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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.author | Pineda De Las Infant Y Villatoro, María José | |
dc.date.accessioned | 2024-01-24T10:11:03Z | |
dc.date.available | 2024-01-24T10:11:03Z | |
dc.date.issued | 2023-10 | |
dc.identifier.uri | https://hdl.handle.net/10481/87181 | |
dc.language.iso | eng | es_ES |
dc.publisher | Royal Society of chemistry | es_ES |
dc.rights | Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/ | es_ES |
dc.subject | Nitropyrimidines | es_ES |
dc.subject | Purine Libraries | es_ES |
dc.title | Symmetric 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.type | info:eu-repo/semantics/article | es_ES |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | es_ES |
dc.identifier.doi | 10.1039/d3nj03495j | |
dc.type.hasVersion | info:eu-repo/semantics/publishedVersion | es_ES |