1H y 13C NMR spectral characterization of some antimalarial "in vitro" 3-amino-9-methyl-(1H)-pirazolo-[3.4,b]-4-quinoline

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DC Field	Value	Language
dc.contributor.author	Charris, Jaime	-
dc.contributor.author	Domínguez, Jose	-
dc.contributor.author	Lobo, Gricela	-
dc.date.accessioned	2015-01-29T17:09:17Z	-
dc.date.available	2015-01-29T17:09:17Z	-
dc.date.issued	2000-07-05	-
dc.identifier.issn	1043-1802	-
dc.identifier.uri	http://hdl.handle.net/10872/8221	-
dc.description.abstract	We report the 1 HNMRand13 C NMR chemical shifts andJ(H,H), J(H,F) and J(C,F) coupling constants of nine 3-amino-9-methyl-1H-pyrazolo[3,4-b]-4-quinolone derivatives, all of them active againstPlasmodium falciparum in vitro. They were characterized and assigned on the basis of 1 H, 13 Cand13 C–1 H (short- and long-range) correlated spectra. Copyright2000 John Wiley & Sons, Ltd	es_VE
dc.language.iso	en_US	es_VE
dc.publisher	Magneti Resonance in Chemistry	es_VE
dc.subject	MNR	es_VE
dc.subject	1H MNR	es_VE
dc.subject	13C MNR	es_VE
dc.subject	quinolonas	es_VE
dc.subject	antimalarial	es_VE
dc.title	1H y 13C NMR spectral characterization of some antimalarial "in vitro" 3-amino-9-methyl-(1H)-pirazolo-[3.4,b]-4-quinoline	es_VE
dc.type	Article	es_VE
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