1 H and  13 C NMR spectral assignments of pyridinium salts linked to a  N ‐9 or  N ‐3 adenine moiety | Zendy

RubioRuiz Belén | Zendy; ConejoGarcía Ana | Zendy; Gallo Miguel A. | Zendy; Espinosa Antonio | Zendy; Entrena Antonio | Zendy

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1 H and 13 C NMR spectral assignments of pyridinium salts linked to a N ‐9 or N ‐3 adenine moiety

Author(s) -

RubioRuiz Belén,

ConejoGarcía Ana,

Gallo Miguel A.,

Espinosa Antonio,

Entrena Antonio

Publication year - 2012

Publication title -

magnetic resonance in chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.483

H-Index - 72

eISSN - 1097-458X

pISSN - 0749-1581

DOI - 10.1002/mrc.3817

Subject(s) - moiety , chemistry , dept , pyridinium , heteronuclear single quantum coherence spectroscopy , nitrogen atom , pyridinium compounds , stereochemistry , carbon 13 nmr , nuclear magnetic resonance spectroscopy , proton nmr , carbon atom , medicinal chemistry , organic chemistry , ring (chemistry)

1 H and 13 C NMR spectral data of 13 new compounds containing a 4‐(dimethylamino)‐ or 4‐(pyrrolidin‐1‐yl)pyridinium moiety linked to the N ‐9 or N ‐3 nitrogen atom of an adenine moiety were assigned. 1D and 2D NMR experiments (DEPT, HSQC and HMBC) allowed the unequivocal identification of N ‐9 and N ‐3 isomers. Copyright © 2012 John Wiley & Sons, Ltd.

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