and two‐dimensional experiments (gCOSY, gNOESY, gHSQC and gHMBC). The influence of the stereochemistry of the purine base on the NMR data of the hydrogen and carbon atoms of the furanose moiety was estimated. Copyright © 2007 John Wiley & Sons, Ltd.
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