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dc.contributor.authorBerezin, Andrey A.en
dc.contributor.authorKoutentis, Panayiotis Andreasen
dc.creatorBerezin, Andrey A.en
dc.creatorKoutentis, Panayiotis Andreasen
dc.date.accessioned2019-11-21T06:16:52Z
dc.date.available2019-11-21T06:16:52Z
dc.date.issued2011
dc.identifier.issn1422-8599
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55294
dc.description.abstract8-Bromo-4H-[1,2,4]oxadiazolo[3,4-c][1,4]benzoxazin-1-one 1 (NS2028) reacts with [2-chloro-5-(trifluoromethyl)phenyl]boronic acid 2 (2 equiv), Pd(OAc)2 (10 mol%) and KOAc (4 equiv) in acetonitrile heated to ca. 110 °C (sealed tube) for 12 hours to give 8-[2-chloro-5-(trifluoromethyl)phenyl]-4H-[1,2,4]oxadiazolo[3,4-c][1,4]benzoxazin-1-one 4 in 64% yield. © 2011 by the authorsen
dc.description.abstractlicensee MDPI, Basel, Switzerland.en
dc.sourceMolBanken
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-80053079130&doi=10.3390%2fM728&partnerID=40&md5=f9df06d8af34237226ed8d68381c1202
dc.subjectBenzoxazineen
dc.subjectNS2028en
dc.subjectOxadiazoleen
dc.subjectSoluble guanylyl cyclase inhibitorsen
dc.subjectSuzuki-Miyaura couplingen
dc.title8-[2-Chloro-5-(trifluoromethyl)phenyl]-4H-[1,2,4]oxadiazolo-[3,4-c][1,4]benzoxazin-1-oneen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3390/M728
dc.description.volume2011
dc.description.issue2
dc.description.startingpage1
dc.description.endingpage4
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.gnosis.orcid0000-0002-4652-7567


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