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dc.contributor.authorBroumidis, Emmanouilen
dc.contributor.authorKoutentis, Panayiotis Andreasen
dc.creatorBroumidis, Emmanouilen
dc.creatorKoutentis, Panayiotis Andreasen
dc.date.accessioned2019-11-21T06:17:15Z
dc.date.available2019-11-21T06:17:15Z
dc.date.issued2017
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55307
dc.description.abstract3-Deazacanthin-4-one and nine analogues, including the 8-aza analogue, were prepared rapidly and in high yields from 8-iodoquinolones and 2-chloro(het)arylboronic acids. The strategy involves construction of the central B ring via concomitant Pd-catalyzed Suzuki-Miyaura C[sbnd]C and Cu-catalyzed Buchwald-Hartwig C[sbnd]N coupling reactions. © 2017 Elsevier Ltden
dc.sourceTetrahedron lettersen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85020015757&doi=10.1016%2fj.tetlet.2017.05.076&partnerID=40&md5=6de10a363e49cf0d084c3ea749833bf0
dc.subjectBuchwald-Hartwig reactionen
dc.subjectCanthine alkaloidsen
dc.subjectNitrogen heterocyclesen
dc.subjectSuzuki-Miyaura reactionen
dc.subjectTransition-metal catalysisen
dc.titleA one-pot, two-step synthesis of 3-deazacanthin-4-ones via sequential Pd-catalyzed Suzuki-Miyaura and Cu-catalyzed Buchwald-Hartwig reactionsen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.tetlet.2017.05.076
dc.description.volume58
dc.description.issue27
dc.description.startingpage2661
dc.description.endingpage2664
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.abbreviationTetrahedron Lett.en
dc.contributor.orcidKoutentis, Panayiotis Andreas [0000-0002-4652-7567]


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