1 H and  13 C spectral assignment of symmetrical bis[(4‐aminosubstituted)quinolinium] derivatives | Zendy

Campos Joaquín M. | Zendy; SánchezMartín Rosario M. | Zendy; CruzLópez Olga | Zendy; ConejoGarcía Ana | Zendy; Gallo Miguel A. | Zendy; Espinosa Antonio | Zendy

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1 H and 13 C spectral assignment of symmetrical bis[(4‐aminosubstituted)quinolinium] derivatives

Author(s) -

Campos Joaquín M.,

SánchezMartín Rosario M.,

CruzLópez Olga,

ConejoGarcía Ana,

Gallo Miguel A.,

Espinosa Antonio

Publication year - 2005

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.1659

Subject(s) - chemistry , methylene , bibenzyl , dept , ring (chemistry) , stereochemistry , biphenyl , carbon 13 nmr , medicinal chemistry , organic chemistry

1 H and 13 C NMR spectroscopic data of both the quinolinium ring and the spacers for 32 symmetrical bisquinolinium compounds were assigned by a combination of one‐ and two‐dimensional experiments (DEPT, HMBC, HMQC). The compounds have electron‐releasing groups at position 4 of the quinolinium ring, with several arylalkyl linkers such as the 3,3′‐, 4,4′‐bis(methylene)biphenyl and 4,4′‐bis(methylene)bibenzyl moieties. Copyright © 2005 John Wiley & Sons, Ltd.

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