Please use this identifier to cite or link to this item: http://ri.uaemex.mx/handle20.500.11799/99612
DC FieldValueLanguage
dc.creatorMICHELLE LIZBETH TRUJILLO LAGUNAS-
dc.creatorIGNACIO MEDINA MERCADO-
dc.creatorIVANN ZARAGOZA GALICIA-
dc.creatorHoracio Olivo-
dc.creatorMOISES ROMERO ORTEGA-
dc.date2019-01-15-
dc.date.accessioned2022-04-21T06:01:16Z-
dc.date.available2022-04-21T06:01:16Z-
dc.identifierhttp://hdl.handle.net/20.500.11799/99612-
dc.identifier.urihttp://ri.uaemex.mx/handle20.500.11799/99612-
dc.descriptionEn el presente manuscrito se presenta un método nuevo para la preparación de tetracloropirimidinas y se presenta un estudio acerca de su reactividad química.-
dc.descriptionA convenient two-step synthesis of 2-trichloromethyl-4-chloropyrimidines starting from 2-trichloromethyl-1,3-diazabutadienes is described. These nitrogen heterocycles were prepared in one pot synthesis by a sequential acylation/intramolecular cyclization reaction between 2-trichloromethyl-1,3-diazabutadienes and acyl chlorides in the presence of triethylamine followed by treatment with POCl3. This is the first report for the synthesis of this type of 2-trichloromethyl-4-chloropyrimidine derivatives and serves as a source for a wide variety of other substituted pyrimidines by nucleophilic substitution reactions.-
dc.descriptionConacyt-
dc.languageeng-
dc.publisherThieme-
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/4.0-
dc.source0039-7881-
dc.subjectCycloaddition reaction-
dc.subjecttetrachloropyrimidines-
dc.subject1,3-diazadienes-
dc.subjectintramolecular cyclization-
dc.subjectnucleophilic substitution.-
dc.subjectinfo:eu-repo/classification/cti/2-
dc.titleA Synthesis of 4-Chloro-2-(trichloromethyl)pyrimidines and Their Study in Nucleophilic Substitution-
dc.typearticle-
dc.audiencestudents-
dc.audienceresearchers-
item.grantfulltextnone-
item.fulltextNo Fulltext-
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