New procedures for the synthesis of heterocyclic substituted and 2,4-difunctionalized pyrimidines

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dc.contributor.authorGarcía Martínez, Antonio
dc.contributor.authorHerrera Fernández, Antonio
dc.contributor.authorMoreno Jiménez, Florencio
dc.contributor.authorMuñoz Martínez, Pablo J.
dc.contributor.authorAlonso Martín, Cristina
dc.contributor.authorSubramanian, Laksminarayanapuran R.
dc.date.accessioned2023-06-20T17:22:47Z
dc.date.available2023-06-20T17:22:47Z
dc.date.issued1996-06-03
dc.descriptionReceived in UK 15 March 1996; revised 2 April 1996; accepted 12 April 1996
dc.description.abstractN-Tosyl-2- and -3-acetylpyrrols 1 or N-tosyl-2-pyrrolidone 5 were condensed with cyano compounds in the presence of triflic anhydride (Tf2O) to yield heteroarylpyrimidines. 2,4 Difunctionalized pyrimidines were obtained by reaction of the corresponding 2,4-bis(methylsulfonyl)pyrimidines with nucleophiles.
dc.description.departmentSección Deptal. de Química Orgánica (Óptica y Optometría)
dc.description.facultyFac. de Óptica y Optometría
dc.description.refereedTRUE
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/71217
dc.identifier.doi10.1016/0040-4020(96)00368-7
dc.identifier.issn0040-4020
dc.identifier.officialurlhttps://doi.org/10.1016/0040-4020(96)00368-7
dc.identifier.urihttps://hdl.handle.net/20.500.14352/58170
dc.issue.number23
dc.journal.titleTetrahedron
dc.language.isoeng
dc.page.final7982
dc.page.initial7973
dc.publisherElsevier
dc.rights.accessRightsrestricted access
dc.subject.cdu542.9
dc.subject.cdu66.091
dc.subject.keywordHeterocyclic synthesis
dc.subject.keywordheteroarylpyrimidines.
dc.subject.ucmQuímica orgánica (Química)
dc.subject.unesco2306 Química Orgánica
dc.titleNew procedures for the synthesis of heterocyclic substituted and 2,4-difunctionalized pyrimidines
dc.typejournal article
dc.volume.number52
dspace.entity.typePublication
relation.isAuthorOfPublication0fd1c53c-1da5-428a-8176-a335513eae22
relation.isAuthorOfPublication09111c59-3829-4b92-a9d2-ee099b545e9e
relation.isAuthorOfPublication.latestForDiscovery0fd1c53c-1da5-428a-8176-a335513eae22
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