Artículo
The shape of D-glucosamine
Peña, Isabel; Kolesnikova, Lucie; Cabezas, Carlos; Bermudez, Celina; Berdakin, Matias
; Simao, Alcides; Alonso, Jose A.
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Fecha de publicación:
09/2014
Editorial:
Royal Society of Chemistry
Revista:
Physical Chemistry Chemical Physics
ISSN:
1463-9076
Idioma:
Inglés
Tipo de recurso:
Artículo publicado
Clasificación temática:
Resumen
The bioactive amino monosaccharideD-glucosamine has been generated in the gas phasevialaserablation ofD-glucosamine hydrochloride. Three cyclica-4C1pyranose forms have been identified usingFourier transform microwave techniques. Stereoelectronic hyperconjugative forces – essentially linkedwith the anomeric orgaucheeffect – and cooperative OH O, OH N and NH O chains, extendedalong the entire molecule, are found to be the main factors driving the conformational behavior. Theorientation of the NH2group within each conformer has been determined by the values of the nuclearquadrupole coupling constants. The results have been compared with those recently obtained for thearchetypicalD-glucose.
Palabras clave:
Rotational Spectroscopy
,
Laser Desorption
,
Biomolecules
,
D-Glucosamine
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Identificadores
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Articulos(INFIQC)
Articulos de INST.DE INVESTIGACIONES EN FISICO- QUIMICA DE CORDOBA
Articulos de INST.DE INVESTIGACIONES EN FISICO- QUIMICA DE CORDOBA
Citación
Peña, Isabel; Kolesnikova, Lucie; Cabezas, Carlos; Bermudez, Celina; Berdakin, Matias; et al.; The shape of D-glucosamine; Royal Society of Chemistry; Physical Chemistry Chemical Physics; 16; 9-2014; 23244-23250
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