The proton and carbon spectra of the title compounds were completely assigned by the use of 2D NMR techniques including 2D INADEQUATE. Contradictory assignments from the literature were clariÐed and incomplete data completed. The validity of the assignments of proton spectra was checked by computer
Complete assignment of the 1H and 13C NMR spectra of cis and trans isonucleoside derivatives of purine with a tetrahydropyran ring
✍ Scribed by Pedro Besada; Tamara Costas; Carmen Terán
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 78 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2589
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✦ Synopsis
Abstract
^1^H and ^13^C NMR chemical shifts of cis and trans isonucleoside analogues of purine in which the furanose moiety is substituted by a tetrahydropyran ring were completely assigned using one‐ and two‐dimensional NMR experiments that include NOE, DEPT, COSY and HSQC. The significant ^1^H and ^13^C NMR signals differentiating between the cis and trans stereoisomers were compared. Copyright © 2010 John Wiley & Sons, Ltd.
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