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Symmetric 4,6-dialkyl/arylamino-5- nitropyrimidines: theoretical explanation of why aminolysis of alkoxy groups is favoured over chlorine aminolysis in nitro-activated pyrimidines†

dc.contributor.authorPineda De Las Infant Y Villatoro, María José 
dc.date.accessioned2024-01-24T10:11:03Z
dc.date.available2024-01-24T10:11:03Z
dc.date.issued2023-10
dc.identifier.urihttps://hdl.handle.net/10481/87181
dc.language.isoenges_ES
dc.publisherRoyal Society of chemistryes_ES
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs 3.0 Licensees_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es_ES
dc.subjectNitropyrimidineses_ES
dc.subjectPurine Librarieses_ES
dc.titleSymmetric 4,6-dialkyl/arylamino-5- nitropyrimidines: theoretical explanation of why aminolysis of alkoxy groups is favoured over chlorine aminolysis in nitro-activated pyrimidines†es_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1039/d3nj03495j
dc.type.hasVersionVoRes_ES


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