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dc.contributor.authorMelgarejo Sampedro, Miguel
dc.contributor.authorRico Gómez, R.
dc.date.accessioned2023-06-01T11:55:26Z
dc.date.available2023-06-01T11:55:26Z
dc.date.issued1982-09-20
dc.identifier.citationMelgarejo Sampedro, M.; Rico Gómez, R. Preparación de 5-β-(3-desoxi-3-nitro)-glucopiranosil-4,5-diacetamido uracilos. Ars Pharm, 23(4): 481-487 (1982). [https://revistaseug.ugr.es/index.php/ars/article/view/25060]es_ES
dc.identifier.issn2340-9894
dc.identifier.urihttps://hdl.handle.net/10481/82110
dc.description.abstractLa re:ción de alfa-(R )-(4, 5-diacetamido-1, 3-dimetil-2, 6-dioxo-1, 2, 3, 6-tetrahidropirimidin-5-il), alfa-(R)-hidroximetil diglocolaldehido con nitrometano produce una mezcla de 5-N-,8-D-(3-nitro-3-desoxi-)-glicopiranosil-4, 5-diacetamido uracilos. De esta mezcla se ha podido aislar el derivado gluco. También se preparan diferentes derivados acetilados. La estructura de dichos compuestos ha sido demostrada por espectroscopia de masas, l. R. Y R. M. N. 60 Y 200 MHz.es_ES
dc.description.abstractThe reaction of alpha-(RH 4, 5-diacetamido-1, 3-dimethyl 2,6-dioxo-1, 2, 3, 6- tetrahydropyrimidine-5-yl), alpha-(R)-hydroxymethyl diglycolaldehyde with nitro. methane yielded a mixture of 5-N-,8-D-(3-desoxi-3-nitro-)-glycopyranosyl-4 · , 5- diacetamido uracils. From this mixture, the gluco-derivate was removed. Sorne acetyl-derivates were prepared. The structure of these compounds was demonstrated by Mass, I. R. and N. M. R. 60 and 200 MHz spectroscopiees_ES
dc.language.isospaes_ES
dc.publisherUniversidad de Granada, Facultad de Farmacia.es_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titlePreparación de 5-β-(3-desoxi-3-nitro)-glucopiranosil-4,5-diacetamido uraciloses_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.30827/ars


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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