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dc.contributor.authorKalogirou, Andreas S.en
dc.contributor.authorKoutentis, Panayiotis Andreasen
dc.creatorKalogirou, Andreas S.en
dc.creatorKoutentis, Panayiotis Andreasen
dc.date.accessioned2019-11-21T06:19:39Z
dc.date.available2019-11-21T06:19:39Z
dc.date.issued2017
dc.identifier.issn1422-8599
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55615
dc.description.abstract4,6-Dichloro-2-(methylthio) pyrimidine (3) reacts with EtONa in EtOH, at ca. 20 °C, for 2 h, to give exclusively 4-chloro-6-ethoxy-2-(methylthio)pyrimidine (5) in 89% yield. The latter is presented as a useful multifunctionalised pyrimidine scaffold. © 2016 by the authorsen
dc.description.abstractlicensee MDPI, Basel, Switzerland.en
dc.sourceMolBanken
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85009726746&doi=10.3390%2fM923&partnerID=40&md5=240c31907ed52c8b5f4ee37b126bebd1
dc.subjectHeterocycleen
dc.subjectMultifunctionaliseden
dc.subjectPyrimidineen
dc.title4-chloro-6-ethoxy-2-(Methylthio)pyrimidineen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3390/M923
dc.description.volume2017
dc.description.issue1
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Χημείας / Department of Chemistry
dc.type.uhtypeArticleen
dc.source.abbreviationMolBanken
dc.contributor.orcidKoutentis, Panayiotis Andreas [0000-0002-4652-7567]
dc.contributor.orcidKalogirou, Andreas S. [0000-0002-5476-5805]
dc.gnosis.orcid0000-0002-4652-7567
dc.gnosis.orcid0000-0002-5476-5805


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