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Condensación de 4-Aminopirimidinas con galactosa

dc.contributor.authorRodríguez, M.
dc.contributor.authorGil, P.
dc.contributor.authorAsenjo, R.
dc.contributor.authorMelgarejo, M.
dc.date.accessioned2023-07-03T10:21:13Z
dc.date.available2023-07-03T10:21:13Z
dc.date.issued1987-03-20
dc.identifier.citationRodríguez, M.; et al. “Condensación de 4-Aminopirimidinas con galactosa”. Ars Pharm, 28(2): 159-163 (1987). Disponible en: https://revistaseug.ugr.es/index.php/ars/article/view/25577es_ES
dc.identifier.issn2340-9894
dc.identifier.urihttps://hdl.handle.net/10481/83075
dc.description.abstractSe obtienen los 4-N-glicósidos II, por reacción de 4-amino-1,6-dihidro-2- metiltio-6-oxo-pirimidina (Ia) y 4-amino-1,6-dihidro-1-metil-2-metiltio-6-oxopirimidina (Ib) con galactosa. Los compuestos II se acetilan con anhidrido acético y piridina, obteniéndose los correspondientes derivados acetilados III.es_ES
dc.description.abstract4-N-glycolsides (11) were prepared by reaction of 4-amino-1 ,6-dihydro-2- methylthio-6-oxo-pyrimidine (la) and 4-amino-1,6-dihydro-1-methylthio-6- oxo-pyrimidine (lb) with galactose. Their acetyl derivatives IIl, were obtained by acetylation of the corresponding II with acetic anhydride and pyridine.es_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.titleCondensación de 4-Aminopirimidinas con galactosaes_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES


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